1-(6-Chloro-pyridazin-3-yl)-5-iodo-1H-indazole → 2-[1-(6-Chloro-pyridazin-3-yl)-1H-indazol-5-yloxy]-1-methyl-2-phenyl-ethylamine
Reaction equation
[CH3:1][CH:2]([NH2:26])[CH:3]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[O:4]C1C=C2C(=CC=1)N(C1C=CC=CN=1)N=C2.[Cl:27][C:28]1[N:33]=[N:32][C:31]([N:34]2[C:42]3[C:37](=[CH:38][C:39](I)=[CH:40][CH:41]=3)[CH:36]=[N:35]2)=[CH:30][CH:29]=1>>[Cl:27][C:28]1[N:33]=[N:32][C:31]([N:34]2[C:42]3[C:37](=[CH:38][C:39]([O:4][CH:3]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)[CH:2]([NH2:26])[CH3:1])=[CH:40][CH:41]=3)[CH:36]=[N:35]2)=[CH:30][CH:29]=1Participants
3
Procedure
Prepared as described for 118a using 1-(6-Chloro-pyridazin-3-yl)-5-iodo-1H-indazole (119b). Yield 35 mg (7%).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-4ff625f5d6aa4ebcb439b5747995bf2a
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143290B2
Reaction notes
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