Carbamic acid, [3-(bromoacetyl)phenyl]-, ethyl ester → HCID 178419570, compound
Reaction equation
[Br:1][CH2:2][C:3]([C:5]1[CH:6]=[C:7]([NH:11][C:12](=[O:16])[O:13][CH2:14][CH3:15])[CH:8]=[CH:9][CH:10]=1)=O.[C:17]([NH:20][C:21]([NH2:23])=[S:22])(=[NH:19])[NH2:18]>C(O)C>[BrH:1].[NH:20]([C:21]1[S:22][CH:2]=[C:3]([C:5]2[CH:6]=[C:7]([NH:11][C:12](=[O:16])[O:13][CH2:14][CH3:15])[CH:8]=[CH:9][CH:10]=2)[N:23]=1)[C:17]([NH2:19])=[NH:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 17.17 gm of ethyl N-[3-(2-bromoacetyl)-phenyl]-carbamate, 7.1 gm of amidinothiourea and 45 ml of ethanol was refluxed for 4 hours and then cooled to room temperature. The precipitate formed thereby was filtered off and washed with cold ethanol, yielding 22 gm of the title compound, m.p. 240°-2° C.