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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67565Generated: October 30, 2026

Ethyl Acetate → Ro 14-7437

https://huagongshe.com/reaction/67565

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 form 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 numberUS04346035
Source datasetuspto-grants-1982_08
ORD IDord-9e728c76ecb9459baac72d659a7147d3
Source noteuspto-grants-1982_08