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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 126809생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → 5,5-Dimethyl-8-(3-methyl-2-octyl)-10-[4-(piperidino)butyryloxy]-5H-[1]benzopyrano[3,4-d]pyridine hydrochloride

https://huagongshe.com/ko/reaction/126809

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물4-(Piperidin-1-yl)butanoic acid hydrochlorideHCID 13172081—
반응물5,5-Dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridineHCID 19781402—
용매DichloromethaneHCID 6344—
생성물5,5-Dimethyl-8-(3-methyl-2-octyl)-10-[4-(piperidino)butyryloxy]-5H-[1]benzopyrano[3,4-d]pyridine hydrochlorideHCID 20287832—

반응 조건

온도5 °C

반응 단계

A mixture of 3.53 g. (0.01 mole) of 5,5-dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridine, 2.07 g. (0.01 mole) of γ-piperidinobutyric acid hydrochloride, 2.16 g. (0.0105 mole) of N,N'-dicyclohexylcarbodiimide, and 160 ml. of dried methylene chloride was stirred overnight at room temperature. The reaction mixture was cooled at approximately 5° C. for several hours and was filtered to remove dicyclohexylurea. The filtrate was evaporated in vacuo and the residue was dissolved in 12.5 ml. of methylene chloride and 50 ml. of cyclohexane. After standing overnight in the cold room (approximately 5° C.), the mixture was filtered again and the filtrate was evaporated in vacuo. The residue was recrystallized from methylene chloride/ether, giving 4.1 g. of the product, m.p. 134°-137°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254116
출처 데이터셋uspto-grants-1981_03
ORD IDord-d02bd2eb72254743b2fa2e02d4c6c99e
출처 메모uspto-grants-1981_03