(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(4-cyclopropylpiperazin-1-yl)-phenyl]amine → [4-(4-Cyclopropylpiperazin-1-yl)phenyl]-[5-(1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyrazin-8-yl]amine
Reaction equation
[CH:1]1([CH2:4][N:5]2[CH2:10][CH2:9][N:8]([C:11]3[CH:16]=[CH:15][C:14]([NH:17][C:18]4[C:19]5[N:20]([N:29]=[CH:30][N:31]=5)[C:21]([C:24]5[CH:25]=[N:26][NH:27][CH:28]=5)=[CH:22][N:23]=4)=[CH:13][CH:12]=3)[CH2:7][CH2:6]2)[CH2:3]C1.BrC1N2N=CN=C2C(NC2C=CC(N3CCN(C4CC4)CC3)=CC=2)=NC=1>>[CH:4]1([N:5]2[CH2:6][CH2:7][N:8]([C:11]3[CH:12]=[CH:13][C:14]([NH:17][C:18]4[C:19]5[N:20]([N:29]=[CH:30][N:31]=5)[C:21]([C:24]5[CH:25]=[N:26][NH:27][CH:28]=5)=[CH:22][N:23]=4)=[CH:15][CH:16]=3)[CH2:9][CH2:10]2)[CH2:1][CH2:3]1Participants
3
Reactant 2
Product 1
Procedure
This compound may be prepared using methods as described for Compound 46, using (5-bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(4-cyclopropylpiperazin-1-yl)-phenyl]amine. LCMS: Rt=0.84 (95%), m/z (ESI) 402 (M+H)+.
Workup
- customThis compound may be prepared
Sources & evidence
- ORD record
- ord-1efc6fe587264f8aaf7606db9287f461
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07501411B2
Reaction notes
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