Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69653Generated: October 25, 2026

Methyl 6-chloro-5-nitronicotinate → Ethyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylate

https://huagongshe.com/reaction/69653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-chloro-5-nitronicotinateHCID 346961—
ReactantEthyl thiomorpholine-3-carboxylateHCID 13604869—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylateHCID 5832444895%

Reaction Steps

Methyl 6-chloro-5-nitronicotinate (1.1 g, 5.10 mmol) was added to ethyl thiomorpholine-3-carboxylate (2.0 g, 11.41 mmol) neat while stirring at room temperature. The viscous yellow reaction was heated to 90° C. for one hour and then allowed to cool back to room temperature. The reaction was diluted with dichloromethane (20 mL) and purified via column chromatography (220 g SiO2, 20-30% gradient, ethyl acetate in hexanes) to yield the title compound (1.71 g, 95%) as a yellow oil. [M+H] calc'd for C15H18N2O6S, 356; found, 356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822470B2
Source datasetuspto-grants-2014_09
ORD IDord-2e44c9b0eb6d4d6dbf6b6b11b8f2d14e
Source noteuspto-grants-2014_09