Hydrogen Peroxide → HCID 20539972, compound
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][CH2:11][CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][CH:25]=1)[NH:22][C:21](=[O:26])[CH2:20][CH2:19]2)([OH:3])=[O:2].[OH:27]O>>[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([CH2:11][CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][CH:25]=1)[NH:22][C:21](=[O:26])[CH2:20][CH2:19]2)=[O:27])([OH:3])=[O:2]Participants
3
Procedure
Prepared analogous to Example 123 from 6-[4-(2-carboxyphenyl-mercapto)-butoxy]-3,4-dihydro-carbostyril and hydrogen peroxide. M.p.: 194°-196° C. Yield: 77.2% of theory.
Sources & evidence
- ORD record
- ord-95d9436f54bc43d99ee792a2c92bd7fb
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04329347
Reaction notes
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