Formaldehyde → Chloromethyl 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoate
反応式
[NH2:1][S:2]([C:5]1[C:6]([Cl:21])=[CH:7][C:8]([NH:14][CH2:15][C:16]2[O:17][CH:18]=[CH:19][CH:20]=2)=[C:9]([CH:13]=1)[C:10](Cl)=[O:11])(=[O:4])=[O:3].C=[O:23].Cl[CH2:25][Cl:26]>>[NH2:1][S:2]([C:5]1[C:6]([Cl:21])=[CH:7][C:8]([NH:14][CH2:15][C:16]2[O:17][CH:18]=[CH:19][CH:20]=2)=[C:9]([CH:13]=1)[C:10]([O:23][CH2:25][Cl:26])=[O:11])(=[O:4])=[O:3]参加物
反応条件
- 温度
- 90 °C
実験手順
A mixture of 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chloride (13) (0.040 mole) and paraformaldehyde (0.040 mole) is heated in a sealed vessel at 90° C. for 3 hours. The reaction is cooled, and the solids dissolved in dichloromethane. The solution is washed with 5% aqueous sodium bicarbonate, with water, and then with a saturated sodium chloride solution. The organic layer is dried over sodium sulfate, filtered and concentrated in vacuo to give crude product, which may be purified by column chromatography on silica gel with hexanes/ethyl acetate as eluent. The fractions that contain pure product may be combined and spin evaporated in vacuo to give chloromethyl 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoate (15). See eg., Bodor, et al., J. Med. Chem., 23, 469 (1980), and Ulich, et al., J. Am. Chem. Soc., (1921) 43: 660.
後処理
- temperatureThe reaction is cooled
- washThe solution is washed with 5% aqueous sodium bicarbonate, with water
- dry with materialThe organic layer is dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give crude product, which
- custommay be purified by column chromatography on silica gel with hexanes/ethyl acetate as eluent
- customspin evaporated in vacuo
出典と根拠
- ORDレコード
- ord-4b96aa9a517449fc9a17a54d1f132b9d
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07763612B2
反応ノート
読み込み中…