Iodine → HCID 20374817, compound
Reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:10][C:11](=[S:22])[NH:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([S:20][CH3:21])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1.[O-][CH2:24][CH3:25].[Na+].II>C(O)C>[S:22]([C:11]1[NH:12][C:13]([C:25]2[CH:24]=[CH:18][C:17]([S:20][CH3:21])=[CH:16][CH:15]=2)=[C:9]([C:6]2[CH:5]=[CH:4][C:3]([S:2][CH3:1])=[CH:8][CH:7]=2)[N:10]=1)[C:11]1[NH:10][C:9]([C:6]2[CH:5]=[CH:4][C:3]([S:2][CH3:1])=[CH:8][CH:7]=2)=[C:13]([C:14]2[CH:19]=[CH:18][C:17]([S:20][CH3:21])=[CH:16][CH:15]=2)[N:12]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4,5-bis(4-methylthiophenyl)-1H-imidazole-2-thione (5.2 g, 0.015 mol), sodium ethoxide (1.0 g, 0.015 mol) and iodine (1.9 g, 0.0075 mol) in ethanol (70 ml) was stirred at ambient temperature for three hours. The resulting solid was collected, washed with ethanol and then ether. Recrystallization from N,N-dimethylformamide give the title compound, m.p. 297°-298°.
Workup
- customThe resulting solid was collected
- washwashed with ethanol
- customRecrystallization from N,N-dimethylformamide
Sources & evidence
- ORD record
- ord-cd09ca7b091442fca1e841e62ed2dee5
- Source dataset
- uspto-grants-1980_02
- Patent number
- US04188397
Reaction notes
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