Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống
1
/ 41 trang
THÔNG TIN TÀI LIỆU
Thông tin cơ bản
Định dạng
Số trang
41
Dung lượng
1,11 MB
Nội dung
I HC QUC GIA H NI TRNG I HC KHOA HC T NHIấN DNG THANH NGA TNG HP V TNH CHT CA MT S HP CHT 2, 4-DIHYDROXYQUINOLIN TH Cể CHA HP PHN NG LUN VN THC S KHOA HC Chuyờn ngnh: Húa Hu C Mó s : 60440114 H Ni 2017 I HC QUC GIA H NI TRNG I HC KHOA HC T NHIấN DNG THANH NGA TNG HP V TNH CHT CA MT S HP CHT 2, 4-DIHYDROXYQUINOLIN TH Cể CHA HP PHN NG LUN VN THC S KHOA HC Chuyờn ngnh : Húa Hu c Mó s :60440114 Cỏn b hng dn: GS TS Nguyn ỡnh Thnh H Ni - 2017 LI CM N hon thnh lun ny, trc tiờn cho em gi li cam n chõn tiGS TS Nguyn ỡnh Thnh a giao ti, tn tỡnhhng dnv ch bo em sut thi gian thc hin lun tt nghip Em cng xin chõn thnh cm n cỏc Thy, cụ b mụn Hoỏ Hu C, cỏc anh ch, cỏc bn v cỏc em phũng Tng Hp Hu C I ó luụn to iu kin, ng viờn, trao i v giỳp em hon thnh lun vntt nghip ny H Ni, thỏng nm 2017 Hc viờn Dng Thanh Nga [Type text] Page 59 CC K HIU VIT TT 13 : 13carbon C-Nuclear Magnetic Resonance (Ph cng hng t ht nhõn carbon-13) C NMR DMSO-d6 : Dimethyl sulfoxide c deuteri húa nc : im núng chy IR : Infrared Spectroscopy (Ph hng ngoi) MS : Mass Spectrometry (Ph lng) H NMR :1H-Nuclear Magnetic Resonance(Ph cng hng t ht nhõnproton) : chuyn dch húa hc [Type text] Page 59 DANH MC BNG BNG 3.1 Kt qu ph IR ca mt s hp cht 2-methylquinolin-4(1H)-on th 51 BNG 3.2 Kt qu ph IR ca mt s dn xut ca hp cht 2-methylquinolin-4(1H)-on th 55 BNG 3.3.Kt qu ph IR ca mt s dn xut ca hp cht 4-cloro-2-methylquinolin-4(1H)-on th 56 [Type text] Page 59 DANH MC HèNH Hỡnh 3.1.Ph IR ca 4-hydroxyquinolin-2-on 44 Hỡnh 3.2.Ph IR ca 4-hydroxy-7-methylquinolin-2-on 45 Hỡnh 3.3.Ph 1H NMR ca 4-hydroxy-7-methylquinolin-2-on 46 Hỡnh 3.4 Ph 13C NMR ca 4-hydroxy-7-methylquinolin-2-on .47 Hỡnh 3.5 Ph 1H NMR ca hp cht 4-propynyloxyquinolin-2(1H)-on 48 Hỡnh 3.6 Ph 1H NMR ca 7-methyl-4-propynyoxyquinolin-2-on .49 Hỡnh 3.7 Ph 13C NMR ca 7-methyl-4-propynyloxylquinolin-2-on .50 Hỡnh 3.8.Ph IR ca 2-methylquinolin-4-on 52 Hỡnh 3.9.Ph IR ca 2,8-dimethylquinolin-4(1H)-on 52 Hỡnh 3.10.Ph 1H NMR ca hp cht 2-methylquinolin-4(1H)-on 53 Hỡnh 3.11.Ph 13C NMR ca hp cht 2-methylquinolin-4(1H)-on .54 Hỡnh 3.12 Ph IR ca 2,8-dimethyl-4-cloroquinolin 55 Hỡnh 3.13 Ph IR ca hp cht 4-azido-2,8-dimethylquinolin 57 Hỡnh 3.14 Ph 1H NMR ca hp cht 4-azido-2,8-dimethylquinolin 58 Hỡnh 3.15 Ph 13C NMR ca hp cht 4-azido-2,8-dimethylquinolin .59 Hỡnh 3.16 Ph 1H NMR ca hp cht 4-azido-2,6-dimethylquinolin .60 Hỡnh 3.17 Ph 13C NMR ca hp cht 4-azido-2,6-dimethylquinolin 61 Hỡnh 3.18 Ph 1H NMR caPhn ng click gia 4-azido-2-methylquinolin vi propagyl Tetre-O-acetyl--Dglucopyranoside 63 Hỡnh 3.19 Ph C NMR caPhn ng click gia 4-azido-2-methylquinolin vi propagyl Tetre-O-acetyl--Dglucopyranoside 64 [Type text] Page 59 MC LC M U CHNG TNG QUAN 10 1.1 TNG QUAN V QUINOLIN 10 1.1.1 Gii thiu v quinolin 10 1.1.2 Tớnh cht ca quinolin 10 1.1.3 Tng hp quinolin 11 1.2 TNG QUAN V CC 2-METHYLQUINOLIN-4(1H)-ON TH 14 1.2.1 Gii thiu v cỏc 2-methylquinolin-4(1H)-on v dn xut 14 1.2.2 Tớnh cht húa hc 15 1.2.3 Phn ng tng hp 2-methylquinolin-4(1H)-on v dn xut 18 1.2.1 Hoat tớnh sinh hc 19 1.3 TễNG QUAN VấPHAN NG CLICK 20 1.3.1 Gii thiu 20 1.3.2 Tng quan tỡnh hỡnh nghiờn cu 21 1.4 Tng hp 4-hydroxyquinolin 27 1.4.1 Tng hp t ethyl oxaloacetate 27 1.4.2 Tng hp t ester ethyl ethoxylmethylenemalonic 28 1.4.3 Tng hp t hp cht thm ortho disubstituted 28 1.4.4 Tng hp t ethyl acetoacetat 29 CHNG PHN THC NGHIM Error! Bookmark not defined 2.1 TNG HP 2, 4-DIHYDROXYQUINOLIN THError! Bookmark not defined 2.1.1 Tng hp 2, 4-dihydroxyquinolin Error! Bookmark not defined 2.1.2 Tng hp 7-methyl-2,4-dihydroxyquinolinError! Bookmark not defined 2.2 TNG