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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364440Generated: October 25, 2026

Triethylamine → HCID 66924380, compound

https://huagongshe.com/reaction/1364440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
Reactant2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochlorideHCID 66924378—
ProductHCID 66924380HCID 6692438077%

Reaction Steps

A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (200 mg; 0.7 mmol) (Example 123, Step 3) was stirred at room temperature with 3-chlorobenzoyl chloride (129 mg; 0.7 mmol) and triethylamine (0.3 mL; 2.1 mmol) for 16 hours. Reaction was cooled and quenched with dilute HCl and mixture extracted with ethyl acetate (2×20 mL). Combined organics washed with water, saturated sodium bicarbonate, brine and dried over Na2SO4. Crude material was purified by chromatography using 0.5-2% methanol/DCM gradient to afford 2-[1-(3-chloro-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile as a white solid. (200 mg; 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888366B2
Source datasetuspto-grants-2011_02
ORD IDord-0549120ff35a4e28a8548774f15060bb
Source noteuspto-grants-2011_02