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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227662생성일: 2026년 10월 26일

Potassium Carbonate → 2-(6-Fluoro-1H-benzimidazol-1-yl)-4-({[2-(trifluoromethyl)phenyl]methyl}oxy)-1,3-thiazole-5-carboxamide

https://huagongshe.com/reaction/227662

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-FluorobenzimidazoleHCID 235698—
반응물2-(1H-Benzimidazol-1-yl)-4-({[2-(trifluoromethyl)phenyl]methyl}-oxy)-1,3-thiazole-5-carboxamideHCID 11538969—
반응물2-Chloro-4-({[2-(trifluoromethyl)phenyl]methyl}oxy)-1,3-thiazole-5-carboxamideHCID 57756681—
용매DimethylformamideHCID 6228—
생성물2-(6-Fluoro-1H-benzimidazol-1-yl)-4-({[2-(trifluoromethyl)phenyl]methyl}oxy)-1,3-thiazole-5-carboxamideHCID 11704773—

반응 단계

Following the procedure described above for the preparation of 2-(1H-benzimidazol-1-yl)-4-({[2-(trifluoromethyl)phenyl]methyl}oxy)-1,3-thiazole-5-carboxamide using the following materials: 2-chloro-4-({[2-(trifluoromethyl)phenyl]methyl}oxy)-1,3-thiazole-5-carboxamide (0.050 g, 0.14 mmol), 5-fluorobenzimidazole (0.011 g, 0.08 mmol), K2CO3 (0.011 g, 0.08 mmol) and DMF (4 mL). Data for 6 regioisomers: 1H NMR (400 MHz, CDCl3) δ 8.46 (s, 1H), 7.82-7.74 (m, 2H), 7.69-7.58 (m, 3H), 7.54-7.50 (m, 1H), 7.16 (td, J=9.1, 2.4 Hz, 1H), 6.80 (bs, 1H), 5.82 (s, 2H), 5.76 (bs, 1H). MS m/z 437 (m+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560568B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-fe4511be6e774e46a857efc0d9271968
출처 메모uspto-grants-2009_07