Hydrogen Peroxide → HCID 20540099, compound
Reaction equation
BrCCCC[O:6]C1C=C2C(=CC=1)NC(=O)CC2.SC1C=CN=CC=1.[N:25]1[CH:30]=[CH:29][C:28]([S:31][CH2:32][CH2:33][CH2:34][CH2:35][O:36][C:37]2[CH:38]=[C:39]3[C:44](=[CH:45][CH:46]=2)[NH:43][C:42](=[O:47])[CH2:41][CH2:40]3)=[CH:27][CH:26]=1.OO>>[N:25]1[CH:30]=[CH:29][C:28]([S:31]([CH2:32][CH2:33][CH2:34][CH2:35][O:36][C:37]2[CH:38]=[C:39]3[C:44](=[CH:45][CH:46]=2)[NH:43][C:42](=[O:47])[CH2:41][CH2:40]3)=[O:6])=[CH:27][CH:26]=1Participants
5
Procedure
Prepared analogous to Example 122 from 6-(4-bromo-butoxy)-3,4-dihydro-carbostyril and 4-mercapto-pyridine and subsequent oxidation of the intermediate 6-[4-(4-pyridyl-mercapto)-butoxy]-3,4-dihydro-carbostyril (m.p. 128°-133° C.) with hydrogen peroxide analogous to Example 123.
Sources & evidence
- ORD record
- ord-d3be88a7d1f64ca9892fa470d263cb61
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04329347
Reaction notes
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