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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232718생성일: 2026년 10월 26일

Benzaldehyde → 8-benzylamino-6-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/232718

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물8-amino-6-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-3,4-dihydrocarbostyrilHCID 23359071—
반응물HCID 178418435HCID 178418435—
용매EthanolHCID 702—
생성물8-benzylamino-6-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-3,4-dihydrocarbostyrilHCID 2335909965.5%

반응 단계

In 10 ml of ethanol was dissolved 1 g of 8-amino-6-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-3,4-dihydrocarbostyril. Thereto was added 0.3 g of benzaldehyde. The mixture was refluxed by heating, for 4 hours in an oil bath. The reaction mixture was allowed to cool and then mixed with 0.15 g of sodium boron hydride. The mixture was stirred at room temperature for 4 hours and subjected to distillation under reduced pressure to remove the solvent. The residue was mixed with water. The mixture was extracted with methylene chloride. The extract was dried with anhydrous sodium sulfate and subjected to distillation to remove the solvent. The residue was purified by silica gel column chromatography (elutant: methylene chloride/methanol=100/1~50/1~20/1). The eluate was subjected to distillation to remove the solvent. The residue was recrystallized from ethanol-n-hexane to obtain 0.8 g of 8-benzylamino-6-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-3,4-dihydrocarbostyril as a light yellow powder having a melting point of 144.5°-145.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591751
출처 데이터셋uspto-grants-1997_01
ORD IDord-436996e1799b4f9d88fd1db4c47d1188
출처 메모uspto-grants-1997_01