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Bromodiphenylmethane → 2-[4-[3-(Diphenylmethoxy)propyl]-1-piperazinyl]pyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Bromodiphenylmethane | HCID 236603 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 1-(2-Pyrimidinyl)-4-piperazinyl propanol | HCID 21279254 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-[4-[3-(Diphenylmethoxy)propyl]-1-piperazinyl]pyrimidine | HCID 14233954 | 26% |
反応手順
To a stirred solution of 1-(2-pyrimidinyl)-4-piperazinyl propanol 3 g. (0.013 mol) in 50 mol. of dimethylformamide was added 3.3 g. (0.013 mol) of diphenylmethylbromide and 2.9 g. (0.034 mol) of sodium bicarbonate. The reaction mixture was refluxed overnight, dimethylformamide was evaporated under reduced pressure, and the residue was extracted with methylene chloride (400 ml.). The methylene chloride extracts were collected, washed with water and evaporated, and the remaining residue was purified by HPLC to give 1.3 g. (26% yield) of the title compound. The free base which was converted to the (1:1) fumarate salt; m.p 166°-168° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04766215 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-db1c7b5655734fdd82605a2897516b93 |
| 出典メモ | uspto-grants-1988_08 |