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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195751Generated: November 2, 2026

Velnacrine → 1-(2-Bromoethoxy)-1,2,3,4-tetrahydroacridin-9-amine

https://huagongshe.com/reaction/1195751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVelnacrineHCID 3655—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-BromoethanolHCID 10898—
ReactantSodium HydroxideHCID 14798—
Product1-(2-Bromoethoxy)-1,2,3,4-tetrahydroacridin-9-amineHCID 5453703167%

Reaction Steps

To a suspension of 9-amino-1,2,3,4-tetrahydroacridin-1-ol (7.55 g) in 40 ml of 2-bromoethanol was added 9.9 ml of trifluoroacetic acid. The reaction mixture was stirred at ambient temperature for 18 hrs, added to iced sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The combined organic extracts were washed with water, saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and evaporated. The residue was purified by flash chromatography (ethyl acetate →2% triethylamine/ethyl acetate) to give 7.6 g (67%) of a product. Recrystallization from methanol/water gave the analytical sample, mp 163.5°-164.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112829
Source datasetuspto-grants-1992_05
ORD IDord-90cd270a579a401686bfa62b31322479
Source noteuspto-grants-1992_05