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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35208생성일: 2026년 10월 23일

Ammonia → 3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylurea

https://huagongshe.com/ko/reaction/35208

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물LisurideHCID 28864—
반응물Sodium borohydrideHCID 4311764—
용매Trifluoroacetic acidHCID 6422—
생성물3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylureaHCID 8674234253.8%

반응 단계

At -20° C., 19.6 g of 3-(9,10-didehydro-6-methyl-8α-ergolinyl)-1,1-diethylurea is dissolved in 80 ml of trifluoroacetic acid, and 8 portions of respectively 500 mg of sodium borohydride are added at intervals of 3-4 minutes. The mixture is then poured on ice, made alkaline under ice cooling with 90 ml of 26% ammonia solution, and extracted with methylene chloride. The organic phase is dried, concentrated, and chromatographed on silica gel with methylene chloride/methanol, thus isolating 10.6 g of 3-(9,10-didehydro-2,3-dihydro-6-methyl-8α-ergolinyl)-1,1-diethylurea as a mixture of isomers of the 3α and 3β-H-compounds. Crystallization from ethyl acetate yields 6.5 g of the 3β-H-compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766128
출처 데이터셋uspto-grants-1988_08
ORD IDord-89628022f31d4c1cb80c087367553939
출처 메모uspto-grants-1988_08