6-(4-Isopropyl-piperazin-1-yl)-pyridin-3-yl-amine → [6-(4-Isopropylpiperazin-1-yl)pyridin-3-yl]-[5-(1H-pyrazol-4-yl)-imidazo[1,2-a]pyrazin-8-yl]amine
Reaction equation
COC1C=C(N[C:21]2[C:22]3[N:23]([CH:32]=[CH:33][N:34]=3)[C:24]([C:27]3[CH:28]=[N:29][NH:30][CH:31]=3)=[CH:25][N:26]=2)C=CC=1C(NCC1C=NC(C)=CC=1)=O.[CH:35]([N:38]1[CH2:43][CH2:42][N:41]([C:44]2[N:49]=[CH:48][C:47]([NH2:50])=[CH:46][CH:45]=2)[CH2:40][CH2:39]1)([CH3:37])[CH3:36]>>[CH:35]([N:38]1[CH2:39][CH2:40][N:41]([C:44]2[N:49]=[CH:48][C:47]([NH:50][C:21]3[C:22]4[N:23]([CH:32]=[CH:33][N:34]=4)[C:24]([C:27]4[CH:28]=[N:29][NH:30][CH:31]=4)=[CH:25][N:26]=3)=[CH:46][CH:45]=2)[CH2:42][CH2:43]1)([CH3:37])[CH3:36]Participants
3
Reactant 2
Product 1
Procedure
This compound may be prepared using the same methods as described for Compound 184, using 6(4-isopropylpiperazin-1-yl)pyridin-3-ylamine in Step 3. LCMS: Rt=0.72 min (95%), m/z (ESI) 404 (M+H)+.
Workup
- customThis compound may be prepared
Sources & evidence
- ORD record
- ord-2b02b2b4835948c78b644949c3312d7e
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893058B2
Reaction notes
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