참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Ethyl formate | HCID 8025 | — |
| 반응물 | Lisuride | HCID 28864 | — |
| 반응물 | 1,1-Ethanedithiol | HCID 33645 | — |
| 촉매 | Titanium Tetrachloride | HCID 24193 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3-[9,10-Didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]-1,1-diethylurea | HCID 86742055 | 12% |
반응 단계
Under argon, 11.5 g (0.03 mol) of 3-(9,10-didehydro-6-methyl-8α-ergolinyl)-1,1-diethylurea is dissolved in 300 ml of chloroform. At room temperature, 105 ml of ethyl formate and 5.4 ml of ethanedithiol are added in succession. Then 13.2 ml of titanium(IV) chloride in 150 ml of chloroform is added dropwise. The mixture is agitated for 3 days at room temperature. To work up the mixture, it is cooled in an ice bath and 75 ml of methanol and 600 ml of water are added in sequence dropwise to this mixture. The solution is rendered alkaline with 60 ml of 25% ammonia solution and extracted with methylene chloride. The organic phases are washed with water and dried over magnesium sulfate. The concentrated residue is chromatographed under pressure on silica gel with ethyl acetate/methanol 95:5, thus isolating 1.7 g of 3-[9,10-didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8α-ergolinyl]-1,1-diethylurea (12% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04847262 |
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| 출처 데이터셋 | uspto-grants-1989_07 |
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| ORD ID | ord-0bd8e2a6c5414cce8d6f8ddc70fc0fb6 |
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| 출처 메모 | uspto-grants-1989_07 |
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