1-(4-Chlorobutanoyl)-3-(2-chlorophenyl)thiourea

روشهای جدید سنتز مشتقات تیازولو [b, 2, 3] [4, 2, 1] تری آزول و 1، 2، -4 تری آزولو [b -4, 3] [4, 3, 2] تیادین آذین

واکنش -3 مرکاپتو- 1، 2، -4 تری آزول های (i) با پروپارژیل برمید، -3 پروپارژیل مرکاپتو - 1، 2، -4 تری آزول های (ii) را ایجاد نمود. ترکیبات (ii) در حضور باز قوی و یا اسید قوی به ترکیبات -5متیل - تیازولو [b-2, 3] [4, 2, 1] تری آزول های (iii) تبدیل شدند. واکنش -4آمینو- -3مرکاپتو - -5فنیل - 1، 2، -4 تری آزول (iv) با پروپارژیل برمید، -4 آمینو - -3پروپارژیل مرکاپتو - -5فنیل - 1، 2، -4 تری آزول (v) را ا...

Synthesis and Antimicrobial Activity of Some 2-[(4-Substituted-Phenyl-3-Chloro-Azetidin-2-One)-5-(2'-Methylamino-4-Phenyl-1', 3'-Thiazolyl-]-1, 3,4-Thiadiazoles

A new 2-[(4-substituted-phenyl-3-chloroazetidin-2-one)-5-(2'-methylamino 4-phenyl-1', 3'-thiazolyl-]-1, 3, 4-thiadiazoles, 5(a-n) were synthesized from 2-substituted-benzylideneamino-5-[2'-methylamino-4'-phenyl-1',3'-thiazolyl]-1,3, 4-thiadiazole, 4(a-n) using 2-amino-4phenyl-1, 3-thiazole as a starting material. The synthesised compounds have been screened in vitro for their antimicrobial acti...

Synthesis and Leishmanicidal Activity of 1-[5-(5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl]-4-benzoylepiperazines

A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...

Synthesis and Leishmanicidal Activity of 1-[5-(5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl]-4-benzoylepiperazines

A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...

3 2 1 0 4 3 2