HP 4-PROPYNYLOXYQUINOLIN-2-ON THError! Bookmark not defi 2.2.1 Tng hp 4-propargyloxyquinolin-2-onError! Bookmark not defined 2.2.2 Tng hp 7-methyl-4-propargyloxyquinolin-2-onError! Bookmark not defined 2.3 TNG HP MT S HP CHT -ENAMIN CA ETHYL ANILINOCROTONATE TH Error! Bookmark not defined 2.4 TNG HP MT S HP CHT CA CC 2METHYLQUINOLIN-4-ON TH Error! Bookmark not defined 2.4.1 Tng hp 2-methylquinolin-4-on Error! Bookmark not defined [Type text] Page 59 2.4.2 Tng hp 2,8-dimethylquinolin-4-on Error! Bookmark not defined 2.4.3 Tng hp 2,6-dimethylquinolin-4-on Error! Bookmark not defined 2.4.4 Tng hp 8-methoxy-2-methylquinolin-4-onError! Bookmark not defined 2.5 TNG HP DN XUT 4-CLORO-2-METHYLQUINOLIN THError! Bookma 2.5.1 Tng hp 2-methy-4-clorolquinolin Error! Bookmark not defined 2.5.2 Tng hp 2,6-dimethyl-4-cloroquinolinError! Bookmark not defined 2.5.3 Tng hp 2,8-dimethyl-4-cloroquinolinError! Bookmark not defined 2.5.4 Tng hp 8-methoxyl-2-methyl-4-cloroquinolinError! Bookmark not defined 2.6 TNGHP CC 4-AZIDO-2-METHYL-QUINOLIN THError! Bookmark not d 2.6 Tng hp 4-azido-2-methylquinolin Error! Bookmark not defined 2.6.2 Tng hp 4-azido-2,8-dimethylquinolinError! Bookmark not defined 2.6.3 Tng hp 4-azido-2,6-dimethylquinolinError! Bookmark not defined 2.6 Tng hp 8-methoxy-4-azido-2-methylquinolinError! Bookmark not defined 2.7 PHN NG CLICK CA 4-AZIDO-2-METHYLQUINOLITH VI PROPARGYL TETRA-O-ACETYL--D-GLUCOPYRANOSIDEError! Bookmark not def Chng KT QU V THO LUN Error! Bookmark not defined 3.1 TNG HP 4-HYDROXYQUINOLIN-2(1H)-ON THError! Bookmark not define 3.1.1 Tng hp 4-hydroxyquinolin-2(1H)-onError! Bookmark not defined 3.1.2 Tng hp 4-hydroxy-7-methylquinolin-2(1H)-onError! Bookmark not defined 3.2 TNG HP MT S 4-PROPARGYLOXYQUINOLIN-2(1H)-ON TH Error! Bookmark not defined 3.2.1 Tng hp 4-propargyloxyquinolin-2-onError! Bookmark not defined 3.2.2 Tng hp 7-methyl-4-propargyloxyquinolin-2-onError! Bookmark not defined 3.3 TNG HP CC 2-METHYLQUINOLIN-4-ON THError! Bookmark not define 3.3.1 iu ch enamin Error! Bookmark not defined 3.3.2 Phn ng úng vũng cỏc enamin Error! Bookmark not defined 3.3.3 Ph hng ngoi ca cỏc hp cht ca 2-methylquinolon-4(1H)-on th Error! Bookmark not defined 3.3.4 Ph cng hng t ca cỏc hp cht ca 2-methylquinolon4(1H)-on thError! Bookmark 3.4 TNG HP MT S 4-CLORO-2-METHYLQUINOLINError! Bookmark not de 3.5 TNG HP MT S 4-AZIDO-2-METHYLQUINOLINError! Bookmark not def [Type text] Page 59 3.5.1 Ph hng ngoi cỏc dn sut ca cỏc hp cht ca 2-metylquinolon4(1H)-on th Error! Bookmark not defined 3.5.2.Ph cng hng t ca 4-azido-2,8-dimethylquinolinError! Bookmark not define 3.5.3 Ph cng hng t ca 4-azido-2,6-dimethylquinolinError! Bookmark not defin 3.6 PHN NG CLICK CA 4-AZIDO-2-METHYLQUINOLIN VI PROPAGYL TETRA-O-ACETYL--D-GLUCOPYRANOSIDEError! Bookmark not defin KT LUN TI LIU THAM KHO PH LC [Type text] Error! Bookmark not defined 30 Error! Bookmark not defined Page 59 M U T thi xa xa, ngi ta ó bit iu ch v s dng mt s hp cht hu c i sng nh: gim, cht mu hu c, ru ethylic Ngy cựng vi s phỏt trin manh m ca khoa hc k thut núi chung v húa hc núi riờng, húa hc v tng hp cỏc cht hu ccng ngy cng phỏt trin nhm tao cỏc hp cht phc v cho i sng ca ngi, c bit l cỏc hp cht cú hoat tớnh sinh hc cao i vi c th ngi v sinh vt Cỏc hp cht ny ngy cng tr nờn cú ý ngha quan trng v c ỏp dng vo lnh vc y hc cha tr cỏc cn bnh him nghốo, nõng cao sc khe cho ngi v ng vt Nh chỳng ta ó bit, quinolin-4(1H)-on l hp cht hu c i t dn xut ca quinolone vi hoat tớnh sinh hc cao Chng han nh chng viờm, khỏng nm, khỏng khun, cú thuc chng co git, gim au [6,17] Ngoi cỏc dn xut ca quinolone c s dng nh cht xỳc tỏc, cht c ch n mũn, cht bo qun õy cũn l hp cht trung gian quỏ trỡnh tng hp cỏc cht cú hoat tớnh sinh hc cao