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Ammonia → 3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylurea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Lisuride | HCID 28864 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | 3-(9,10-Didehydro-2,3-dihydro-6-methyl-8alpha-ergolinyl)-1,1-diethylurea | HCID 86742342 | 53.8% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04766128 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-89628022f31d4c1cb80c087367553939 |
| 出典メモ | uspto-grants-1988_08 |