Cyanamide → HCID 178499910, compound
Reaction equation
[ClH:1].[NH2:2][C:3]1[CH:4]=[C:5]([N:9]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])=[CH:16][CH:15]=3)[C:10]2=[O:26])[CH:6]=[CH:7][CH:8]=1.[N:27]#[C:28][NH2:29]>O1CCOCC1>[ClH:1].[NH:2]([C:3]1[CH:4]=[C:5]([N:9]2[CH2:13][CH2:12][N:11]([C:14]3[CH:15]=[CH:16][C:17]([CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])=[CH:18][CH:19]=3)[C:10]2=[O:26])[CH:6]=[CH:7][CH:8]=1)[C:28]([NH2:29])=[NH:27]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 1-(3-amino-phenyl)-3-[4-(2-methoxycarbonyl-ethyl)-phenyl] -imidazolidin-2-one hydrochloride by refluxing for three hours with cyanamide in dioxane.
Sources & evidence
- ORD record
- ord-8c7dbe2883e64b36b5a654ec196735aa
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05276049
Reaction notes
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