Chớnh vỡ vy hp cht ny ó c cỏc nh khoa hc nghiờn cu v gn thờm cỏc nhúm th khỏc c nhng hp cht cú hoat tớnh sinh hc a dang phong phỳ Mt s dn xut ca quinolone c phõn lp t thiờn nhiờn, hoc cng cú th tng hp theo phng phỏp tng hp ton phn Vi mc ớch gúp phn vo vic nghiờn cu v lnh vc húa hc ca cỏc monosaccharide cú cha d vũng, bn lun ny, em ó ó tin hnh nghiờn cu tng hp mt s dn xut ca 4-azido-2-methylquinolin, l hp cht chỡa khoỏ cho cỏc chuyn hoỏ tip theo thc hin mc ớch ny, lun thac s khoa hcca em ó thc hin mt s nhim v chớnh sau: + Tng hp mt s 2, 4-dihydroxyquinolin th + Tng hp mt s dn xut ca 2, 4-dihydroxyquinolin th + Tng hp mt s 2-methylquinolin-4-on th + Tng hp mt s dn xut ca2-methyl-4-cloroquinolin + Tng hp mt s dn xut ca 4-azido-2-methylquinolin [Type text] Page 59 50],hoc phn ng polymer hoỏ tng hp cỏc polymer mach thng di [49] Kiu cng hp vũng hoỏ 1,3-lng cc Huisgen trờn lai c phõn loai thnh cỏc loai sau: + Phn ng cng hp vũng hoỏ azide-alkyn c xỳc tỏc bng Cu(I) (CuAAC, Cu(I)-catalyzed Azide-Alkyne Cycloaddition) gia azide v alkyn tao thnh mt d vũng canh, 1,2,3-triazol th 1,4-di thay vỡ gm c ng phõn th 1,5-di phn ng cng hp 1,3-lng cc di tỏc dng ca nhit ca Huisgen N N N R R Đồng phân 1,4 N N R N R Đồng phân 1,5 + Phn ng cng hp vũng hoỏ azide-alkyn c xỳc tin bng sc cng vũng (SPAAC, Strain-promoted Azide-Alkyne Cycloaddition), phn ng loai ny, thay vỡ s dng Cu(I) hoat hoỏ alkyn, ngi ta s dng mt alkyn cú sc cng, nh difluorocyclooctyn, ú cỏc nhúm th gem-difluor hỳt electron manh v trớ propargylic hoat ng cựng vi sc cng vũng lm mt n nh ỏng k alkyn + Phn ng cng hp vũng hoỏ alkyn-nitron c xỳc tin bng sc cng vũng ca cỏc cyclooctyn th diaryl cú sc cng, bao gm dibenzylcyclooctyn (DIBO) ó c s dng phn ng vi cỏc 1,3-nitron (SPANC, Strain-promoted AlkyneNitrone Cycloaddition) cho cỏc N-alkyl isoxazolin [58] + Phn ng ca cỏc alken cú sc cng [59], chng han, cỏc trans-cycloalken (thng l cỏc cycloocten) v cỏc alken cú sc cng nh oxanorbornadien c s dng phn ng click vi mt s tỏc nhõn nh cỏc azide, tetrazin v tetrazol Loai phn ng ny bao hm s cng hp vũng hoỏ [3+2] ca alken v azide [61], phn ng Diels-Alder nghch o ca alken v tetrazin [62, 63] v phn ng photoclick ca alken v tetrazol [6468] Trong s cỏc kiu phn ng click tao d vũng 1,2,3-triazol thỡ phn ng ca cỏc alkyn u mach vi cỏc azide, c bit l cỏc azide hu c c cỏc nh [Type text] Page 59 tng hp hu c quan tõm bi vỡ s d dng xy ca phn ng vi hiu sut cao Ngoi cỏc hp cht kiu O-, S- v N-glucoside ca monosaccharide vi cỏc amin d vũng (indol, imidazol, quinolin, quinazolin, pyrimidin, pyridin, ) [6973], cỏc glycosylamin [74-78], v ó c quan tõm nghiờn cu c v mt lý thuyt cng nh thc nghim [79], thi gian gn õy ó cú mt s cụng b cp n phn ng click cỏc monosaccharide [25, 27],trong ú, natri azide c s dng lm hp phn azide thay vỡ azide hu c thụng thng, phn ng vi cỏc O-propargyl glycoside T nm 1999, húa hc click ó kớch thớch nhiu quan tõm cỏc lnh vc nghiờn cu khỏc nhau, c s dng nhiu lnh vc, t vi in t n vic gn nhón virus iu tr bnh ung th Mc dự nhu cu v vt liu húa cht mi v hoat tớnh sinh hc phõn t tip tc phỏt trin, cỏc nh húa hc ó hu nh khụng bt u khỏm phỏ cỏc úng gúp rng ln ca hp cht cú hoat tớnh [71].Trong bi cnh ca s yờu cu liờn tc v cỏc loai thuc tt hn thi gian ngn hn, nh húa y hc phi i mt vi nhim v khú khn ca vic tng hp cỏc phõn t mi, kt hp vi hoat tớnh cao v tớnh chn lc cao, ging thuc v cỏc tớnh cht dc lc tt Cỏc dc phm tim nng da trờn 1,2,3-triazol bao gm hp cht chng ung th CAI [72], dn xut nucleoside lm cht c ch enzyme chộp ngc, c gi l TSAO, [73] cỏc khỏng sinh -lactum Tazobactum, cephalosporine Cefatrizine (Hỡnh 1.2), v.v [Type text] Page 59 Hỡnh 1.2.Mt s dc phm tim nng trờn c s 1,2,3-triazol Ngc lai vi xu hng nghiờn cu ngy cng phỏt trin trờn th gii, Vit