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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78298Generated: October 24, 2026

Methylamine → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/en/reaction/78298

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 147681497%

Reaction Steps

A suspension of methyl 4-chloropyridine-2-carboxylate HCl salt (89.0 g, 428 mmol) in MeOH (75 mL) at 0° C. was treated with a 2.0 M methylamine solution in THF (1 L) at a rate which kept the internal temp. below 5° C. The resulting mixture was stored at 3° C. for 5 h, then concentrated under reduced pressure. The resulting solids were suspended in EtOAc (1 L) and filtered. The filtrate was washed with a saturated NaCl solution (500 mL), dried (Na2SO4) and concentrated under reduced pressure to afford 4-chloro-N-methyl-2-pyridinecarboxamide as pale-yellow crystals (71.2 g, 97%): mp 41-43° C.; 1H-NMR (DMSO-d6) δ 2.81 (s, 3H), 7.74 (dd, J=5.1, 2.2 Hz, 1H), 8.00 (d, J=2.2, 1H), 8.61 (d, J=5.1 Hz, 1H), 8.85 (br d, 1H); CI-MS m/z 171 ((M+H)+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-8dcc56f8e6c04af3b8a4a71461d16393
Source noteuspto-grants-2014_09