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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285124Generated: November 1, 2026

Pyridine → HCID 13518417, compound

https://huagongshe.com/reaction/1285124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
Reactant5-Methyl-2h-1,4-thiazin-3(4h)-oneHCID 290017—
ProductHCID 13518417HCID 1351841731.5%

Reaction Steps

To a solution of 5-methyl-2H-1,4-thiazin-3(4H)-one (1.5 g) in dry pyridine (20 ml), 2,2,2-trichloroethyl chloroformate (2.8 g) was added dropwise under ice bath temperature. The reaction mixture was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure and the residue was extracted with chloroform. The extract was washed with 2N hydrochloric acid and water, and dried over anhydrous magnesium sulfate and chloroform was removed under reduced pressure. The residual oil was triturated with ether and recrystallized from ethanol using decolorizing chacoal to give 5-methyl-6-[1-(2,2,2-trichloroethoxycarbonyl)-1,4-dihydro-4-pyridinyl]-2H-1,4-thiazin-3(4H)-one (1.4 g, yield 31.5%) as light yellow scales.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565813
Source datasetuspto-grants-1986_01
ORD IDord-a613680879944d79b41486a3146b774b
Source noteuspto-grants-1986_01