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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177022Generated: October 25, 2026

Triethylamine → 2-[1-(2-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile

https://huagongshe.com/reaction/2177022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Iodobenzoyl chlorideHCID 69112—
Reactant2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochlorideHCID 66924378—
Product2-[1-(2-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrileHCID 6692435698%

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 2-iodobenzoyl chloride (200 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 2-[1-(2-iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile was obtained as a solid. (320 mg; 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067897B2
Source datasetuspto-grants-2015_06
ORD IDord-1d65f1e4f82944bd9981bb2140312dea
Source noteuspto-grants-2015_06