Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710865Generated: November 1, 2026

Diethyl Pyrocarbonate → 2-chloro-N-methoxy-N,6-dimethylpyridine-3-carboxyamide

https://huagongshe.com/reaction/1710865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-6-methylnicotinic acidHCID 121724—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-chloro-N-methoxy-N,6-dimethylpyridine-3-carboxyamideHCID 131728320—

Reaction Steps

A solution of 2-chloro-6-methylnicotinic acid (1.00 g, 5.83 mmol) in tetrahydrofuran (10 mL) was successively added with N,O-dimethylhydroxyamine hydrochloride (910 mg, 9.33 mmol), N,N-diisopropylethylamine (3.00 g, 23.2 mmol) and DEPC (1.43 g, 8.77 mmol) on an ice bath, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 2-chloro-N-methoxy-N,6-dimethylpyridine-3-carboxyamide as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-6913e4a125714660b61a17f522a50a41
Source noteuspto-grants-2010_09