Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407714Generated: October 30, 2026

Pyridine → 1083317-25-2

https://huagongshe.com/reaction/2407714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-BromopropanedialHCID 74945—
ReactantPyridine-2-carbothioamideHCID 1549499—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
Product1083317-25-2HCID 5340377238.7%

Reaction Steps

Pyridine-2-carbothioamide (4.5 g) was dissolved in tetrahydrofuran (40 mL). Pyridine (7.9 mL) was added and the reaction was heated to reflux. 2-Bromomalonaldehyde (7.2 g) was added in dimethylsulfoxide (15 mL) dropwise over 10 minutes and the reaction was heated for 3 hours. The reaction was concentrated in vacuo and partitioned between ethyl acetate and sodium hydrogen carbonate aqueous solution. The aqueous layer was back extracted and the combined organic phase was washed with brine and concentrated. The crude reaction was purified by silica gel column chromatography using an eluant of 2% to 4% acetone/dichloromethane to obtain the title compound (2.4 g) with the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809538B2
Source datasetuspto-grants-2014_08
ORD IDord-baf63f454415478da477e274c7e461bb
Source noteuspto-grants-2014_08