Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735022Generated: November 2, 2026

Propargyl bromide → HCID 15380030, compound

https://huagongshe.com/reaction/1735022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantDihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-oneHCID 15380028—
SolventDimethylformamideHCID 6228—
ProductHCID 15380030HCID 1538003019.8%

Reaction Steps

A mixture prepared from 1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]-benzodiazepin-6-one (8.3 gm, 35 mmole) and sodium hydride (1.65 gm, 50% in oil, 1.0 eq) in dimethylformamide (DMF, 80 ml) was stirred at room temperature for 1.5 hours under N2. It was cooled to ~0° C. To this solution was charged propargyl bromide (16.5 gm, 80% in toluene, 3 eq) and the mixture was stirred for another 1.5 hours at 0° C. At the end of the reaction, the solution was poured into 10% NaOH (250 ml), and extracted with dichloromethane (DCM 1 l). The DCM solution was washed with NaOH (250 ml), water (2×300 ml) and brine (2×300 ml), then dried over MgSO4 and concentrated to an oil. Purification was accomplished by flash chromatography (SiO2 column, 200 gm, eluted with 1:1 hexane:DCM, 4 l). The material thus purified weighed 7.1 gm, (74%) as an oil. It turned to solid upon trituration with ether. A 3 gram portion of this material was recrystallized from ether (150 ml) to afford 1.9 gm of yellow crystals, m.p. 104°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536717
Source datasetuspto-grants-1996_07
ORD IDord-34f793892826478abcc8e2cac1d3d3d9
Source noteuspto-grants-1996_07