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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1394110생성일: 2026년 10월 27일

2,6-Dichlorobenzaldehyde → 2-(2-Cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid [1-(2,6-dichlorobenzyl)-pyrrolidin-3-yl]methylamide

https://huagongshe.com/reaction/1394110

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DichlorobenzaldehydeHCID 6737—
반응물2-(2-Cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid (1-pyrrolidin-3-yl)methylamideHCID 86610307—
용매DichloromethaneHCID 6344—
생성물2-(2-Cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid [1-(2,6-dichlorobenzyl)-pyrrolidin-3-yl]methylamideHCID 86610306—

반응 단계

Compound 2-(2-cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid (1-pyrrolidin-3-yl)methylamide (1) (1.66 mmol) was dissolved in DCM (15 mL) under a blanket of nitrogen. 2,6-Dichlorobenzaldehyde (320 mg, 1.82 mmol) and sodium triacetoxyboron hydride (530 mg, 2.48 mmol) were added. The reaction mixture was stirred overnight at RT under a blanket of nitrogen. Following removal of the solvent in vacuo and purification by column chromatography (SiO2, DCM/MeOH 95:5), there were obtained 623 mg (1.11 mmol, 67% of theory) of the desired product 2-(2-cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid [1-(2,6-dichlorobenzyl)-pyrrolidin-3-yl]methylamide (K).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07348347B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-7efaa9714f4a492d82ea84182d668f1b
출처 메모uspto-grants-2008_03