Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292029Generated: November 1, 2026

HCID 13518417, compound → 2H-1,4-Thiazin-3(4H)-one, 5-methyl-6-(4-pyridinyl)-

https://huagongshe.com/reaction/2292029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13518417HCID 13518417—
ReactantChloroform methanolHCID 21584188—
CatalystZincHCID 23994—
SolventFormic AcidHCID 284—
Product2H-1,4-Thiazin-3(4H)-one, 5-methyl-6-(4-pyridinyl)-HCID 306253237.1%

Reaction Steps

Zinc powder (1.7 g) was added to a solution of 5-methyl-6-[1-(2,2,2-trichloroethoxycarbonyl)-1,4-dihydro-4-pyridinyl]-2H-1,4-thiazin-3(4H)-one (1g) in formic acid (14 ml) and the mixture was stirred at ambient temperature for 3 hours. The mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in water (30 ml), was adjusted to pH 7.0 by 1N aqueous sodium hydroxide, was extracted with chloroform and was dried over magnesium sulfate. Chloroform was removed and the residue was purified by the preparative thin layer chromatography [Merck TLC plate, silica gel 60F254 (supplied by Merck & Co. Inc., U.S.A.), 20×20 cm, thickness=1 mm, developing solvent; chloroform/methanol=20:1] to give the titled compound (0.2 g, yield 37.1%) as pale yellow plates. The physiocochemical properties were as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04800201
Source datasetuspto-grants-1989_01
ORD IDord-2fa0a3eeaf2d45cfb80677ca47177c8c
Source noteuspto-grants-1989_01