N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide → 3-Azido-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-5-fluoro-4-methyl-benzamide
Reaction equation
[N:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([F:14])[C:12]=1[CH3:13])[C:7]([OH:9])=O)=[N+:2]=[N-:3].[NH2:15][C:16]1[C:17]([O:31][CH3:32])=[C:18]([NH:26][S:27]([CH3:30])(=[O:29])=[O:28])[CH:19]=[C:20]([C:22]([CH3:25])([CH3:24])[CH3:23])[CH:21]=1.N(C1C=C(C=CC=1C)C(NC1C=C(C(C)(C)C)C=C(NS(C)(=O)=O)C=1OC)=O)=[N+]=[N-]>>[N:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([F:14])[C:12]=1[CH3:13])[C:7]([NH:15][C:16]1[CH:21]=[C:20]([C:22]([CH3:24])([CH3:25])[CH3:23])[CH:19]=[C:18]([NH:26][S:27]([CH3:30])(=[O:29])=[O:28])[C:17]=1[O:31][CH3:32])=[O:9])=[N+:2]=[N-:3]Participants
4
Reactant 3
Product 1
Procedure
3-Azido-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-5-fluoro-4-methyl-benzamide was prepared from 3-azido-5-fluoro-4-methyl benzoic acid (U.S. Ser. No. 04/102,492) and N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methane-sulfonamide in the same manner as 3-azido-N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-benzamide (Example 15).
Sources & evidence
- ORD record
- ord-0653e04712fb4f4e9b73142020deed29
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214802B2
Reaction notes
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