関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Bromouracil | HCID 5802 | — |
| 反応物 | 2-(Bromomethyl)-1,3-difluorobenzene | HCID 581435 | — |
| 反応物 | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | Urea, (2,6-difluorobenzyl)- | HCID 205282 | 84.5% |
反応手順
A suspension of 5-bromouracil (18.45 g, 96.6 mmol) in 300 mL of dichloroethane was treated with N,O-bis(trimethylsilyl)acetamide (48 mL, 39.5 g, 194 mmol). The reaction mixture was heated at 80° C. for 3 hr under the nitrogen. The solution was cooled down to ambient temperature, 2,6-difluorobenzyl bromide (25 g, 120 mmol) was added and the reaction mixture was heated at 80° C. overnight under the protection of nitrogen. The reaction was cooled down, quenched with MeOH (15 mL), and partitioned between dichloromethane (500 mL) and water (250 mL). The organic layer was washed with brine, dried (sodium sulfate), and evaporated to give a solid. The crude product was triturated with ether, filtered, and washed with ether three times to give compound 1 (15.2 g, 50%) as a white solid; MS (CI) m/z 316.90, 318.90 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06608197B2 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-a3597a87fcc54dd7aa65f2a5ad3fd52d |
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| 出典メモ | uspto-grants-2003_08 |
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