N-bromobutanimide → 4-(2',4'-Dichlorophenyl)-5-bromomethyl thiazole
反応式
Br.[Cl:2][C:3]1[CH:8]=[C:7]([Cl:9])[CH:6]=[CH:5][C:4]=1[C:10]1[N:11]=[CH:12][S:13][C:14]=1[CH3:15].[Br:16]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[Cl:2][C:3]1[CH:8]=[C:7]([Cl:9])[CH:6]=[CH:5][C:4]=1[C:10]1[N:11]=[CH:12][S:13][C:14]=1[CH2:15][Br:16]参加物
4
実験手順
The product was neutralised and the free thiazole was treated with N-bromosuccinimide in refluxing carbon tetrachloride for 16 hours with irradiation by a lamp to give 4-(2',4'-dichlorophenyl)-5-bromomethyl thiazole The crude product was dissolved in dry acetonitrile, sodium triazole (0.91 g; 0.01 mole) was added and the mixture stirred for 16 hours at 20° C. to give, after chromatography using silica gel/chloroform: 2% ethanol, the title compound (0.71 g; 23%). m.p. 120°-123° C.
後処理
- customwith irradiation by a lamp
出典と根拠
- ORDレコード
- ord-1e890ddce1dd460591518f7d5749c05a
- 出典データセット
- uspto-grants-1994_07
- 特許番号
- US05332753
反応ノート
読み込み中…