2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- → Ethyl 2-chloro-5-{3-[2-(ethoxycarbonyl)-1-methylvinyl]ureido}-benzoate
Reaction equation
[Cl:1][C:2]1[CH:12]=[CH:11][C:10]([N:13]=[C:14]=[O:15])=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH2:16]/[C:17](/[CH3:24])=[CH:18]\[C:19]([O:21][CH2:22][CH3:23])=[O:20]>>[Cl:1][C:2]1[CH:12]=[CH:11][C:10]([NH:13][C:14]([NH:16][C:17]([CH3:24])=[CH:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[O:15])=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5]Participants
3
Procedure
using ethyl 2-chloro-5-isocyanatobenzoate and ethyl 3-aminocrotonate there is obtained ethyl 2-chloro-5-{3-[2-(ethoxycarbonyl)-1-methylvinyl]ureido}-benzoate,
Sources & evidence
- ORD record
- ord-c69966cbd3164e5ea3b1e78dfa80ef1a
- Source dataset
- uspto-grants-1988_05
- Patent number
- US04746352
Reaction notes
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