関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thiobenzamide | HCID 683563 | — |
| 反応物 | N-[2-(4-Bromoacetyl-phenyl)-ethyl]-acetamide | HCID 18523617 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-[2-[4-(2-Phenyl-thiazol-4-yl)-phenyl]-ethyl}-acetamide | HCID 9343045 | 100% |
反応手順
In a round-bottomed flask, thiobenzamide (357 mg, 2.60 mmol) and N-[2-(4-bromoacetyl-phenyl)-ethyl]-acetamide (740 mg, 2.60 mmol) were combined in ethanol (30 ml) and heated to about 80° C. for about three hours. The reaction mixture was then concentrated in vacuo to yield an off-white solid. The resulting material (838 mg, 100% yield) was ascertained to be pure by NMR and was carried into the next step directly without further purification. LRMS ([M+H]+)=323.2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06566377B2 |
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| 出典データセット | uspto-grants-2003_05 |
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| ORD ID | ord-81e17ae6d069429eace8613d4739982c |
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| 出典メモ | uspto-grants-2003_05 |
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