3-Chlorobenzenesulphonyl chloride → 3-Chloro-N-(5-chloro-3-methoxy-2-pyrazinyl)benzenesulphonamide
Reaction equation
[Cl:1][C:2]1[N:3]=[C:4]([O:9][CH3:10])[C:5]([NH2:8])=[N:6][CH:7]=1.[Cl:11][C:12]1[CH:13]=[C:14]([S:18](Cl)(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=1>>[Cl:11][C:12]1[CH:13]=[C:14]([S:18]([NH:8][C:5]2[C:4]([O:9][CH3:10])=[N:3][C:2]([Cl:1])=[CH:7][N:6]=2)(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
Prepared by the method of Example 1 (reaction performed at room temperature) using 5-chloro-3-methoxy-2-pyrazinamine (0.1 g) and 3-chlorobenzenesulphonyl chloride (0.13 g).
Workup
- customPrepared by the method of Example 1 (reaction performed at room temperature)
Sources & evidence
- ORD record
- ord-06287af46a1947d5ace9ef076e46a709
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662825B2
Reaction notes
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