Nam, vic nghiờn cu phn ng click tng hp d vũng 1,2,3-triazol cha c cp n nhiu 1.4 Tng hp 4-hydroxyquinolin 1.4.1 Tng hp t ethyl oxaloacetate NH2 + H5C2OOC CH CO COOC 2H5 CH2Cl2 CH3COOH H5C2OOC CH Solution NH C COOC2H5 Jnert sovent 250o OH OH C N [Type text] CH CH OH- , -H2O C CH Heat N COOC 2H5 Page 59 Anilin ngng t vi ethyl oxaloacetate acid acetic loóng hoc dung dch methylene chloride tao -carbethoxyl--anilinoacerylate (2)(16) Sau ú úng vũng bng cỏch hn hp vo Dowtherm ó lm núng trc ú tao 4-hydroxy2-cacbethoxylquinolin, tip theo kh cacboxyl bng cỏch un núng bi Dowtherm nhit cao thu c 4-hydroxyquinolin 1.4.2 Tng hp t esterethyl ethoxylmethylenemalonic H5C6 NH2 + H5C2 O CH C (COOC 2H5)2 OH (H 5C2OOC) C NH 240-50oc CH N OH (COOC 2H5)2 CH i) OH- CH ii) -CO2 CH N CH Gould v Jocobs ó gii thiu ethyl ethoxylmethylenemalonic nh mt thnh phn -keto ester catng hp Conrad-Limpuch Tng hp ny sau ú thy phõn tao 4-hydroxyquinolin-3-carboxylic acid Sau ú l phn ng kh cacboxyl b un núng nhit cao 1.4.3 Tng hp t hp cht thm ortho disubstituted COOR OH ' OEt + R Ph Me OEt N C6H õy l loai tng hp dnh mt quinoline ca mt cu trỳc v õy l li th nht ca phng phỏp ny so vi cỏc loai khỏc ca phng phỏp Nhng nhc im ln ca loai hỡnh nyl khú khn ca synthesising cỏc vt liu Liementowski ó bỏo cỏo rng acid anthranilic un núng vi acetophenone tao 2-phenyl-4hydroxyquinoline Sn lng phn ng ny ớt v nú cú th c ci thin nuanthranilic acid v xeton c thay th ln lt bi methyl anthranilate v ketal ca keton Khi acid anthranilic ó c s dng v trớ ca ester "nng sut ó c xung vỡ cỏc phn ng kh carboxyl ca acid anthranilic theo cỏc iu kin [Type text] Page 59 ca phn ng Tuy vy s ngng t gia acid anthranilic v propiophenone tao 2phenyl-3-methyl- hydroxyquinoline cho nng sut cao hn 1.4.4 Tng hp t ethylacetoacetat OC 2H5 OC CH C NH re te om o r at tu era mp -H 2O NH2 + C2H5OH H O,H+ anhyd 130-40OC CaSO4 at 14 0-60 o C H3C COCH COOC 2H5 CH3 -C H OH H3C HO C CH CO NH Mt ester -keto nh ethylacetoacetat cú th phn ng vi amin thm bng mt hai cỏch nh hỡnh di õy cú kh nng ngng t nhit phũng nu thc hin vi s hin din ca mt acid Lm phỏt sinh mt cht xỳc tỏc Anil nu nú thc hin tai mc n im sụi tng ng ca hn hp phn ng an ton v anilide c hỡnh thnh anil (p -anilinocrotonic esterr) un núng n 240o-250oC mụi trng tr nh du hoc Dowtherm tao ra4-hydroxy-quinoline OH OC OC2H5 C NH -C2H5OH CH CH3 to CH N C CH3 Phn ng ny thng c gi l Conrad-Limpach Cỏc anilide v si m bng acid sulfuric m c v dnh mt dn xut 2hydroxyquinoline Phn ng ny l thng c gi l tng hp Knorrls Mt s ester S-keto khỏc ó c s dng Conrad-Limpach loai tng [Type text] Page 59 hp Trong s ny oxaloacetate ethyl v ethyl ethoxymethylenemalonate c c bit cp c s dng gn õy hn vic tng hp 2s3 ~ khụng th -4 - dn xut hydroxyquinoline cn thit cho vic tng hp aminoquinolines quan trng iu tr [Type text] Page 59 TI LIU THAM KHO Ting Vit 1.Nguyn ỡnh Thnh (2010), C s húa hc hu c, NXB hc Quc Gia H Ni, H Ni 2.Nguyn ỡnh Thnh (2011), Cỏcphng phỏp ph ng dng húa hc, NXB Khoa hc v K thut, H Ni 3.Nguyn Minh Tho (2001), Tng hp hu c, NXB hc Quc Gia H Ni, H Ni Nguyn Minh Tho (2001), Húa hc cỏc hp cht d vũng, NXB Giỏo dc, H Ni Trn Th Thu Thy, Ngụ Ngc Thng, inh Th H, Nguyn Quyt Chin, Stephanie Legoupy, Tng hp cỏc dn xut triazolo-cyclobutane nucleosidecú cha vũng piperazine, Tp Hoỏ hc,52(1) 19-23 (2014) Vng Vn Trng, Nghiờn cu chit tỏch v chuyn húa zerumbone mt s cõy thuc thuc h Gng (Zingiberaceae) Vit Nam v kho sỏt hot tớnh gõy c t bo ung th, Lun ỏn Tin s Hoỏ hc, H Ni (2016), 169 tr Ting Anh B Bhudevi, P Venkata Ramana, Anwita Mudiraj & A Ram Reddy(2009)Vol 48B, Synthesisof 4-hydroxy-3-formylideneamino-1H/methyl/phenylquinolin2-ones, Indian Journal of Chemistry, pp 255-260 Bhupendra Mistry , Smita Jauhari , (2010), Synthesis