反応式
Cl.C(O[C:5](=[NH:16])[CH2:6][S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:9])=[O:8])C.[OH-].[Na+].[CH3:19][C:20]1[CH:21]=[C:22]([C:26]([NH:28][NH2:29])=[O:27])[O:23][C:24]=1[CH3:25]>C(Cl)(Cl)Cl>[NH2:16][C:5](=[N:29][NH:28][C:26]([C:22]1[O:23][C:24]([CH3:25])=[C:20]([CH3:19])[CH:21]=1)=[O:27])[CH2:6][S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:9])=[O:8]参加物
実験手順
A suspension of 1.18 g (0.004 mol) 2-(phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride in 15 ml chloroform was treated with 6 ml 1N aqueous sodium hydoxide. The mixture was extracted with dichloromethane. The extracts were combined and dried with magnesium sulfate and the solvents were distilled off under reduced pressure. The resulting colorless oil was stirred together with 0.68 g (0.004 mol) 4,5-dimethyl-furan-2-carboxylic acid hydrazide in 10 ml chloroform for 24 hours at reflux temperature. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 19/1 gave 1.14 g (76%) 4,5-dimethyl-furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide as white crystals with mp. 197-199° C., MS m/e (%): 336 (M+H+, 100).
後処理
- extractionThe mixture was extracted with dichloromethane
- dry with materialdried with magnesium sulfate
- distillationthe solvents were distilled off under reduced pressure
- temperatureat reflux temperature
- customEvaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 19/1
出典と根拠
- ORDレコード
- ord-6307b44407084017a86a0455aed26e3f
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06355653B1
関連ノート
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