p-Aminophenylacetic acid ethyl ester → (4-{[2-(3,3-Dicyclohexyl-ureido)-thiazole-5-carbonyl]-amino}-phenyl)-acetic acid ethyl ester
Reaction equation
[CH:1]1([N:7]([CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[C:8](=[O:18])[NH:9][C:10]2[S:11][C:12]([C:15](O)=[O:16])=[CH:13][N:14]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:25]([O:27][C:28](=[O:37])[CH2:29][C:30]1[CH:35]=[CH:34][C:33]([NH2:36])=[CH:32][CH:31]=1)[CH3:26]>>[CH2:25]([O:27][C:28](=[O:37])[CH2:29][C:30]1[CH:31]=[CH:32][C:33]([NH:36][C:15]([C:12]2[S:11][C:10]([NH:9][C:8]([N:7]([CH:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)[CH:19]3[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]3)=[O:18])=[N:14][CH:13]=2)=[O:16])=[CH:34][CH:35]=1)[CH3:26]Participants
3
Procedure
Prepared as described in general procedure (K) using 2-(3,3-dicyclohexyl-ureido)-thiazole-5-carboxylic acid and 4-aminophenylacetic acid ethylester.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-cc7d29c5f9574427b76e95e285908681
- Source dataset
- uspto-grants-2014_10
- Patent number
- USRE045183E1
Reaction notes
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