Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993997Generated: November 1, 2026

Methylamine → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/reaction/1993997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantMethyl 4-chloropyridine-2-carboxylate--hydrogen chloride (1/1)HCID 16655470—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-N-methylpicolinamideHCID 147681480.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 17.8 g (0.103 mol, 1 eq) of 4-chloro-pyridine-2-carboxylic acid methyl ester hydrochloride in 15 mL of methanol was cooled to 0° C. and slowly treated with a 2.0 M solution of methylamine in tetrahydrofuran at a rate that kept internal temperature below 5° C. The reaction mixture was stirred at 0° C. for 2 hours, then slowly allowed to warm up to ambient temperature and stirred for 18 hours. Solvent was removed in vacuum, approx. 200 mL of ethyl acetate was added and the resulting suspension was filtered. The precipitate was washed with 100 mL of ethyl acetate. The combined ethyl acetate solutions were washed three times with 100 mL of brine and dried over sodium sulfate. Solvent was removed in vacuum to yield 14.16 g of the product as orange oil. Yield: 80.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-57595a4904df482bb5eba88460e009a0
Source noteuspto-grants-2010_01