Cyclopropylamine → Methyl-phenyl-carbamic Acid 4-cyclopropylcarbamoyl-phenyl Ester
反応式
O=C1CCC(=O)N1O[C:9](=[O:27])[C:10]1[CH:15]=[CH:14][C:13]([O:16][C:17](=[O:26])[N:18]([CH3:25])[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:12][CH:11]=1.[CH:28]1([NH2:31])[CH2:30][CH2:29]1>>[CH:28]1([NH:31][C:9]([C:10]2[CH:11]=[CH:12][C:13]([O:16][C:17](=[O:26])[N:18]([CH3:25])[C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)=[CH:14][CH:15]=2)=[O:27])[CH2:30][CH2:29]1参加物
3
実験手順
The title product was prepared from 4-(methyl-phenyl-carbamoyloxy)-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester and cyclopropylamine. The crude product was used without further purification (97%, oil). HPLC-MS: m/z=311.2 (M+1); Rt: 3.21 min.
後処理
- customThe crude product was used without further purification (97%, oil)
出典と根拠
- ORDレコード
- ord-ffcb0d2fd58d41ed9006d5f5a977a37d
- 出典データセット
- uspto-grants-2006_06
- 特許番号
- US07067517B2
反応ノート
読み込み中…