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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860807Generated: October 31, 2026

2-Propanol, reaction products with ammonia, distn. residues → 2H-1,4-Benzodiazepin-2-one

https://huagongshe.com/reaction/860807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanol, reaction products with ammonia, distn. residuesHCID 18331942—
ReactantHCID 69020457HCID 69020457—
SolventTetrahydrofuranHCID 8028—
Product2H-1,4-Benzodiazepin-2-oneHCID 21864639151.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

NH3/2-propanol (40 ml) was added dropwise at 5° C. to a mixture of 7-[chloro(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-5-(3-chlorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one (described in Example B10a) (0.0075 mol) in THF (40 ml). The mixture was stirred at 5° C. for 30 min, hydrolyzed and extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness. The residue (4 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97.5/2.5/0.1 and 96/4/0.1; 15–40 μm). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from acetonitrile and diethyl ether. The precipitate was filtered off and dried, yielding 1.8 g (48%) of 2H-1,4-benzodiazepin-2-one, 7-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-5-(3-chlorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one, mp. 213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153958B2
Source datasetuspto-grants-2006_12
ORD IDord-bc24aaf550774d978b2902aca1f54434
Source noteuspto-grants-2006_12