化工社化工社 化学情報印刷レポート · 研究参考用
1,2-Dichloroethane → 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | Citric Acid | HCID 311 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | HOAt | HCID 181649 | — |
| 反応物 | 4-Carboxy-3-fluorophenylboronic acid | HCID 2763201 | — |
| 反応物 | 2,2-Difluoro-1-phenylethan-1-amine | HCID 45282641 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid | HCID 123534983 | — |
反応手順
To a solution of 4-borono-2-fluorobenzoic acid (200 mg, 1.087 mmol), 2,2-difluoro-1-phenylethanamine (232 mg, 1.196 mmol), and DIEA (0.570 mL, 3.26 mmol) in THF (3.866 mL) and DMF (0.483 mL) was added HOAt (296 mg, 2.175 mmol) and EDC (521 mg, 2.72 mmol). After 3 h stirring at room temperature, 10% citric acid solution was added (pH ˜3) and extracted with 2-methyl THF and EtOAc (1:1). The organic layers were dried over anhydrous Na2SO4, filtered, and concentrated. The crude 4-(2,2-difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid was obtained (90%) and used for the next step without purification. LCMS (m/z): 375.3 (MH+), 0.48 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09242996B2 |
| 出典データセット | uspto-grants-2016_01 |
| ORD ID | ord-10da6daac0da476486f9959ec4a2ca54 |
| 出典メモ | uspto-grants-2016_01 |