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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55351생성일: 2026년 10월 24일

(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazide → (-)(4R)-6-(5-phenyl-1,3,4-oxadiazol-2yl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole

https://huagongshe.com/ko/reaction/55351

반응식

참여 물질

역할이름HCID투입량
반응물(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazideHCID 70284014—
용매DichloromethaneHCID 6344—
용매Trimethyl orthobeznoateHCID 69720—
생성물(-)(4R)-6-(5-phenyl-1,3,4-oxadiazol-2yl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indoleHCID 22868970163.9%

반응 단계

A solution of 0.20 g (0.64 mmol) of (4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6-carboxylic hydrazide in 2.0 ml of trimethylorthobenzoate was heated at 135° C. under nitrogen for 5 hours. After cooling, the semisolid mixture was dissolved in methylene chloride and the product was extracted into aqueous tartaric acid. The aqueous solution was basified with sodium carbonate and the product was extracted into methylene chloride. Evaporation of the methylene chloride left crystalline product which was then chromatographed over 3 g of silica gel using ethyl acetate as eluent. The product from the column was recrystallized from toluene to give 0.21 g of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624944
출처 데이터셋uspto-grants-1997_04
ORD IDord-caa328d5a9ed459587c9da23d001ab2e
출처 메모uspto-grants-1997_04