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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415061Generated: October 25, 2026

Dichloromethane → 2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazine

https://huagongshe.com/reaction/2415061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantO-ethyl chloromethanethioateHCID 5325481—
Reactant2-(2-Methoxyphenethyl)imino-5,5-dimethyl-1,3-thiazineHCID 22639987—
SolventWaterHCID 962—
Product2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazineHCID 2263998260%

Reaction Steps

To a mixture of 2-(2-methoxyphenethyl)imino-5,5-dimethyl-1,3-thiazine (0.28 g), triethylamine (0.15 g) and dichloromethane (5 ml) was added dropwise for 3 minutes ethyl chlorothiocarbonate (0.15 g). The mixture was stirred at room temperature for 2 hours. To the solution was added water (30 ml). The mixture was extracted with diethylether (60 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to give 2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazine (0.21 g, yield: 60%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818640B1
Source datasetuspto-grants-2004_11
ORD IDord-3ea8d6f3882347bb87c2fb1a22691ec1
Source noteuspto-grants-2004_11