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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344393생성일: 2026년 10월 23일

Benzaldehyde → 4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamide

https://huagongshe.com/ko/reaction/344393

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물4-Amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamideHCID 54008363—
용매EthanolHCID 702—
생성물4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamideHCID 5401549672%

반응 단계

Benzaldehyde (0.76 g) was added to a solution of 4-amino-N-(1-(5-aminopentyl)piperidin-4-ylmethyl)-5-chloro-2-methoxybenzamide (2.0 g) in ethanol (50 ml), and the mixture was stirred at refluxing temperature for 3 hr. Sodium borohydride (0.53 g) was added to the reaction mixture under ice-cooling, and the mixture was stirred overnight at room temperature. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol:ammonia=50:5:1) to give 1.78 g of 4-amino-N-((1-(5-benzylaminopentyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05864039
출처 데이터셋uspto-grants-1999_01
ORD IDord-d8d6108f1b35472588e42ea8e4f89e05
출처 메모uspto-grants-1999_01