Ethanol → HCID 12421492, compound
Reaction equation
[C:1]([C:3]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]([CH2:14][CH3:15])[N:4]=1)#N.[OH-:16].[Na+].C(O)C.[OH2:21]>>[CH2:14]([N:5]1[C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[C:12](=[O:13])[C:3]([C:1]([OH:21])=[O:16])=[N:4]1)[CH3:15]Participants
5
Procedure
A solution of 25 g 3-cyano-1-ethyl-1,4-dihydro-4-oxocinnoline, 100 g sodium hydroxide, 400 ml ethanol and 100 ml water was stirred at 70° C. for 3 hr. After the removal of ethanol by evaporation, to the mixture was added conc. hydrochloric acid to precipitate crystalline materials. Precipitates were separated by filtration, washed with water, ethyl ether/ethanol and dried to yield 25.6 g of the desired compound. Mp.=206°-208° C.
Workup
- customAfter the removal of ethanol
- customby evaporation
- additionto the mixture was added conc. hydrochloric acid
- customto precipitate crystalline materials
- customPrecipitates
- customwere separated by filtration
- washwashed with water, ethyl ether/ethanol
- customdried
Sources & evidence
- ORD record
- ord-b5094620c36f419188ece0f0a92babe6
- Source dataset
- uspto-grants-1995_02
- Patent number
- US05391549
Reaction notes
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