3,4-Dimethoxyaniline → HCID 10253529, compound

HRID 639396Notes

Reaction equation

HRID 639396 reaction equation
Cl[C:2]1[N:7]=[C:6]([C:8]2[C:9]([C:14]3[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=3[Cl:21])=[N:10][N:11]([CH3:13])[CH:12]=2)[CH:5]=[CH:4][N:3]=1.[CH3:22][O:23][C:24]1[CH:25]=[C:26]([NH2:32])[CH:27]=[CH:28][C:29]=1[O:30][CH3:31]>>[Cl:21][C:15]1[CH:16]=[C:17]([Cl:20])[CH:18]=[CH:19][C:14]=1[C:9]1[C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:32][C:26]3[CH:27]=[CH:28][C:29]([O:30][CH3:31])=[C:24]([O:23][CH3:22])[CH:25]=3)[N:7]=2)=[CH:12][N:11]([CH3:13])[N:10]=1

Participants

3

Reactant 2

HCID 227703,4-DimethoxyanilineHCID 586416632-chloro-4-[3-(2,4-dichloro-phenyl)-1-methyl-1H-pyrazol-4-yl]-pyrimidine

Product 1

HCID 10253529HCID 10253529, compound

Procedure

The title compound is prepared as described in Example 1 but using 2-chloro-4-[3-(2,4-dichloro-phenyl)-1-methyl-1H-pyrazol-4-yl]-pyrimidine and 3,4-dimethoxy-phenylamine.

Sources & evidence

ORD record
ord-2cdbfc859ddb40de9fa35ed45f044448
Source dataset
uspto-grants-2010_04
Patent number
US07691855B2

Reaction notes

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