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1-Pyrrolidineethanamine → 3-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Pyrrolidineethanamine | HCID 1344 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-Bromobenzoic acid | HCID 11456 | — |
| 反応物 | Diethyl cyanophosphonate | HCID 76257 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamide | HCID 848685 | 85.4% |
反応手順
1-(2-Aminoethyl)pyrrolidine (4.34 g), diethyl cyanophosphate (5.57 ml) and triethylamine (10.4 ml) were added to a solution of 3-bromobenzoic acid (5.00 g) in N,N-dimethylformamide (DMF; 60 ml), and the mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with water and then extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residues were crystallized from hexane to give the title compound (6.31 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091247B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-20bfb9c6c3334504a550ae3aff9a8c0e |
| 出典メモ | uspto-grants-2006_08 |