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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192492Generated: November 1, 2026

Ethyl Acetate → 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanamine

https://huagongshe.com/reaction/1192492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylphosphineHCID 68983—
Reactant7-(1-Azidoethyl)-5-chloro-8-(2-fluorophenyl)quinolineHCID 86656174—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanamineHCID 67248648—

Reaction Steps

To a stirred solution of 7-(1-azidoethyl)-5-chloro-8-(2-fluorophenyl)quinoline (0.037 g, 0.11 mmol) in tetrahydrofuran (0.3 mL) and water (0.0813 mL) was added 1.00 M trimethylphosphine in tetrahydrofuran (0.135 mL, 0.135 mmol) at room temperature and the mixture was stirred at room temperature for 1 hour. To the mixture was added ethyl acetate and the mixture was extracted with 1 N HCl twice. The combined extracts were neutralized with solid sodium bicarbonate, and extracted with dichloromethane. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue showed two peaks by LCMS with the same desired mass and was used directly in the next step (28 mg, 82%). LCMS calculated for C17H15ClFN2(M+H)+: m/z=301.1; found: 301.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-4f026b5251ab443abf5a5c9c70983bcd
Source noteuspto-grants-2014_03