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1,4-Diacetylbenzene → 1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Diacetylbenzene | HCID 13888 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Carbonyl bromide | HCID 79057 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanone | HCID 86616431 | — |
反応手順
A solution of 1-(4-Acetyl-phenyl)-ethanone (8.1 g, 5 mmol), in HOAc (50 mL) at 60° C. was treated with bromine (1 eq., 0.26 mL) dropwise over 10 minutes. After 5 more minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get drive off the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (30 mL) with NaOAc (1.1 g) and thiourea (1 eq., 375 mg) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the resulting mixture was redissolved in 5 ml of 90% DMF, 10% water with 0.1% TFA and purified by reverse phase HPLC to give the product. MS: 219.1 (M+H−).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07595398B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-bf1e3eb4baff409c84040f25d0325913 |
| 出典メモ | uspto-grants-2009_09 |