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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78497생성일: 2026년 10월 25일

5-Chloro-o-anisic acid → 5-chloro-N-(5-chlorothiazol-2-yl)-2-methoxybenzamide

https://huagongshe.com/reaction/78497

반응식

참여 물질

역할이름HCID투입량
반응물5-Chloro-o-anisic acidHCID 76970—
반응물2-Amino-5-chlorothiazole hydrochlorideHCID 148743—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
생성물5-chloro-N-(5-chlorothiazol-2-yl)-2-methoxybenzamideHCID 86618912—

반응 단계

A mixture of 2-amino-5-chlorothiazole hydrochloric acid (1.0 g, 5.9 mmol), 5-chloro-2-methoxybenzoic acid (1.3 g, 7.0 mmol), 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (Chem-Impex International, 2.2 g, 12 mmol), 1-hydroxbenzotriazole (0.95 g, 7.0 mmol) and 4-dimethylaminopyridine (0.14 g, 1.2 mmol) in 6 mL of pyridine was allowed to stir at ambient temperature for 72 hours. The reaction mixture was concentrated under reduced pressure and 10 mL of H2O was added. The resulting solids were isolated by filtration, washed with 5 mL of H2O and twice with 5 mL of ethyl acetate, and dried to afford the title compound. MS (DCI/NH3) m/z 303 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841334B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-16f7c185f4ca43919749ba8193650962
출처 메모uspto-grants-2014_09