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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381901Generated: October 31, 2026

Thiazole → 2,2-dimethoxy-5-methyl-6-(3-ethoxycarbonyl-2,3-dihydro-2-thiazolyl)-2H-1,4-thiazin

https://huagongshe.com/reaction/1381901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
ReactantEthyl chloroformateHCID 10928—
Reactant2,2-dimethoxy-5-methyl-4H-1,4-thiazin-3-oneHCID 14369799—
SolventDichloromethaneHCID 6344—
Product2,2-dimethoxy-5-methyl-6-(3-ethoxycarbonyl-2,3-dihydro-2-thiazolyl)-2H-1,4-thiazinHCID 8674274419%

Reaction Steps

Ethyl chloroformate (1.0 g) was added dropwise to a stirred solution of thiazole (0.79 g) in dichloromethane (10 ml) under ice-cooling and the mixture was stirred at room temperature for 0.5 hour. Then, 2,2-dimethoxy-5-methyl-2H-1,4-thiazin-3(4H)-one (1.47 g) was added, and the mixture was stirred at room temperature for 3 hours. The solution was washed with saturated sodium bicarbonate aqueous solution, dried over magnesium sulfate and evaporated to dryness. The residue was chromatographed on silica gel (Merck Lobar column size B: Art.10401, solvent: ethyl acetate-n-hexane=2:3) to give 2,2-dimethoxy-5-methyl-6-(3-ethoxycarbonyl-2,3-dihydro-2-thiazolyl)-2H-1,4-thiazin-(4H-one (510 mg, yield 19%) as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804668
Source datasetuspto-grants-1989_02
ORD IDord-340368a6d3b84bbea1772620aeb1dd0c
Source noteuspto-grants-1989_02