Ammonia → HCID 86649911, compound
Reaction equation
[NH3:1].[Cl:2][C:3]1[N:4]=[CH:5][N:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][C:11]([N:16]=[C:17]=[S:18])=[CH:10][C:9]=2[F:19])[CH:7]=1>>[Cl:2][C:3]1[N:4]=[CH:5][N:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][C:11]([NH:16][C:17]([NH2:1])=[S:18])=[CH:10][C:9]=2[F:19])[CH:7]=1Participants
3
Procedure
Step M (8): Methanolic ammonia (2.0 M, 5 mL, 10 mmol) was added to a flask charged with 4-chloro-1-(2-fluoro-4-isothiocyanato-6-methoxyphenyl)-1H-imidazole (230 mg, 0.811 mmol). After 2 h, the reaction mixture was concentrated in vacuo to afford 1-(4-(4-chloro-1H-imidazol-1-yl)-3-fluoro-5-methoxyphenyl)thiourea (244 mg, 100% yield). LC-MS (M+H)+ 301.1.
Workup
- concentrationthe reaction mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-7a7e8bfcb84243a9a79a324166dbf66a
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349880B2
Reaction notes
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