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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156236Generated: October 27, 2026

Bromazepam → 7-Bromo-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-ylidenepropanedioic acid diethyl ester

https://huagongshe.com/reaction/1156236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromazepamHCID 2441—
ReactantTetrahydrofuranHCID 8028—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantSodium hydrideHCID 24758—
Reactant2,2-DiethylpropanedioateHCID 6951563—
Product7-Bromo-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-ylidenepropanedioic acid diethyl esterHCID 70543778—

Reaction Steps

Diethylmalonate (45.55 ml) was added to THF (200 ml). The mixture was maintained at room temperature while sodium hydride (16 g of a 60% oil dispersion) was added over 1 hr. To the resulting suspension, diethyl chlorophosphate (14.45 ml) was added dropwise over 50 minutes. After a 30 minute agitation cycle, a THF solution of 7-bromo-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-one (15.8 g) was added dropwise over 20 minutes. The resulting solution was allowed to agitate for 1 hr. The pH was adjusted from 5.0 to 5.5, and the reaction solution was vacuum concentrated (40° C./30 mm) to remove the THF. To the residue was added cold water (600 ml) and hexane (100 ml). The crystalline solid obtained was filtered and washed with cold water and hexane. After the solid was dried to constant weight, the end product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335042
Source datasetuspto-grants-1982_06
ORD IDord-7a6e9d2072ba4ea5bc1c4efb374da6c0
Source noteuspto-grants-1982_06