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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292024Generated: November 2, 2026

Pyridine → HCID 13805986, compound

https://huagongshe.com/reaction/2292024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantHCID 13805968HCID 13805968—
SolventAcetonitrileHCID 6342—
ProductHCID 13805986HCID 13805986—

Reaction Conditions

Temperature0 °C

Reaction Steps

2,2,2-Trichloroethylchloroformate (1.0 ml) was added dropwise to a solution of 2-ethyl-5-methyl-2H-1,4-thiazin-3(4H)-one (0.94 g) and pyridine (0.96 ml) in acetonitrile (30 ml) under ice-cooling, and the mixture was stirred at 0° C. for 30 minutes. Then the mixture was further stirred at ambient temperature for 18 hours. The solvent was removed under reduced pressure and the residue was extracted with ethyl acetate, was washed with water, 2N hydrochloric acid and water in the order named, and was dried over magnesium sulfate. The solvent was removed under reduced pressure to give 2-ethyl-5-methyl-6-[1-(2,2,2-trichloroethoxycarbonyl)-1,4-dihydro-4-pyridinyl]-2H-1,4-thiazin-3(4H)-one (2.0 g) as pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04800201
Source datasetuspto-grants-1989_01
ORD IDord-293904201ac9459fb07316eaf6cbb1b3
Source noteuspto-grants-1989_01