2,6-Dihydroxy-4-methylquinoline → 4-Methyl-6-(4-phenylsulfinyl-butoxy)-carbostyril
Reaction equation
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([OH:12])[CH:10]=2)[NH:5][C:4](=[O:13])[CH:3]=1.[C:14]1([S:20]([CH2:22][CH2:23][CH2:24][CH2:25]Br)=[O:21])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH2:25][CH2:24][CH2:23][CH2:22][S:20]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:21])[CH:10]=2)[NH:5][C:4](=[O:13])[CH:3]=1Participants
3
Procedure
Prepared analogous to Example 140 from 4-methyl-6-hydroxy-carbostyril (m.p. 326°-330° C.) and 4-phenylsulfinyl-butyl bromide.
Sources & evidence
- ORD record
- ord-36ce530a1ebf42fa93046a5abc1bf66d
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04329347
Reaction notes
Loading…