2,3-Dichloro-5-(trifluoromethyl)pyridine → HCID 66837835, compound

HRID 73112Notes

Reaction equation

HRID 73112 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.[CH3:13][N:14]1[C:18]2[CH:19]=[CH:20][C:21]([CH2:23][NH:24][S:25]([C:28]3[CH:37]=[CH:36][C:31]([C:32]([O:34][CH3:35])=[O:33])=[CH:30][CH:29]=3)(=[O:27])=[O:26])=[CH:22][C:17]=2[N:16]=[N:15]1>>[Cl:8][C:7]1[C:2]([N:24]([CH2:23][C:21]2[CH:20]=[CH:19][C:18]3[N:14]([CH3:13])[N:15]=[N:16][C:17]=3[CH:22]=2)[S:25]([C:28]2[CH:29]=[CH:30][C:31]([C:32]([O:34][CH3:35])=[O:33])=[CH:36][CH:37]=2)(=[O:27])=[O:26])=[N:3][CH:4]=[C:5]([C:9]([F:12])([F:11])[F:10])[CH:6]=1

Participants

3

Reactant 2

HCID 1122342,3-Dichloro-5-(trifluoromethyl)pyridineHCID 66837875HCID 66837875, compound

Product 1

HCID 66837835HCID 66837835, compound

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-methyl-1H-benzo[d][1,2,3]triazol-5-yl)methyl)sulfamoyl)benzoate (step-1 of Example 30).

Sources & evidence

ORD record
ord-69dcdf1d992e4ac79a3e0e334207eeb6
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Reaction notes

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