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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325310Generated: October 28, 2026

Pyridine → HCID 20464813, compound

https://huagongshe.com/reaction/325310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 13191334HCID 13191334—
SolventDichloromethaneHCID 6344—
ProductHCID 20464813HCID 20464813—

Reaction Conditions

Temperature25 °C

Reaction Steps

A 2.4 g (0.022 mol) sample of methoxyacetyl chloride was added dropwise to a solution of 5.5 g (0.022 mol) 3-(N-2-methylnaphth-1-ylamino)-gamma-butyrolactone and 1.7 g (0.022 mol) pyridine in 100 ml dichloromethane. The reaction mixture was stirred one hour at about 25° C. and then heated under reflux for 6 hours. After cooling overnight, the reaction mixture was washed successively with water, saturated sodium bicarbonate solution, water, dried over magnesium sulfate and evaporated under reduced pressure. The residue was chromatographed through a silica gel column. Elution with 25% acetone/75% petroleum ether gave 4.3 g of the product, m.p. 42°-46° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440780
Source datasetuspto-grants-1984_04
ORD IDord-4cddc57f3d344207be0156996710d2da
Source noteuspto-grants-1984_04