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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762125Generated: November 4, 2026

Pyridine → N-(6-methoxypyridin-3-yl)cyclopropanecarboxamide

https://huagongshe.com/reaction/1762125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium HydroxideHCID 14798—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(6-methoxypyridin-3-yl)cyclopropanecarboxamideHCID 86308—

Reaction Steps

5-Amino-2-methoxy pryidine (12.4 g, 0.10 mol) and pyridine (10 ml) were mixed together in dichloromethane (200 ml) in a reaction flask. Cyclopropane carboxylic acid chloride (9.1 ml, 0.10 mol) was added to the reaction mixture over a period of 2 minutes. The reaction was exothermic and the temperature rose to 34° C. The reaction was allowed to stand for one hour at room temperature, after which the reaction mixture was wsahed with 5% sodium hydoxide (200 ml) and water (100 ml). The resulting organic phase was separated and dried over anhydrous magnesium sulfate. Crystals formed, so the mixture was filtered and washed with 300 ml of acetone and the filtrate evaporated in vacuo to give a solid that was triturated with hexane to yield 16.7 g, after drying. The product was identified by infrared (IR) and nuclear magnetic spectroscopy (NMR) analysis as the title compound, having a melting pont of 130°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831044
Source datasetuspto-grants-1989_05
ORD IDord-6fcbd6b82e15420aa6397bcffd67dc62
Source noteuspto-grants-1989_05