Hydrogen Bromide → 6-Chloro-7-hydroxy-3,4-dihydrocarbostyril
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12]C)[NH:8][C:7](=[O:14])[CH2:6][CH2:5]2.Br>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[NH:8][C:7](=[O:14])[CH2:6][CH2:5]2Participants
3
Procedure
The thus-obtained 30 g of 6-chloro-7-methoxy-3,4-dihydrocarbostyril are dispersed in 300 ml of 47%-hydrobromic acid aqueous solution and heated for 4 hours under refluxing condition. After cooling of the reaction mixture, the insoluble matter is separated by filtration, washed with water and dried. Recrystallization from methanol-chloroform obtains 25 g of 6-chloro-7-hydroxy-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with a melting point of 264°-266° C.
Workup
- temperatureheated for 4 hours
- temperatureunder refluxing condition
- temperatureAfter cooling of the reaction mixture
- customthe insoluble matter is separated by filtration
- washwashed with water
- customdried
- customRecrystallization from methanol-chloroform
Sources & evidence
- ORD record
- ord-deebe12d0b1a4f63a72710d06dcbe783
- Source dataset
- uspto-grants-1989_04
- Patent number
- US04824840
Reaction notes
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