Benzoic acid, 2-isothiocyanato-, methyl ester → 3-(3-imidazol-1-ylpropyl)-2-sulfanylidene-1H-quinazolin-4-one
Reaction equation
[N:1]([C:4]1[CH:13]=[CH:12][CH:11]=[CH:10][C:5]=1[C:6]([O:8]C)=O)=[C:2]=[S:3].C[C:15]1[N:16]=[CH:17][N:18]([CH2:20][CH2:21][CH2:22][NH2:23])[CH:19]=1>>[N:18]1([CH2:20][CH2:21][CH2:22][N:23]2[C:6](=[O:8])[C:5]3[C:4](=[CH:13][CH:12]=[CH:11][CH:10]=3)[NH:1][C:2]2=[S:3])[CH:19]=[CH:15][N:16]=[CH:17]1Participants
3
Procedure
The compound was synthesized starting from methyl 2-isothiocyanatobenzoate (0.773 g, 4.0 mmol) and 3-(1H-imidazol-1-yl)propan-1-amine (9) (0.5 g, 4.0 mmol) as described above.
Workup
- customThe compound was synthesized
Sources & evidence
- ORD record
- ord-3211e807743642caa817a3800798cc5d
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09034907B2
Reaction notes
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