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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274193Generated: October 31, 2026

Diisopropylethylamine → Ethyl 6-chloro-4-(methylamino)pyridine-3-carboxylate

https://huagongshe.com/reaction/2274193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4,6-dichloropyridine-3-carboxylateHCID 600045—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventAcetonitrileHCID 6342—
ProductEthyl 6-chloro-4-(methylamino)pyridine-3-carboxylateHCID 2062700196.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of ethyl 4,6-dichloronicotinate (5.0 g, 22.7 mmol) in acetonitrile (50 mL) was added methylamine hydrochloride salt (1.84 g, 27.2 mmol) and diisopropylethylamine (14.6 g, 113.6 mmol), and the reaction mixture was heated at 70° C. overnight. LCMS showed the reaction was completed. The reaction was cooled to RT, quenched with water (50 mL) and extracted with ethyl acetate (3×100 mL). The organic layers were separated, combined, washed with water (50 mL) and brine (100 mL), dried over sodium sulfate, filtered, and concentrated to afford the title compound (4.7 g, crude), which was directly used in the next step without further purification. MS (ES+) C9H11ClN2O2 requires: 214, 216. Found: 215, 217 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126951B2
Source datasetuspto-grants-2015_09
ORD IDord-317c93cd3c8946d59656469a5309482f
Source noteuspto-grants-2015_09