関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | (1-Bromoethyl)benzene | HCID 11454 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | N-[5-cyano-2-(4-morpholinyl)-1,3-thiazol-4-yl]acetamide | HCID 66780286 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-[5-cyano-2-(4-morpholinyl)-1,3-thiazol-4-yl]-N-(1-phenylethyl)acetamide | HCID 66780432 | 84.9% |
反応手順
NaH (43.6 mg, 1.090 mmol) was added to a suspension of N-[5-cyano-2-(4-morpholinyl)-1,3-thiazol-4-yl]acetamide (250 mg, 0.991 mmol) in Tetrahydrofuran (THF) (8 mL) at 0° C. The resulting mixture was stirred at 0° C. for 10 min. (1-Bromoethyl)benzene (183 mg, 0.991 mmol) was added dropwise. N,N-Dimethylformamide (DMF) (2 mL) was added. The reaction mixture was heated at 50° C. overnight. LCMS showed the reaction was almost completed. EtOAc was added and washed with H2O, brine and dried (Na2SO4). Removal of the solvent followed by flash column chromatography on a 25 g silica column, which was eluted with 50% EtOAc/hexane to give 300 mg of light yellow sticky/foamy solid as the product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08410095B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-f2acc79ef5c34c2494aad2ae5239932e |
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| 出典メモ | uspto-grants-2013_04 |
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