2-Amino-4,6-dimethylpyridine → 1-amino-N-(5-((4,6-dimethylpyridin-2-yl)carbamoyl)-2-methylphenyl)isoquinoline-5-carboxamide

HRID 1051263Notes

Reaction equation

HRID 1051263 reaction equation
C([NH:5][C:6]1[C:15]2[CH:14]=[CH:13][CH:12]=[C:11]([C:16]([NH:18][C:19]3[CH:24]=[C:23]([C:25](=[O:37])[NH:26][C:27]4[CH:32]=[CH:31][CH:30]=[C:29]([C:33](F)(F)F)[CH:28]=4)[CH:22]=[CH:21][C:20]=3[CH3:38])=[O:17])[C:10]=2[CH:9]=[CH:8][N:7]=1)(C)(C)C.[NH2:39]C1C=C(C)C=C(C)N=1>>[NH2:5][C:6]1[C:15]2[CH:14]=[CH:13][CH:12]=[C:11]([C:16]([NH:18][C:19]3[CH:24]=[C:23]([C:25](=[O:37])[NH:26][C:27]4[CH:28]=[C:29]([CH3:33])[CH:30]=[C:31]([CH3:32])[N:39]=4)[CH:22]=[CH:21][C:20]=3[CH3:38])=[O:17])[C:10]=2[CH:9]=[CH:8][N:7]=1

Participants

3

Reactant 2

HCID 215072-Amino-4,6-dimethylpyridineHCID 1180907961-(t-butylamino)-N-(2-methyl-5-((3-(trifluoromethyl)phenyl)carbamoyl)phenyl)isoquinoline-5-carboxamide

Product 1

HCID 1180908851-amino-N-(5-((4,6-dimethylpyridin-2-yl)carbamoyl)-2-methylphenyl)isoquinoline-5-carboxamideYield 8%

Procedure

The procedures of Steps (1), (2) and (3) of Example 2 and Step (4) of Example 1 were repeated step by step, except for using 2-amino-4,6-dimethylpyridine instead of aniline in Step (1) of Example 2 to obtain the title compound (2.8 mg, 8%).

Sources & evidence

ORD record
ord-5e7ce748b4d04a33953026f3b8238edd
Source dataset
uspto-grants-2016_07
Patent number
US09388165B2

Reaction notes

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