and characterization of some quinoline based azetidinones and thiazolidinones as antimicrobial agents, Archives of Applied Science Research 2(6), pp 332-343 Carla Prata, Nathalie Mora, Jean-Michel Lacombe, Jean-Claude Maurizis, Bernard Pucci, (1999), Synthesis and surface-active properties of glycosyl carbamates and thioureas, Carbohydrate Research 321(1-2), pp 4-14 El-hossain ali mohamed, (1991), On step synthesis of 4-hydroxycarbostyrils VI, Jour Chem Soc Pak Vol 13, pp 166-168 Farhalulah, Diptesh Sil, Brajendra K Tripathi, Arvi K Srivastava, (2004), Synthesis and glucose-6-phosphatase inhibitory activity of alkanoic acid [Type text] Page 59 esterrs, Bioorganic & Medicinal Chemistry Letters, 14(10), pp 2571-2574 10 Giorgos Athanasellis, Georgia Melagraki, Haralambos Chatzidakis, Antreas Afantitis, Anastasia Detsi, Olga Igglessi-Markopoulou, John Markopoulos, (2004), Novel Short-Step Synthesis of Funtionalized -Phenyl-hydroxybutenoates and their cyclization to 4-hydroxycoumarins via the Nhydroxybenzotriazole methodology, Synthesis11, pp 1775-1782 11.Li Qing-han , Zhao Zhi-gang , Chen Shu-hua , (2007) , Efficient synthesis of thiosemecarbasene under microwave irradiation, Chemical Research and Appication 9, pp 1011-1016 12.Li Z G , Wang Q M , Huang J M , (2001), The Preparation of Organic Intermediates, 2nd Ed, Chemical Industry Press, BeiJing, pp 66 13.Miguel Angel Alonso , J Ignacio Ubeda , Carmen Avendano , J CarlosMenendez , Mercedes Villacampa , (1993), New Findings on the Vilsmeier-Haack Approach to Quinoline derivatives, Tetrahedron 49(46), pp 10997-11008 14 Moaz M Abdou, (2014), Chemistry of 4-Hydroxy-2(1H)-quinolon Part 1: Synthesis and reactions, Arabian Journal of Chemistry, pp 1-13 15 Mohammad Mumtaz Alam , Akranth Marella , Mymoona Akhtar , Asif Husain , (2013), Microwave assisted on pot synthesis ofsome pyrazole derivatives as a safer anti-inflammatory and analgesic agents, Acta Polpniae Pharmaceutica- Drug Research 70(3), pp 435-441 16 Nevagi R J , Dhake A S , (2013), Antibacterial activity of thiosemicarbazide derivatives, Der Pharma Chemica 5(2), pp 45-49 17 Otero L , Vieites M , Boiani L , et al (2006), Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbasene complexes: DNA and redox metabolism as potential therapeutic targets, Journal of Medicinal Chemistry 49, pp 3322-3331 18 Shen Gu , Jean-Cristophe Brouet , Norton P Peet, and John D Williams , (2009), Survey of Solvents for the Conrad-Limpach Synthesis of 4Hydroxyquinolones, Synthetic Communications 39, pp 1563-1 19 W Dehaen, V.A Bakulev (Eds.), Chemistryof 1,2,3-triazoles, Springer International Publishing, Heidelberg,2015 [Type text] Page 59 20 A Lauria, R Delisi, F Mingoia, A Terenzi,A Martorana, G Barone, and A.M Almerico, 1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity,through 1,3-Dipolar Cycloadditions, Eur J Org Chem., 32893306 (2014) 21 F Fazio,M.C Bryan,O Blixt,J.C Paulson, andC.-H Wong, Synthesis of Sugar Arrays in Microtiter Plate, J Am Chem Soc., 124(48), 1439714402 (2002) B.H.M Kuijpers,S Groothuys,A.R Keereweer,P.J.L.M Quaedflieg,R.H Blaauw,F.L van Delft, andF.P.J.T Rutjes, Expedient Synthesis of Triazole-Linked Glycosyl Amino Acids and Peptides, Org Lett., 6(18), 31233126 (2004) 22 S Groothuys, B.H.M.Kuijpers,P.J.L.M Quaedflieg, H.C.P.F.Roelen, R.W.Wiertz, R.H.Blaauw, F.L.van Delft, F.P.J.T.Rutjes, Chemoenzymatic Synthesis of Triazole-Linked Glycopeptides, Synthesis, 18, 31463152 (2006) 23 Z.J Witczak,Monosaccharide Isothiocyanates: Synthesis, Chemistry, and Preparative Applications, In Advances in Carbohydrate Chemistry and Biochemistry, Academic Press Inc., Florida, Vol 44, 91-145 (1984) 24 H.S.G Beckmann and V Wittmann, In Organic Azides: Syntheses