HCID 314266, compound → HCID 136146339, compound
Reaction equation
[OH:1][C:2]1[CH:21]=[C:20]([O:22][CH2:23][CH2:24][OH:25])[CH:19]=[CH:18][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:8][CH:7]=1)=[S:5].[C:26]([C:34]1[CH:44]=[CH:43][C:37]([O:38][CH2:39][C:40](O)=[O:41])=[CH:36][C:35]=1[OH:45])(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[C:26]([C:34]1[CH:44]=[CH:43][C:37]([O:38][CH2:39][C:40]([O:25][CH2:24][CH2:23][O:22][C:20]2[CH:19]=[CH:18][C:3]([C:4](=[S:5])[C:6]3[CH:11]=[CH:10][C:9]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)=[CH:8][CH:7]=3)=[C:2]([OH:1])[CH:21]=2)=[O:41])=[CH:36][C:35]=1[OH:45])(=[O:33])[C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1Participants
3
Procedure
Following the general procedure of Example 17, the title compound is prepared by reacting equimolar amounts of the alcohol compound of Example 7 and 4-benzoyl-3-hydroxy-phenoxyacetic acid.
Sources & evidence
- ORD record
- ord-e4563000b7624c0fa2b26df49c607717
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06576797B1
Reaction notes
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