Acetic Acid → HCID 20083120, compound
Reaction equation
[Cl:1][C:2]1[C:3]([F:21])=[C:4]2[C:9]3=[C:10]([C:12](=[O:19])[C:13]([C:15]([O:17]C)=[O:16])=[CH:14][N:8]3[N:7]([CH3:20])[CH2:6][CH2:5]2)[CH:11]=1.Cl.C(O)(=O)C>O>[Cl:1][C:2]1[C:3]([F:21])=[C:4]2[C:9]3=[C:10]([C:12](=[O:19])[C:13]([C:15]([OH:17])=[O:16])=[CH:14][N:8]3[N:7]([CH3:20])[CH2:6][CH2:5]2)[CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To 600 mg (1.9 mmol) of the compound (133) obtained in Example 25, 5 ml of concentrated hydrochloric acid and 20 ml of acetic acid were added, and the solution was heated at reflux for 2 hours. After air-cooling, 20 ml of water was added to the solution, and solids were filtered off and washed with ethanol and ether in this order to obtain 461 mg of the subject compound (134) in a 80% yield.
Workup
- temperaturethe solution was heated
- temperatureat reflux for 2 hours
- temperatureAfter air-cooling
- filtrationwere filtered off
- washwashed with ethanol and ether in this order
Sources & evidence
- ORD record
- ord-529dc38516d94057a188df75f8909de0
- Source dataset
- uspto-grants-1993_10
- Patent number
- US05254685
Reaction notes
Loading…