Cyclohexanemethylamine → Methyl-phenyl-carbamic Acid 4-(cyclohexylmethyl-carbamoyl)-phenyl Ester
Reaction equation
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([CH2:34][NH2:35])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1>>[CH:28]1([CH2:34][NH:35][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])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1Participants
3
Procedure
The title product was prepared from 4-(methyl-phenyl-carbamoyloxy)-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester and C-cyclohexyl-methylamine. The crude product was used without further purification (84%, oil). HPLC-MS: m/z=367.3 (M+1); Rt: 4.28 min.
Workup
- customThe crude product was used without further purification (84%, oil)
Sources & evidence
- ORD record
- ord-659ca4e08dc5495b85c0c9238338adda
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067517B2
Reaction notes
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