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Triethylamine → Tert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Amino-3-fluorobenzoic acid | HCID 9971 | — |
| 反応物 | Propylphosphonic anhydride | HCID 111923 | — |
| 反応物 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Tert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate | HCID 58055815 | 91.7% |
反応手順
To a stirred solution of 4-amino-3-fluorobenzoic acid (4.97 g, 32.04 mmol), tert-butyl piperazine-1-carboxylate (5.97 g, 32.04 mmol) and triethylamine (10 mL) in dichloromethane (100 mL) was added 1-propanephosphonic acid cyclic anhydride (20 mL, 50% solution in ethyl acetate, dropwise). The reaction mixture was stirred for 1 hour then was diluted with ethyl acetate, washed with potassium carbonate (aqueous), dried (magnesium sulfate) and concentrated under reduced pressure to give the title compound (9.5 g). MS (ESI) m/z: 324.5 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08759352B2 |
| 出典データセット | uspto-grants-2014_06 |
| ORD ID | ord-64ce207decc04c1aa951166ab423390d |
| 出典メモ | uspto-grants-2014_06 |