Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → 3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylurea
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Lisuride | HCID 28864 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 생성물 | 3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylurea | HCID 86742342 | 53.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04766128 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-89628022f31d4c1cb80c087367553939 |
| 출처 메모 | uspto-grants-1988_08 |