1,3-Dichloro-2-isocyanatobenzene → HCID 57710227, compound
Reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([NH:9][C:10]2[CH:15]=[C:14]([NH2:16])[N:13]=[CH:12][N:11]=2)=[CH:5][CH:4]=1.[Cl:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([Cl:24])[C:19]=1[N:25]=[C:26]=[O:27]>>[Cl:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([Cl:24])[C:19]=1[NH:25][C:26]([NH:16][C:14]1[CH:15]=[C:10]([NH:9][C:6]2[CH:7]=[N:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[N:11]=[CH:12][N:13]=1)=[O:27]Participants
3
Procedure
The title compound is prepared analogously as described in Example 105B from N-(6-methoxy-pyridin-3-yl)-pyrimidine-4,6-diamine and 2,6-dichlorophenyl isocyanate.
Sources & evidence
- ORD record
- ord-f87c90ad0e74415eaa3fc20e148a0c2d
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08552002B2
Reaction notes
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