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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447356Generated: October 31, 2026

Ethyl Acetate → Ro 14-7437

https://huagongshe.com/reaction/1447356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDimethylformamide diethylacetalHCID 70913—
Reactantethyl alpha-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetateHCID 70542724—
ProductRo 14-7437HCID 127597—

Reaction Steps

4.1 g of ethyl α-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 25 ml of ethyl acetate, treated with 3.1 ml (18.1 mmol) of N,N-dimethylformamide diethyl acetal and heated to boiling under reflux for 0.5 hour. After cooling, the separated material is filtered off under suction and recrystallised from ethanol. After chromatography of the mother liquor, there is obtained a second portion of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of the same purity; melting point 166°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316839
Source datasetuspto-grants-1982_02
ORD IDord-afca01ea50684e3eb1d5128c25e3dee2
Source noteuspto-grants-1982_02