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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706335Generated: October 30, 2026

Oxalyl chloride → 2-Methylpyridine-3-carbonyl chloride

https://huagongshe.com/reaction/706335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methylnicotinic acidHCID 643373—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Methylpyridine-3-carbonyl chlorideHCID 12902598—

Reaction Steps

To a suspension of methylnicotinic acid (500 mg, 3.6 mmol) in DCM (30 mL) is added oxalyl chloride (0.93 mL, 10.9 mmol) dropwise followed by DMF (1 drop). The reaction mixture is stirred at room temperature for 1 h and then concentrated in vacuo to give methylnicotinoyl chloride in a quantitative yield. A solution of I-83.1 (250 mg, 0.93 mmol) and methylnicotinoyl chloride (159.0 mg, 1.02 mmol) in DCM is stirred at room temperature for 1 h with the addition of more methylnicotinoyl chloride (28.9 mg, 0.19 mmol). The reaction mixture is then diluted with saturated aqueous NaHCO3 and the combined organics are dried over Na2SO4, The solvent is removed in vacuo to give I-110 (360 mg, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174980B2
Source datasetuspto-grants-2015_11
ORD IDord-c4f9b93c97774a58893ec34b132b60d2
Source noteuspto-grants-2015_11