Hydrochloric Acid → HCID 178515194, compound

HRID 1387674Notes

Reaction equation

HRID 1387674 reaction equation
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([N:11]2[C:23](=[O:24])[C:14]3=[CH:15][NH:16][C:17]4[C:22]([N:13]3[C:12]2=[O:25])=[CH:21][CH:20]=[CH:19][CH:18]=4)=[CH:7][CH:6]=1)(=O)C.Cl>C(O)C>[OH:4][C:5]1[CH:10]=[CH:9][C:8]([N:11]2[C:23](=[O:24])[C:14]3=[CH:15][NH:16][C:17]4[C:22]([N:13]3[C:12]2=[O:25])=[CH:21][CH:20]=[CH:19][CH:18]=4)=[CH:7][CH:6]=1

Participants

4

Procedure

2-(4-Acetoxyphenyl)-imidazo[1,5,a]quinoxaline-1,3(2H,5H)-dione (250 mg) was added to an ethanol solution (50 mL) saturated with HCl. The solution was stirred for 2 hours and the solvent was removed in vacuo to yield 2-(4-Hydroxyphenyl)-imidazo[1,5,a]quinoxaline-1,3(2H,5H)-dione (Compound 41). m.p. 318-322° C.

Workup

  1. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-f8321a5ab9914d2c9a45a94b35d9ace9
Source dataset
uspto-grants-2001_07
Patent number
US06268496B1

Reaction notes

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