反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([S:11](=[O:15])(=[O:14])[NH:12][CH3:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].Cl[C:17]1C=CC(S(O)=O)=[CH:22][C:18]=1C(O)=O.C1(CN)CC1>>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([S:11](=[O:15])(=[O:14])[NH:12][CH2:13][CH:22]2[CH2:18][CH2:17]2)=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]参加物
4
実験手順
The title compound was synthesised according to the procedure described for 2-Chloro-5-methylsulfamoyl-benzoic acid from 2-Chloro-5-sulfino-benzoic acid and cyclopropylmethylamine and obtained in 81% yield. MS (m/e): 288.0 (MH−, 100%).
後処理
- customobtained in 81% yield
出典と根拠
- ORDレコード
- ord-fc1203deeb0949a888ece709f3315086
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07427612B2
関連ノート
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