2-chloro-N-(2-(isopropylsulfonyl)phenyl)-5-methylpyrimidin-4-amine → N2-[6-(dimethylphosphoryl)-2-methoxypyridin-3-yl]-5-methyl-N4-[2-(propan-2-ylsulfonyl)phenyl]pyrimidine-2,4-diamine

HRID 921343Notes

Reaction equation

HRID 921343 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([CH:18]([CH3:20])[CH3:19])(=[O:17])=[O:16])[C:5]([CH3:21])=[CH:4][N:3]=1.[CH3:22][P:23]([C:26]1[N:31]=[C:30]([O:32][CH3:33])[C:29]([NH2:34])=[CH:28][CH:27]=1)([CH3:25])=[O:24]>>[CH3:25][P:23]([C:26]1[N:31]=[C:30]([O:32][CH3:33])[C:29]([NH:34][C:2]2[N:7]=[C:6]([NH:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15]([CH:18]([CH3:20])[CH3:19])(=[O:17])=[O:16])[C:5]([CH3:21])=[CH:4][N:3]=2)=[CH:28][CH:27]=1)([CH3:22])=[O:24]

Participants

3

Procedure

This compound can be prepared as in Example 32 by reacting 2-Chloro-5-methyl-N-[2-(propan-2-ylsulfonyl)phenyl]-pyrimidin-4-amine with 6-(dimethylphosphoryl)-2-methoxypyridin-3-ylamine (prepared in Example 32).

Workup

  1. customThis compound can be prepared as in Example 32

Sources & evidence

ORD record
ord-7fa63ac278fe473194916d921169f1e5
Source dataset
uspto-grants-2016_03
Patent number
US09273077B2

Reaction notes

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