4,5-Dimethoxy-2-methylaniline → N2-(4,5-Dimethoxy-2-methylphenyl)-N4-(5-adamantylisoxazol-3-yl)-2,4-pyrimidinediamine

HRID 1241602Notes

Reaction equation

HRID 1241602 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:13]=[C:12]([C:14]34[CH2:23][CH:18]5[CH2:19][CH:20]([CH2:22][CH:16]([CH2:17]5)[CH2:15]3)[CH2:21]4)[O:11][N:10]=2)[CH:5]=[CH:4][N:3]=1.[CH3:24][C:25]1[CH:31]=[C:30]([O:32][CH3:33])[C:29]([O:34][CH3:35])=[CH:28][C:26]=1[NH2:27]>>[CH3:33][O:32][C:30]1[C:29]([O:34][CH3:35])=[CH:28][C:26]([NH:27][C:2]2[N:7]=[C:6]([NH:8][C:9]3[CH:13]=[C:12]([C:14]45[CH2:23][CH:18]6[CH2:19][CH:20]([CH2:22][CH:16]([CH2:17]6)[CH2:15]4)[CH2:21]5)[O:11][N:10]=3)[CH:5]=[CH:4][N:3]=2)=[C:25]([CH3:24])[CH:31]=1

Participants

3

Reactant 2

HCID 2665854,5-Dimethoxy-2-methylanilineHCID 865886072-chloro-N4-(5-adamantylisoxazol-3-yl)-4-pyrimidineamine

Product 1

HCID 21060793N2-(4,5-Dimethoxy-2-methylphenyl)-N4-(5-adamantylisoxazol-3-yl)-2,4-pyrimidinediamine

Procedure

The title compound was prepared by the method described in Example 1 using 2-chloro-N4-(5-adamantylisoxazol-3-yl)-4-pyrimidineamine and 2-methyl-4,5-dimethoxyaniline. MS (MH+)=462.2; Calc'd for C26H31N5O3— 461.57.

Sources & evidence

ORD record
ord-4de9f1c2e65f4177b300e9163e326fbd
Source dataset
uspto-grants-2006_10
Patent number
US07115617B2

Reaction notes

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