4-[(4,6-dimethylpyrimidin-2-yl)amino]benzoic acid → HCID 59401791, compound

HRID 1916931Notes

Reaction equation

HRID 1916931 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N:8]2[CH2:12][CH2:11][CH:10]([N:13]3[CH2:17][CH2:16][CH2:15][CH:14]3[CH3:18])[CH2:9]2)[CH:5]=[CH:4][C:3]=1[NH2:19].[CH3:20][C:21]1[CH:26]=[C:25]([CH3:27])[N:24]=[C:23]([NH:28][C:29]2[CH:37]=[CH:36][C:32]([C:33](O)=[O:34])=[CH:31][CH:30]=2)[N:22]=1>>[CH3:20][C:21]1[CH:26]=[C:25]([CH3:27])[N:24]=[C:23]([NH:28][C:29]2[CH:37]=[CH:36][C:32]([C:33]([NH:19][C:3]3[CH:4]=[CH:5][C:6]([N:8]4[CH2:12][CH2:11][CH:10]([N:13]5[CH2:17][CH2:16][CH2:15][CH:14]5[CH3:18])[CH2:9]4)=[CH:7][C:2]=3[CH3:1])=[O:34])=[CH:31][CH:30]=2)[N:22]=1

Participants

3

Procedure

The title compound was prepared in a manner substantially the same as example 1 by coupling 2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenylamine with 4-(4,6-dimethyl-pyrimidin-2-ylamino)benzoic acid. MS: 485.3 (M+H).

Sources & evidence

ORD record
ord-5383203da0fb4812ba2bb0b09279b0f3
Source dataset
uspto-grants-2013_12
Patent number
US08618159B2

Reaction notes

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