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

HRID 13146Notes

Reaction equation

HRID 13146 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]=1

Participants

3

Procedure

Prepared as described for 118a using 1-(6-Chloro-pyridazin-3-yl)-5-iodo-1H-indazole (119b). Yield 35 mg (7%).

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-82dcc6b701f64901b11501d8515bb057
Source dataset
uspto-grants-2010_06
Patent number
US07728030B2

Reaction notes

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