and Applications, S Brọse and K Banert, Ed., 2010, John Wiley & Sons, 469490 25 P Griess, Ueber eine neue Klasse organischer Verbindungen, in denen Wasserstoff durch Stickstoff vertreten ist, Justus Liebigs Annalen der Chemie, 137, 3991 (1866) 26 F Santoyo-Gonzỏlez, F Hernỏndez-Mateo, Azide-Alkyne 1,3-Dipolar Cycloadditions: a Valuable Tool in Carbohydrate Chemistry, Top Heterocycl Chem., 7, Springer-Verlag Berlin Heidelberg, 133177 (2007) 27 A Michael, Ueber die Einwirkung von Diazobenzolimid auf Acetylendicarbonsauremethylester,J Prakt Chem.,48, 94-95 (1893) 28 R Sustmann, H Trill, Substituent Effects in 1,3-Dipolar Cycloadditions of Phenyl Azide, Angew Chem Int Ed., 11, 838839 (1972) 29 H.C Kolb, M.G Finn, K.B Sharpless, Click Chemistry: Diverse Chemical [Type text] Page 59 Function from a Few Good Reactions, Angew Chem Int Ed 2001, 40, 20042021 30 V.V Rostovtsev, L.G Green, V.V Fokin, K.B Sharpless, A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective Ligation of Azides and Terminal Alkynes, Angew Chem Int Ed., 41, 25962599 (2002) 31 C.W Tornứe, C Christensen, M Meldal, Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal AlkynestoAzides, J Org Chem., 67, 30573064 (2002) 32 (a) V Wittmann, Glycopeptides and Glycoproteins: Synthesis, Structure, and Application, Springer-Verlag Berlin Heidelberg, 2007; (b) Hiroshi Kamitakahara, Ryo Suhara, Mao Yamagami, Haruko Kawano, Ryoko Okanishi,Tomoyuki Asahi, Toshiyuki Takano, A versatile pathway to end-functionalized cellulose ethers for clickchemistry applications, Carbohydr Polym., 151, 8895(2016) 33 R Huisgen, G Szeimies, L Moebius, 1,3-Dipolar Cycloadditions XXXII Kinetics of the Addition of Organic Azides to Carbon-carbon Multiple Bonds, Chem Ber.,100, 24942507 (1967) 34 R Huisgen, Centenary Lecture: 1,3-Dipolar Cycloaddtions, Proc Chem Soc., 357369 (1961); 1.3-Dipolare Cycloadditionen Rỹckschau und Ausblick, Angew Chem., 75, 60437 (1963); 1,3-Dipolar Cycloadditions Past and Future, Angew Chem Int Ed., 2, 565598 (1963) 35 A Padwa (Ed.), 1,3-Dipolar Cycloaddition Chemistry, John Wiley & Sons, Inc., New York, 1984 36 A Padwa, W.H Pearson (Eds.), Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Towards Heterocycles and Natural Products, John Wiley & Sons, Inc , New York, 2003 37 S Brọse, C Gil, K Knepper, V Zimmermann, Organic Azides: An Exploding Diversity of a Unique Class of Compounds, Angew Chem Int Ed., 44, 5188 [Type text] Page 59 5240 (2005) 38 E.F.V Scriven, K Turnbull, Azides: their preparation and synthetic uses, Chem Rev., 88, 297368 (1988) 39 E.F.V Scriven (Ed.), Azides and Nitrenes: Reactivity and Utility, Academic Press, Orlando, FL, USA, 1984 40 H.C Kolb, M.G Finn and K.B Sharpless, Click Chemistry: Diverse Chemical Function from a Few Good Reactions, Angew Chem Int Ed., 40, 20042021 (2001) 41 (a) A.P Rauter, T.K Lindhorst (Eds.), Carbohydrate Chemistry: Chemical and Biological Approaches, Volume 39, The Royal Society of Chemistry, Cambridge, UK, 2013; (b) V.K.Tiwari,B.B.Mishra,K.B.Mishra,N.Mishra,A.S.Singh, and X.Chen, Cu-Catalyzed Click Reaction in Carbohydrate Chemistry, Chem Rev., 116, 30863240 (2016) 42 J.P Horwitz, J Chua, The monomesylates of 1-(2-deoxy--D- lyxofuranosyl)thymines, Org Chem Ser Monogr.,29 (7), 2076-2079 (1964) 43 R Yarchoan, H Mitsuya, C Myers, S Broder, Clinical pharmacology of 3'azido-2',3'-dideoxythymidine (zidovudine) and related dideoxynucleosides, N Engl J Med., 321(11), 726-738 (1989) 44 M.A Da Rooge, M Noel, I.L Klundt, Nucleosides IX The Formation of 2',3'Unsaturated Pyrimidine Nucleosides via a Novel -Elimination Reaction, J Org Chem.,31(1), 205211 (1966) 45 (a) C.W Tornứe, M Meldal, Peptidotriazoles: Copper(I)-catalyzed 1,3-dipolar cycloadditions