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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2110001생성일: 2026년 10월 25일

Methanol → 2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2110001

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물3,5-DichlorosalicylaldehydeHCID 66660—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-[(piperidin-4-ylmethyl)-amino]-1H-benzimidazole-4-carboxylic acid methyl esterHCID 69067985—
용매Dimethylsulfoxide acetic acidHCID 18355466—
생성물2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl esterHCID 10195352—

반응 조건

온도50 °C

반응 단계

After dissolving 2-[(piperidin-4-ylmethyl)-amino]-1H-benzimidazole-4-carboxylic acid methyl ester (20 mg, 0.055 mmol) in dimethylsulfoxide-acetic acid (10:1), 2-hydroxy-3,5-dichlorobenzaldehyde (32.0 mg, 0.166 mmol) and sodium triacetoxyborohydride (35.0 mg, 0.166 mg) were added and the mixture was stirred at 50° C. for 2 days. Methanol (1 ml) was added to the reaction mixture, and then after stirring for 1 minute, it was purified by SCX solid phase extraction (Bond Elute SCX500MG). The product was further purified by preparative HPLC to obtain 2-{[1-(3,5-dichloro-2-hydroxy-benzyl)-piperidin-4-ylmethyl]-amino}-1H-benzimidazole-4-carboxylic acid methyl ester. The compound was identified by LC-MS.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517875B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-432aaa06404b40bea99d45bff01826f0
출처 메모uspto-grants-2009_04