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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170073Generated: October 30, 2026

Water → (2-Methoxy-benzyl)-(5-phenyl-quinolin-2-yl)-amine

https://huagongshe.com/reaction/1170073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantPhenylboronic AcidHCID 66827—
Reactant(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amineHCID 67334552—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
Product(2-Methoxy-benzyl)-(5-phenyl-quinolin-2-yl)-amineHCID 68433822—

Reaction Steps

(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amine (200 mg, 0.583 mmol) was dissolved in 8 mL 1,2-dimethoxyethane and 4 mL 1M sodium carbonate solution. The reaction mixture was evacuated and backfilled with argon for three times to remove oxygen. Phenylboronic acid (88 mg, 0.699 mmol), palladium(II)acetate (7 mg, 0.029 mmol) and triphenylphosphine (16 mg, 0.058 mmol) were added. The reaction mixture was refluxed overnight. The reaction mixture was poured into 100 mL water and extracted three times with ethyl acetate (100 mL each). The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The residue purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100:0->80:20 gradient). The title compound was obtained as a white solid (191 mg, 96%), MS: m/e=341.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825253B2
Source datasetuspto-grants-2010_11
ORD IDord-21d65a832b624175ad5713536a122c5a
Source noteuspto-grants-2010_11