関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylamine | HCID 674 | — |
| 反応物 | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Bromopyrazole | HCID 16375 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | [2-(4-Bromopyrazol-1-yl)ethyl]dimethylamine | HCID 21859709 | — |
反応手順
4-bromopyrazole (100 mg, 0.680 mmol, available from Aldrich), cesium carbonate (333 mg, 1.021 mmol) and 1-bromo-2-chloroethane (0.085 mL, 1.021 mmol, available from Aldrich) were suspended in N,N-Dimethylformamide (DMF) (2 mL) and heated to 60° C. under microwave conditions in a Biotage Initiator for 1 hour. 2M dimethylamine in THF (1.701 mL, 3.40 mmol) added and the mixture allowed to stand over the weekend. The mixture was heated to 60° C. under microwave conditions in a Biotage Initiator for 1 hour, then to 100° C. under microwave conditions in a Biotage Initiator for 2 hours. The mixture was filtered, evaporated to 13 mbar, loaded on to a 5 g SCX cartridge and eluted with MeOH (25 ml) followed by 2M methanolic ammonia (25 ml). The basic fraction was evaporated to a colourless oil (99 mg). LCMS (Method C): Rt=0.43, MH+=218
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08697725B2 |
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| 出典データセット | uspto-grants-2014_04 |
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| ORD ID | ord-360eede0cf3640b6bd1a848cd1891ae6 |
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| 出典メモ | uspto-grants-2014_04 |
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