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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1289904생성일: 2026년 10월 27일

Potassium Carbonate → (4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazide

https://huagongshe.com/reaction/1289904

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물(4S)-6-iodo-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indoleHCID 10691283—
반응물HCID 178516071HCID 178516071—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazideHCID 70284014—

반응 단계

To a solution of 5.0 g (13.1 mmol) of (4S)-6-iodo-4-(di-n-propylamino)-1,3,4, 5-tetrahydrobenz [cd] indole in 250 ml of acetonitrile was added 3.5 g (37 mmol) of 2-hydroxypyridine, 16.9 g (122 mmol) of powdered potassium carbonate, and 0.30 g (0.26 mmol) of tetrakis (triphenylphosphine)palladium. The resultant mixture was heated at 65° C. under a carbon monoxide atmosphere for 14 hours. The cooled mixture was then treated with 2 ml of hydrazine hydrate and stirred for another 15 hours. After filtering, the mixture was concentrated in vacuo to provide a residue. This residue was taken up in methylene chloride and extracted with aqueous tartaric acid solution. The aqueous layer was basified with 1M sodium hydroxide solution and the product was extracted into methylene chloride. Evaporation of solvent in vacuo left an oily solid which, after thorough washing with a 1:2 mixture of toluene and hexane, afforded 0.60 g of (4R)-4-(di-n-propylamino) -1,3,4,5-tetrahydrobenz [cd]indole-6-carboxylic hydrazide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750554
출처 데이터셋uspto-grants-1998_05
ORD IDord-850ae2fc655b41c3bc97d99377e9a07b
출처 메모uspto-grants-1998_05