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HRID 1352371作成日:2026年10月27日
Dibromodifluoromethane → 4-[5-(2,2-Difluoro-vinyl)-thiazol-2-yl]-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1352371
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dibromodifluoromethane | HCID 6382 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Tert-butyl 4-(5-formyl-1,3-thiazol-2-yl)piperazine-1-carboxylate | HCID 23560811 | — |
| 触媒 | Zinc | HCID 23994 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-[5-(2,2-Difluoro-vinyl)-thiazol-2-yl]-piperazine-1-carboxylic acid tert-butyl ester | HCID 67549547 | 19% |
反応手順
To a solution of 6.73 mmol triphenylphosphine in 13 ml N,N-dimethylformamide was added 6.73 mmol dibromodifluoromethane and the mixture was stirred at room temperature for 1 h. 3.36 mmol 4-(5-formyl-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester was added and the mixture was then cooled to 0° C. 6.73 mmol zinc dust was added in small portions and stirring continued for 10 min at 0° C. The mixture was then allowed to warm to room temperature and stirring continued for a further 2 h. The reaction mixture was then filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography (SiO2, ethyl acetate/heptane) to afford the title compound as a white crystalline solid (yield 19%). MS (m/e): 332.3 (M+H+, 10%), 276.0 ([M+2H−tBu]+, 100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07220744B2 |
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| 出典データセット | uspto-grants-2007_05 |
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| ORD ID | ord-893b7398074045f48b844b52356d1857 |
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| 出典メモ | uspto-grants-2007_05 |
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