Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646215Generated: November 1, 2026

Benzyl Bromide → HCID 10426535, compound

https://huagongshe.com/reaction/1646215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10421619HCID 10421619—
SolventDimethylformamideHCID 6228—
ProductHCID 10426535HCID 10426535—

Reaction Steps

To a solution of 11-amino-4,5-dihydro-1H-pyrazolo[3,4-a]acridine (2.36 g) in dry DMF (90 ml) was added NaH (60%)(0.50 g) slowly. The reaction was stirred at room temperature for 15 minutes and then benzyl bromide (1.88 g) was added and the reaction was stirred an additional 15 minutes. At the end of this time the product was precipitated with water, filtered off, washed well with water, and air dried to yield a product which was further purified by flash chromatography (5% Et3N-EtOAc). The product-containing fractions were combined, concentrated, and recrystallized from EtOAc to give 2.35 g, mp 206°-207°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05179100
Source datasetuspto-grants-1993_01
ORD IDord-93f7926f45384f12a64009d6c10eb067
Source noteuspto-grants-1993_01