関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | 4-Benzylmorpholine-2-carboxylic acid | HCID 2776353 | — |
| 反応物 | 2-Amino-1-(3-chlorophenyl)ethanone | HCID 3026272 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-[2-(3-Chlorophenyl)-2-oxoethyl]-4-(phenylmethyl)-2-morpholinecarboxamide | HCID 66990931 | 21.4% |
反応手順
Oxalyl chloride (1.32 mL, 15.03 mmol) was added to the suspension of 4-(phenylmethyl)-2-morpholinecarboxylic acid (2.218 g, 10.02 mmol) and DMF (0.155 mL, 2.005 mmol) in CH2Cl2 (100 mL) at 0° C. in 10 minutes, and the resulting mixture was stirred at 25° C. for 2 hours. The mixture was concentrated, and the resulting residue was dissolved in CH2Cl2 (100 mL) and triethylamine (3.07 mL, 22.05 mmol). 2-Amino-1-(3-chlorophenyl)ethanone (1.7 g, 10.02 mmol) was added to the brown solution at 0° C., and the reaction mixture was stirred at 25° C. for 3 hours. Water (150 mL) was added to the reaction mixture, and the aqueous mixture was extracted with EtOAc (3×100 mL). The combined organic layers were dried (Na2SO4), filtered, and evaporated. The resulting residue was purified by silica gel chromatography using as eluent 50% EtOAc in petroleum ether to afford the title compound (800 mg) as a pale yellow solid. LC-MS (ES) m/z=373 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08697685B2 |
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| 出典データセット | uspto-grants-2014_04 |
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| ORD ID | ord-dc534dcd9e8b4cacba077eac4215afda |
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| 出典メモ | uspto-grants-2014_04 |
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