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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916882Generated: October 30, 2026

Potassium Carbonate → N-(1-Fluorobenzyl)-N-indan-2-yl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl]acetamide

https://huagongshe.com/reaction/916882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6,7-Dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 12627730—
ReactantN-(1-fluorobenzyl)-N-indan-2-yl-2-bromoacetamideHCID 69183190—
SolventAcetonitrileHCID 6342—
ProductN-(1-Fluorobenzyl)-N-indan-2-yl-2-(6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl]acetamideHCID 6949432778%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (160, 153 mg, 0.5 mmol), N-(1-fluorobenzyl)-N-indan-2-yl-2-bromoacetamide (161, 180 mg, 0.5 mmol) and potassium carbonate (500 mg) in acetonitrile is heated at 80° C. overnight. After cooling, the mixture is filtered and concentrated. The resulting residue is purified by column chromatography eluting with 5% methanol in chloroform to provide the title product (162) as a thick oil (215 mg, 78%). 1H NMR (CDCl3) 6.8–7.3 (m, 14H), 6.60(s, 1H), 6.05 (s, 1H),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271270B2
Source datasetuspto-grants-2007_09
ORD IDord-3aa6506ffe774da2a156d3c9687e50c1
Source noteuspto-grants-2007_09