5-Chlorothiophene-2-sulfonyl chloride → HCID 10193429, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:4]([NH2:11])=[N:5][C:6]([CH3:10])=[C:7]([CH3:9])[N:8]=1.[Cl:12][C:13]1[S:17][C:16]([S:18](Cl)(=[O:20])=[O:19])=[CH:15][CH:14]=1>>[Cl:12][C:13]1[S:17][C:16]([S:18]([NH:11][C:4]2[C:3]([O:2][CH3:1])=[N:8][C:7]([CH3:9])=[C:6]([CH3:10])[N:5]=2)(=[O:20])=[O:19])=[CH:15][CH:14]=1Participants
3
Procedure
Prepared by the method of Example 1 using 3-methoxy-5,6-dimethyl-2-pyrazinamine and 5-chloro-2-thienylsulphonyl chloride.
Sources & evidence
- ORD record
- ord-9c047c96e8454e6aa1d5930f7a127d47
- Source dataset
- uspto-grants-2008_08
- Patent number
- US07410972B2
Reaction notes
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