1,3-Dichloro-2-isocyanatobenzene → HCID 57710276, compound
Reaction equation
[CH2:1]([N:3]([CH2:19][CH3:20])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11]2[CH:16]=[C:15]([NH:17][CH3:18])[N:14]=[CH:13][N:12]=2)=[CH:6][CH:5]=1)[CH3:2].[Cl:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([Cl:28])[C:23]=1[N:29]=[C:30]=[O:31]>>[Cl:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([Cl:28])[C:23]=1[NH:29][C:30](=[O:31])[N:17]([C:15]1[CH:16]=[C:11]([NH:10][C:7]2[CH:8]=[CH:9][C:4]([N:3]([CH2:1][CH3:2])[CH2:19][CH3:20])=[CH:5][CH:6]=2)[N:12]=[CH:13][N:14]=1)[CH3:18]Participants
3
Procedure
The title compound is prepared analogously as described in Example 105B from N-(4-diethylamino-phenyl)-N′-methyl-pyrimidine-4,6-diamine and 2,6-dichlorophenyl isocyanate.
Sources & evidence
- ORD record
- ord-a6804596c79f4f4dbc96d04c1e978b7a
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08552002B2
Reaction notes
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