참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 4-Bromopyrazole | HCID 16375 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [2-(4-Bromopyrazol-1-yl)ethyl]dimethylamine | HCID 21859709 | — |
반응 단계
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
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08697725B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_04 |
|---|
| ORD ID | ord-360eede0cf3640b6bd1a848cd1891ae6 |
|---|
| 출처 메모 | uspto-grants-2014_04 |
|---|