on solid-phase, Peptides 2001, Proc Am Pept Symp., American Peptide Society and Kluwer Academic Publishers, San Diego, 2001; pp 263264; (b) M.Meldal, and C.W.Tornứe,Cu-Catalyzed Azide-Alkyn Cycloaddition, Chem Rev., 108, 29523015 (2008) 46 A.E Speers, G.C Adam, B.F Cravatt, Activity-Based Protein Profiling in Vivo Using a Copper(I)-Catalyzed Azide-Alkyne [3+2] Cycloaddition, J Am Chem [Type text] Page 59 Soc., 125, 4686 4687 (2003) 47 K.E Beatty, F Xie, Q Wang, D A Tirrell, Selective Dye-Labeling of Newly Synthesized Proteins in Bacterial Cells, J Am Chem Soc., 127, 1415014151 (2005) 48 J.M Spruell, The Power of Click Chemistry for Molecular Machines and Surface Patterning, Doctoral Thesis, Northwestern University for Chemistry, Evanston, IL, USA, 2011 49 A Deiters, P.G Schultz, In vivo incorporation of an alkyne into proteins in Escherichia coli, Bioorg Med Chem Lett., 15, 15211524 (2005) 50 P.L Golas, N.V Tsarevsky, B.S Sumerlin, K Matyjaszewski, Catalyst Performance in Click Coupling Reactions of Polymers Prepared by ATRP: Ligand and Metal Effects, Macromolecules, 39, 64516457 (2006) 51 C.D Hein, X.-M Liu and D Wang, Click Chemistry, A Powerful Tool for Pharmaceutical Sciences, Pharm Res., 25,22162230 (2008) 52 R Huisgen 1,3-Dipolar cycloadditions Dipolare cycloadditionen Rỹckschau und Ausblick, Angew Chem., 75, 604637 (1963) 53 N.J Agard, J.M Baskin, J.A Prescher, A Lo and C.R Bertozzi, A Comparative Study of Bioorthogonal Reactions with Azides, ACS Chem Biol., 1, 644648 (2006) 54 J.A Codelli, J.M Baskin, N.J Agard, C.R Bertozzi, Second-Generation Difluorinated Cyclooctynes for Coptetra-Free Click Chemistry, J Am Chem Soc.,130, 1148611493 (2008) 55 X Ning, J Guo, M.A Wolfert, G.-J Boons, Visualizing metabolically labeled glycoconjugates of living cells by coptetra-free and fast huisgen cycloadditions, Angew Chem Int Ed.,47, 22532255 (2008) 56 C.G Gordon, J.L Mackey, J.C Jewett, E.M Sletten, K.N Houk, C.R Bertozzi, Reactivity of Biarylazacyclooctynones in Coptetra-Free Click Chemistry, J Am Chem Soc., 134, 9199 (2012) [Type text] Page 59 57 D.A MacKenzie, A.R Sherratt, M Chigrinova, L.L Cheung, J.P Pezacki, Strain-promoted cycloadditions involving nitrones and alkynesrapid tunable reactions for bioorthogonal labeling, Curr Opin Chem Biol., 21, 8188 (2014) 58 K Lang and J Chin, Bioorthogonal Reactions for Labeling Proteins, ACS Chem Biol., 9, 1620 (2014) 59 D.A MacKenzie, J.P Pezacki, Kinetics studies of rapid strain- promoted [3+2] cycloadditions of nitrones with bicyclo[6.1.0]nonyne, Can J Chem., 92, 337340 (2014) 60 S.S van Berkel,A.T.J Dirks, S.A Meeuwissen,D.L.L Pingen, O.C Boerman, P Laverman, F.L van Delft, J.J.L.M Cornelissen, F.P.J.T Rutjes, Application of Metal-Free Triazole Formation in the Synthesis of Cyclic RGDDTPA Conjugates,ChemBioChem, 9, 18051815 (2008) 61 F Liu, R.S Paton, S Kim, Y Liang, and K.N Houk, Diels-Alder Reactivities of Strained and Unstrained Cycloalkenes with Normal and Inverse-ElectronDemand- Dienes: Activation Barriers and Distortion/Interaction Analysis,J Am Chem Soc., 135, 1564215649 (2013) 62 U Rieder, N.W Luedtke, Alkene-tetrazine ligation for imaging cellular DNA,Angew Chem Int Ed Engl., 53, 91689172 (2014) 63 J.S Clovis, A Eckell, R Huisgen, R Sustmann, 1.3-Dipolare Cycloadditionen XXV.Der Nachweis des freien Diphenylnitrilimins als Zwischenstufe bei Cycloadditionen Chem Ber., 100, 6070 (1967) 64 S.S van Berkel, A.J Dirks,M.F Debets, F.L van Delft,J.J.L.M Cornelissen, R.J.M Nolte, andF.P.J.T Rutjes, Metal-Free Triazole Formation as aTool for Bioconjugation, ChemBioChem, 8, 15041508 (2007) 65 Z Yu, L.Y Ho, and Q Lin, Rapid, Photoactivatable Turn-On Fluorescent Probes Based on an Intramolecular Photoclick