3-Fluoroaniline → N-cyclopentyl-4-[2-[(3-fluorophenyl)amino]-4-pyridinyl]-2-pyrimidinamine
Reaction equation
Cl[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([NH:14][CH:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[N:9]=2)[CH:5]=[CH:4][N:3]=1.[F:20][C:21]1[CH:22]=[C:23]([CH:25]=[CH:26][CH:27]=1)[NH2:24]>>[CH:15]1([NH:14][C:10]2[N:9]=[C:8]([C:6]3[CH:5]=[CH:4][N:3]=[C:2]([NH:24][C:23]4[CH:25]=[CH:26][CH:27]=[C:21]([F:20])[CH:22]=4)[CH:7]=3)[CH:13]=[CH:12][N:11]=2)[CH2:19][CH2:18][CH2:17][CH2:16]1Participants
3
Procedure
The title compound was prepared in the same fashion as described in Example 7, Step D using 4-(2-chloro-4-pyridinyl)-N-cyclopentyl-2-pyrimidinamine (i.e., the product of Step A) and 3-fluoroaniline.
Sources & evidence
- ORD record
- ord-c842e093bb89462ebad84b41a514101e
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08026359B2
Reaction notes
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