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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513898Generated: October 26, 2026

Methanol → [4-(2-Azepan-1-yl-ethoxy)-phenyl]-[6-methoxy-2-(2,4,6-trifluoro phenyl)-naphthalen-1-yl]-methanone

https://huagongshe.com/reaction/1513898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,4,6-Trifluorophenylboronic AcidHCID 2779329—
ReactantTrifluoromethanesulfonic acid 1-[4-(2-azepan-1-yl-ethoxy)-benzoyl]-6-methoxynaphthalen-2-yl esterHCID 57552509—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product[4-(2-Azepan-1-yl-ethoxy)-phenyl]-[6-methoxy-2-(2,4,6-trifluoro phenyl)-naphthalen-1-yl]-methanoneHCID 5755256335%

Reaction Conditions

Temperature100 °C

Reaction Steps

Dissolve trifluoromethanesulfonic acid 1-[4-(2-azepan-1-yl-ethoxy)-benzoyl]-6-methoxy-naphthalen-2-yl ester (990 mg, 1.8 mmol), 2,4,6-trifluorophenylboronic acid (634 mg, 3.6 mmol), potassium phosphate (2.2 g, 10.8 mmol), tetrakis(triphenylphosphine)palladium (416 mg, 0.4 mmol) in dry DMF (25 mL) and heat at 100° C. for 3 hours. Purify reaction by SCX column and by silica gel chromatography using a 1-3% gradient of methanol in dichloromethane to yield 320 mg (35%) of the title compound: mass spectrum (ion spray) m/z=534 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217032B2
Source datasetuspto-grants-2012_07
ORD IDord-ba70ba5e9e644db88e7cc7f59a1a67c6
Source noteuspto-grants-2012_07