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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241430Generated: October 31, 2026

Isobutyryl chloride → Ethyl 2-(difluoromethyl)-5-(isobutyramidomethyl)nicotinate

https://huagongshe.com/reaction/241430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyryl chlorideHCID 62325—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 5-(aminomethyl)-2-(difluoromethyl)nicotinate hydrochlorideHCID 71059730—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(difluoromethyl)-5-(isobutyramidomethyl)nicotinateHCID 7105974473.6%

Reaction Steps

In a thermally controlled reactor stir a mixture of ethyl 5-(aminomethyl)-2-(difluoromethyl)pyridine-3-carboxylate hydrochloride (198 g, 742.4 mmol, 1.0 equiv), DCM (3040 mL), and DIPEA (520 mL, 2.98 mol, 4 equiv), then add a solution of isobutyryl chloride (95 mL, 903 mmol, 1.2 equiv) at such a rate so that the internal temperature is held between 18° C. and 22° C. Stir for 90 min. Extract the reaction mixture with NaHCO3 (sat., 1 L). Add water (1 L) and DCM (1 L), and filter the resulting suspension through diatomaceous earth. Combine all organic phases, and dry over MgSO4. Remove the solids by filtration, and concentrate the filtrate under reduced pressure. Purify the resulting material by slurrying with iso-hexane:Et2O [1:1, 1 L]. Collect the solids by filtration, wash with cold iso-hexanes (500 ml), and dry under vacuum at 50° C. to give the title compound as an off-white crystalline powder (164 g). MS (m/z) 301 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648200B2
Source datasetuspto-grants-2014_02
ORD IDord-4f8fb5fe7e6446c4ac83758fda5afa03
Source noteuspto-grants-2014_02