Acetic Acid → HCID 178515233, compound

HRID 258375Notes

Reaction equation

HRID 258375 reaction equation
[C:1]1([N:7]2[C:11](=[O:12])[C:10](=[CH:13][N:14]([CH3:16])C)[NH:9][C:8]2=[O:17])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C[C:19]([CH3:22])([O-])[CH3:20].[K+].[C:24](O)(=O)[CH3:25]>CN(C)C=O.O1CCCC1>[C:1]1([N:7]2[C:11](=[O:12])[C:10]3=[CH:13][NH:14][C:16]4[CH2:24][CH2:25][CH2:20][CH2:19][C:22]=4[N:9]3[C:8]2=[O:17])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Procedure

To a solution of 3-Phenyl-5-(dimethylaminomethylene)-imidazoline-2,4-dione (1.3 g) in dimethylformamide (20 mL) at 0° C. was added 1M potassium tert-butoxide (5 mL) in tetrahydrofuran. After 5 min 2-Chlorocycloxeanone (700 mg) was added and the mixture was stirred for 30 min. Acetic acid (1 mL) was added and the solvent was removed at reduced pressure. To the resulting residue was added ammonium acetate (10 gm) and acetic acid (25 ml) and the mixture was heated to reflux for 4 h. The solvent was removed at reduced pressure and water (50 mL) was added. The resulting solid was collected, washed with methanol and dried to yield 2-Phenyl-6,7,8,9-tetrahydroimidazo[1,5,a]quinoxaline-1,3(2H,5H)-dione (Compound 21) as an off white solid, m.p. 236°-240° C.

Workup

  1. customthe solvent was removed at reduced pressure
  2. additionTo the resulting residue was added ammonium acetate (10 gm) and acetic acid (25 ml)
  3. temperaturethe mixture was heated
  4. temperatureto reflux for 4 h
  5. customThe solvent was removed at reduced pressure and water (50 mL)
  6. additionwas added
  7. customThe resulting solid was collected
  8. washwashed with methanol
  9. customdried

Sources & evidence

ORD record
ord-1008579bb0b242399bc921277cb7211a
Source dataset
uspto-grants-1993_11
Patent number
US05266698

Reaction notes

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