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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27083생성일: 2026년 10월 23일

Butyric Acid → 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole

https://huagongshe.com/ko/reaction/27083

반응식

참여 물질

역할이름HCID투입량
반응물Butyric AcidHCID 264—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물RP 35489HCID 3085171—
용매DichloromethaneHCID 6344—
생성물5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrroleHCID 1372862767.8%

반응 조건

온도20 °C

반응 단계

Butyric acid (0.71 g.) is added to a suspension of 6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-5-(piperazin-1-yl)carbonyloxy-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (2.50 g.) and N,N'-dicyclohexyl-carbodiimide (1.67 g.) in anhydrous methylene chloride (50 cc.) and the mixture is stirred for 1 hour at 20° C. After filtering off the dicyclohexylurea formed, washing with methylene chloride (15 cc.) and evaporating the solvent, the residue obtained (3.8 g.) is washed with boiling ethanol (35 cc.) and then recrystallised from a mixture of acetonitrile (110 cc.) and ethanol (11 cc.). 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (1.95 g.), which melts at 248° C., is thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220646
출처 데이터셋uspto-grants-1980_09
ORD IDord-156be8bfd6dc4e69a16089b33f19744f
출처 메모uspto-grants-1980_09