2,3-Dichloro-5-(trifluoromethyl)pyridine → Methyl 4-(N-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-N-((1-(2-hydroxy-2-methylpropyl)-1H-indazol-5-yl)methyl)sulfamoyl)benzoate

HRID 73098Notes

Reaction equation

HRID 73098 reaction equation
Cl[C:2]1[C:7]([Cl:8])=[CH:6][C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1.[OH:13][C:14]([CH3:41])([CH3:40])[CH2:15][N:16]1[C:24]2[C:19](=[CH:20][C:21]([CH2:25][NH:26][S:27]([C:30]3[CH:39]=[CH:38][C:33]([C:34]([O:36][CH3:37])=[O:35])=[CH:32][CH:31]=3)(=[O:29])=[O:28])=[CH:22][CH:23]=2)[CH:18]=[N:17]1>>[Cl:8][C:7]1[C:2]([N:26]([CH2:25][C:21]2[CH:20]=[C:19]3[C:24](=[CH:23][CH:22]=2)[N:16]([CH2:15][C:14]([OH:13])([CH3:40])[CH3:41])[N:17]=[CH:18]3)[S:27]([C:30]2[CH:31]=[CH:32][C:33]([C:34]([O:36][CH3:37])=[O:35])=[CH:38][CH:39]=2)(=[O:29])=[O:28])=[N:3][CH:4]=[C:5]([C:9]([F:12])([F:11])[F:10])[CH:6]=1

Participants

3

Procedure

The titled compound was prepared according to the procedure described in step-2 of Example 1 from 2,3-dichloro-5-(trifluoromethyl)pyridine and methyl 4-(N-((1-(2-hydroxy-2-methylpropyl)-1H-indazol-5-yl)methyl)sulfamoyl)benzoate (step-3 of Example 22).

Sources & evidence

ORD record
ord-1fe8104008174f2dbdbb63ac78d32cff
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Reaction notes

Loading…