Benzoyl chloride, 3-(chlorosulfonyl)- → HCID 86649794, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:4][N:3]=1.[Cl:12][S:13]([C:16]1[CH:17]=[C:18]([CH:22]=[CH:23][CH:24]=1)[C:19](Cl)=[O:20])(=[O:15])=[O:14]>>[CH:9]([O:8][C:5]1[CH:6]=[CH:7][C:2]([N:1]([C:19]([C:18]2[CH:17]=[C:16]([S:13]([Cl:12])(=[O:15])=[O:14])[CH:24]=[CH:23][CH:22]=2)=[O:20])[C:19]([C:18]2[CH:17]=[C:16]([S:13]([Cl:12])(=[O:15])=[O:14])[CH:24]=[CH:23][CH:22]=2)=[O:20])=[N:3][CH:4]=1)([CH3:11])[CH3:10]Participants
3
Procedure
The entitled compound was produced according to the method of Reference Example 5 but using 2-amino-5-isopropoxypyridine and 3-(chlorosulfonyl)benzoyl chloride as the starting materials.
Workup
- customThe entitled compound was produced
Sources & evidence
- ORD record
- ord-13297d7892ca4c0599674d9822324df9
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08420823B2
Reaction notes
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