Hydrochloric Acid → 3-(5-diethylaminomethyl-1,2,4-oxadiazol-3-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride

HRID 1378069Notes

Reaction equation

HRID 1378069 reaction equation
[CH2:1]([N:3]([CH2:6][C:7]1[O:11][N:10]=[C:9]([C:12]2[N:13]=[CH:14][N:15]3[C:21]4[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:20]=4[C:19](=[O:27])[N:18]([CH3:28])[CH2:17][C:16]=23)[N:8]=1)[CH2:4][CH3:5])[CH3:2].[ClH:29]>C(O)C>[ClH:29].[CH2:1]([N:3]([CH2:6][C:7]1[O:11][N:10]=[C:9]([C:12]2[N:13]=[CH:14][N:15]3[C:21]4[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:20]=4[C:19](=[O:27])[N:18]([CH3:28])[CH2:17][C:16]=23)[N:8]=1)[CH2:4][CH3:5])[CH3:2]

Participants

4

Procedure

1.30 g (0.0034 mol) of 3-(5-diethylaminomethyl-1,2,4-oxadiazol-3-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo [1,5-a]-[1,4]benzodiazepin-6-one in 20 ml of ethanol were treated with 0.79 ml (0.0037 mol) of 4.78N ethanolic hydrochloric acid. Crystals separated after the addition of 100 ml of ether. There were obtained 1.28 g (90%) of 3-(5-diethylaminomethyl-1,2,4-oxadiazol-3-yl)-8-fluoro-5-methyl-5,6- dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one hydrochloride as white crystals; m.p. 220°-223° (dec.).

Workup

  1. customCrystals separated
  2. additionafter the addition of 100 ml of ether

Sources & evidence

ORD record
ord-5cb6c9d5354a462db16e36fd3fdb210f
Source dataset
uspto-grants-1997_09
Patent number
US05665718

Reaction notes

Loading…