Benzoyl isothiocyanate → HCID 19089190, compound
Reaction equation
[C:1]([N:9]=[C:10]=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:12][C:13]1[C:18]([CH3:19])=[CH:17][CH:16]=[CH:15][C:14]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>ClCCl>[C:1]([NH:9][C:10]([NH:12][C:13]1[C:18]([CH3:19])=[CH:17][CH:16]=[CH:15][C:14]=1[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of benzoylisothiocyanate (8.78 g), 2-amino-3-methylbiphenyl (9.85 g) and dichloromethane (75 ml) at ambient temperature for two hours gave N-benzoyl-N'-(3-methyl-2-biphenylyl)thiourea (m.p. 172°-173° C.).
Sources & evidence
- ORD record
- ord-a7ec013a0d254b20a4b43d2a84504bff
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05302720
Reaction notes
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