4-(4-Pyridin-3-yl-pyrimidin-2-ylamino)-benzoic acid ethyl ester → 4-Methyl-3-(4-thiazol-2-yl-pyrimidin-2-ylamino)-benzoic acid
Reaction equation
C([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][C:8]([CH3:11])=[C:7]([NH:12][C:13]2[N:18]=[C:17]([C:19]3[S:20][CH:21]=[CH:22][N:23]=3)[CH:16]=[CH:15][N:14]=2)[CH:6]=1)C.C(OC(=O)C1C=CC(NC2N=C(C3C=NC=CC=3)C=CN=2)=CC=1)C>>[CH3:11][C:8]1[CH:9]=[CH:10][C:5]([C:4]([OH:24])=[O:3])=[CH:6][C:7]=1[NH:12][C:13]1[N:18]=[C:17]([C:19]2[S:20][CH:21]=[CH:22][N:23]=2)[CH:16]=[CH:15][N:14]=1Participants
3
Procedure
4-methyl-3-(4-thiazol-2-yl-pyrimidin-2-ylamino)-benzoic acid ethyl ester prepared in Preparation 10 was used instead of 4-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzoic acid ethyl ester according to the similar procedure to Preparation 19 to give the titled compound as yellow solid.
Sources & evidence
- ORD record
- ord-b2b992e896c44b4787143c64e46ecb7b
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07501424B2
Reaction notes
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