6-Amino-2,3-dimethylpyridine → 2-chloro-N-(5,6-dimethylpyridin-2-yl)pyridine-3-sulfonamide
Reaction equation
[Cl:1][C:2]1[C:7]([S:8](Cl)(=[O:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:12][C:13]1[CH:14]=[CH:15][C:16]([NH2:20])=[N:17][C:18]=1[CH3:19]>N1C=CC=CC=1>[Cl:1][C:2]1[C:7]([S:8]([NH:20][C:16]2[CH:15]=[CH:14][C:13]([CH3:12])=[C:18]([CH3:19])[N:17]=2)(=[O:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound (5.0 g, 16.8 mmol) was prepared from 2-chloropyridine-3-sulfonyl chloride (5.0 g, 23.7 mmol) and 5,6-dimethylpyridin-2-amine (2.4 g, 19.6 mmol) in pyridine (25 mL) at rt using the methods of (IntC1), step 1.
Sources & evidence
- ORD record
- ord-fbb73121577d4a2b909a4d4609d65a3d
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09249160B2
Reaction notes
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