HCID 22672087, compound → HCID 23378633, compound
Reaction equation
[CH:1]([N:4]([S:16]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:18])=[O:17])[C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][C:6]=1[OH:15])([CH3:3])[CH3:2].O[CH2:26][C:27]1[CH:28]=[C:29]2[C:34](=[CH:35][CH:36]=1)[CH:33]=[C:32]([C:37]([O:39]CC)=[O:38])[CH:31]=[CH:30]2>>[CH:1]([N:4]([S:16]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:18])=[O:17])[C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:12])([F:14])[F:13])=[CH:7][C:6]=1[O:15][CH2:26][C:27]1[CH:28]=[C:29]2[C:34](=[CH:35][CH:36]=1)[CH:33]=[C:32]([C:37]([OH:39])=[O:38])[CH:31]=[CH:30]2)([CH3:3])[CH3:2]Participants
3
Procedure
By using 2-(N-isopropyl-phenylsulfonylamino)-5-trifluoromethylphenol (prepared in Reference Example 24.) and ethyl 6-hydroxymethyl-2-naphthate, the title compound having the following physical data was obtained by the same procedure as Reference Example 18(b)→Example 2.
Sources & evidence
- ORD record
- ord-7a68f6bf73a8444ebc688d4bb0dfcb3d
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06448290B1
Reaction notes
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