HCID 10140053, compound → HCID 10791859, compound
Reaction equation
[Cl:1][C:2]1[C:3]([CH3:30])=[N:4][O:5][C:6]=1[NH:7][S:8]([C:11]1[CH:15]=[CH:14][S:13][C:12]=1[C:16]([NH:18][C:19]1[C:24]([CH3:25])=[CH:23][C:22]([CH3:26])=[C:21]([CH2:27][OH:28])[C:20]=1[CH3:29])=[O:17])(=[O:10])=[O:9].Cl[C:32]1C(C)=N[O:35][C:36]=1NS(C1C=CSC=1C(NC1C(C)=CC(C)=C(C(OC)=O)C=1C)=O)(=O)=O>>[Cl:1][C:2]1[C:3]([CH3:30])=[N:4][O:5][C:6]=1[NH:7][S:8]([C:11]1[CH:15]=[CH:14][S:13][C:12]=1[C:16]([NH:18][C:19]1[C:24]([CH3:25])=[CH:23][C:22]([CH3:26])=[C:21]([CH2:27][O:28][C:36](=[O:35])[CH3:32])[C:20]=1[CH3:29])=[O:17])(=[O:10])=[O:9]Participants
3
Procedure
N-(4-chloro-3-methyl-5-isoxazolyl)-2-(3-hydroxymethyl-2,4,6-trimethylphenylaminocarbonyl)thiophene-3-sulfonamide; and N-(4-chloro-3-methyl-5-isoxazolyl)-2-(3-methoxycarbonyl-2,4,6-trimethylphenylaminocarbonyl)thiophene-3-sulfonamide.
Sources & evidence
- ORD record
- ord-c872e66d993240cabed50c15e721a541
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331637B1
Reaction notes
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