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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257538Generated: November 2, 2026

1,2-Dichloroethane → HCID 66896048, compound

https://huagongshe.com/reaction/1257538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
ReactantHOAtHCID 181649—
ReactantSodium BicarbonateHCID 516892—
Reactant(1R)-1-(5-fluoropyridin-2-yl)ethan-1-amine hydrochlorideHCID 66690953—
ReactantHCID 66895359HCID 66895359—
SolventDimethylformamideHCID 6228—
ProductHCID 66896048HCID 6689604894%

Reaction Steps

To a solution of 3-bromo-5-[(5S)-5-(2-pyridinyl)-4,5-dihydro-3-isoxazolyl]benzoic acid hydrochloride (0.476 g, 1.24 mmol) in N,N-dimethylformamide (6 mL) were added (1R)-1-(5-fluoropyridin-2-yl)ethanamine hydrochloride (0.330 g, 1.55 mmol), EDC (416 mg, 2.17 mmol), HOAT (0.051 g, 0.372 mmol) and triethylamine (0.865 mL, 6.20 mmol). The reaction mixture was stirred at ambient temperature for 18 h. Saturated aqueous sodium bicarbonate was added. The mixture was extracted with dichloromethane (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (50% hexanes/ethyl acetate→0% hexanes/ethyl acetate) gave the title compound (547 mg). MS 468.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-f06d4e334b2845758b451b38a9379bea
Source noteuspto-grants-2013_06