Ethanol → HCID 12421492, compound

HRID 274851Notes

Reaction equation

HRID 274851 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

  1. customAfter the removal of ethanol
  2. customby evaporation
  3. additionto the mixture was added conc. hydrochloric acid
  4. customto precipitate crystalline materials
  5. customPrecipitates
  6. customwere separated by filtration
  7. washwashed with water, ethyl ether/ethanol
  8. customdried

Sources & evidence

ORD record
ord-b5094620c36f419188ece0f0a92babe6
Source dataset
uspto-grants-1995_02
Patent number
US05391549

Reaction notes

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