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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1785520생성일: 2026년 10월 26일

Thiophene-2-carbohydrazide → thiophene-2-carboxylic acid N'-[4-(3-chloro-phenyl)-2-(5,6-dimethoxy benzoimidazol-1-yl)-thiazole-5-carbonyl]-hydrazide

https://huagongshe.com/reaction/1785520

반응식

참여 물질

역할이름HCID투입량
반응물Thiophene-2-carbohydrazideHCID 73098—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4-(3-Chloro-phenyl)-2-(5,6-dimethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acidHCID 23654019—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물thiophene-2-carboxylic acid N'-[4-(3-chloro-phenyl)-2-(5,6-dimethoxy benzoimidazol-1-yl)-thiazole-5-carbonyl]-hydrazideHCID 5759585070.2%

반응 단계

To a solution of 4-(3-Chloro-phenyl)-2-(5,6-dimethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid (41 mg, 0.1 mmol) and thiophene-2-carboxylic acid hydrazide (14.2 mg, 0.1 mmol, Aldrich) in N,N-dimethylformamide (1 ml) was added HATU (38 mg, 0.1 mmol) and diisopropylethylamine (26 μl, 0.15 mmol). The mixture was stirred at ambient temperature overnight. The solvent was reduced in vacuo and water (3 ml) was added. After sonication, the crude was filtered and sent directly for purification with prep-HPLC to afford thiophene-2-carboxylic acid N′-[4-(3-chloro-phenyl)-2-(5,6-dimethoxy benzoimidazol-1-yl)-thiazole-5-carbonyl]-hydrazide (37.9 mg, 70.2%) as a white solid. MS m/z 540 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07504513B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-79c97d7eb5cf42ed9c08b38a0ff2f9fc
출처 메모uspto-grants-2009_03