HCID 57580664, compound → HCID 59022996, compound
Reaction equation
C(N1CCC(C2C=CC(N[C:17]3[C:18]4[N:19]([CH:33]=[CH:34][N:35]=4)[C:20]([C:23]4[CH:24]=[C:25]5[C:29](=[CH:30][CH:31]=4)[C:28](=[O:32])[NH:27][CH2:26]5)=[CH:21][N:22]=3)=CC=2)CC1)(C)C.[CH:36]([N:39]1[CH2:44][CH2:43][N:42]([C:45]2[CH:50]=[CH:49][C:48]([NH2:51])=[CH:47][C:46]=2[C:52]([F:55])([F:54])[F:53])[CH2:41][CH2:40]1)([CH3:38])[CH3:37]>>[CH:36]([N:39]1[CH2:40][CH2:41][N:42]([C:45]2[CH:50]=[CH:49][C:48]([NH:51][C:17]3[C:18]4[N:19]([CH:33]=[CH:34][N:35]=4)[C:20]([C:23]4[CH:24]=[C:25]5[C:29](=[CH:30][CH:31]=4)[C:28](=[O:32])[NH:27][CH2:26]5)=[CH:21][N:22]=3)=[CH:47][C:46]=2[C:52]([F:55])([F:54])[F:53])[CH2:43][CH2:44]1)([CH3:38])[CH3:37]Participants
3
Procedure
This compound may be prepared using the methods as described for Compound 206, using 4-(4-isopropylpiperazin-1-yl)-3-(trifluoromethyl)phenylamine in Step 3. LCMS: Rt=0.98 min (95%), m/z 536 (M+H)+.
Workup
- customThis compound may be prepared
Sources & evidence
- ORD record
- ord-47e6e705cf02446ea7fd790a120e1fc1
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178530B2
Reaction notes
Loading…