Reaction, J Am Chem Soc., 133, 1191211915 (2011) 66 Z Li, L Qian, L Li, J.C Bernhammer, H.V Huynh, J.S Lee, S.Q Yao, [Type text] Page 59 Tetrazole Photoclick Chemistry: Reinvestigating Its Suitability as a Bioorthogonal Reaction and Potential Applications, Angew Chem Int Ed Engl., 55, 20022006 (2016) 67 C.P Ramil, Q Lin, Photoclick chemistry: a fluorogenic light-triggered in vivo ligation reaction, Curr Opin Chem Biol., 21, 8995 (2014) 68 A Gursoy, B Unal, N Karali, G Otuk, Synthesis, Characterization and Primary Antimicrobial Activity Evaluation of 3-Phenyl-6-methyl-4(3H)- quinazolinone-2-yl-mercaptoacetic Acid Arylidenehydrazides, Turk J Chem., 29, 233-245 (2005) 69 J Isac-Garcớa, F Hernỏndez-Mateo, F.G Calvo-Flores, and F.SantoyoGonzỏlez, Reactivity of 2-Deoxy-2-iodoglycosyl Isothiocyanates with O-, S, and N-Nucleophiles Synthesis of Glycopyranoso-Fused Thiazoles, J Org Chem., 69, pp 202-205 (2005) 70 Mohamed A Saleh, Youssef A Abbas, Fouad Eadel-Hai, and Shaban A Youssef, Synthesis and Antiviral Evaluation of N-Glycosides derived from 6amino-3-Aryl-2-Methyl-4-(3H)-Quinazolinone, Nucleos Nucleot Nucl., 20 (10 & 11), 1891-1902 (2001) 71 Y.-H Liu, L.-H Cao, Synthesis and bioactivity of novel methyl 6-deoxy-6-(Nalkyl/aryl-N-benzothiazol-2-yl)guanidino--D-glucopyranosides, Carbohydr Res., 343, 615-625 (2008) 72 R Bognỏr, L Somogyi, L Szilỏgyi, Z Gyửrgydeỏk, N-Glykosyl-Derivate : Teil XIII Der nachtrọgliche ausbau des aglykons Synthese von N-Glykosyl-Derivaten des 2-amino-thiazoles, 2-amino-1,3,4-thiadiazoles und 5-amino-1,2,3,4- thiatriazols, Carbohydr Res., 5(3), 320-328 (1967) 73 F Damkaci and P DeShong, Stereoselective Synthesis of - and -7 Glycosylamide Derivatives from Glycopyranosyl Azides via Isoxazoline Intermediates, J Am Chem Soc., 125, (2003), pp 4408-4409 74 C L Perrin and J Kuperman, Anomeric Effects versus Steric Hindrance to [Type text] Page 59 Ionic Solvation in Protonated Glucosylanilines and Cyclohexylanilines, J Am Chem Soc., 125, (2003), pp 8846-8851 75 A Asnani, F.-I Auzanneau, Synthesis of Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively, Carbohydr Res., 338, 10451054 (2003) 76 J Li, S Zacharek, X Chen, J Wang, W Zhang, A Janczuk and P.G Wang, Bacteria Targeted By Human Natural Antibodies Using -Gal Conjugated Receptor-specific Glycopolymers, Bioorg Med Chem., 7, 1549-1558 (1999) 77 S.K Shinjo, I.L.S Tersariol, V Oliveira, C.R Nakaie, M.E.M Oshiro, A.T Ferreira, I.A Santos, C.P Dietrich, and H.B Nader, Heparin and Heparan Sulfate Disaccharides Bind to the Exchanger Inhibitor Peptide Region of Na+/Ca2+ Exchanger and Reduce the Cytosolic Calcium of Smooth Muscle Cell Lines, requirement of C4-C5 unsaturation and 14 glycosidic linkage for activity, J Biol Chem., 277(50), 48227-48233 (2002) 78 Zh.-Q Yang, E.B Puffer, J.K Pontrello, and L.L Kiessling, Synthesis of a multivalent display of a CD22-binding trisaccharide, Carbohydr Res., 337 (2002), pp 16051613 79 Nguyen Dinh Thanh, Nguyen Thi Thanh Mai, Synthesis of N-tetra-O-acetyl-D-glucopyranosyl-N-(4,6-diarylpyrimidine-2-yl)thioureas, Carbohydr Res., 344, 23992405 (2009) [Type text] Page 59 ... Sự cộng hợp vào liên kết bội carbon-carbon R R X [X] R R + Sản phẩm phụ (X = O, NR,+SR,+NR) (Sự tạo thành vòng ba cạnh) EWG EWG EWG + EWG EWG EWG (EWG: Nhóm hút electron) (Một số cộng hợp Michael)... not defined 2.1 TNG HP 2, 4 -DIHYDROXYQUINOLIN THError! Bookmark not defined 2.1.1 Tng hp 2, 4 -dihydroxyquinolin Error! Bookmark not defined 2.1.2 Tng hp 7-methyl -2,4- dihydroxyquinolinError! Bookmark... mt, khoa hc vt liu, cụng ngh nano [55-57] [Type text] Page 59 Sự cộng hợp vòng hoá R N N N + R R Cu(I) CH N N N R (Sự cộng hợp vòng hoá 1,3-lưỡng cực azide alkyn cuối mạch) Sự m vòng nucleophil