2-Benzoyl-4-chlorobenzoic acid → HCID 69156083, compound
Reaction equation
Cl.[OH:2][CH:3]([CH2:17][CH3:18])[CH2:4][NH:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([S:13]([NH2:16])(=[O:15])=[O:14])=[CH:9][CH:8]=1.[C:19]([C:27]1[CH:35]=[C:34]([Cl:36])[CH:33]=[CH:32][C:28]=1[C:29](O)=[O:30])(=O)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[Cl:36][C:34]1[CH:35]=[C:27]2[C:28](=[CH:32][CH:33]=1)[C:29](=[O:30])[N:5]([CH2:6][C:7]1[CH:8]=[CH:9][C:10]([S:13]([NH2:16])(=[O:14])=[O:15])=[CH:11][CH:12]=1)[C:4]([C:3](=[O:2])[CH2:17][CH3:18])=[C:19]2[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1Participants
3
Procedure
In the same manner as in Example 452, Step 2, the title compound was synthesized from 4-[(2-hydroxybutylamino)methyl]benzenesulfonamide hydrochloride and 2-benzoyl-4-chlorobenzoic acid.
Sources & evidence
- ORD record
- ord-01049d88d14d48a59a2e734ab56f3335
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07402595B2
Reaction notes
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