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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350637Generated: October 25, 2026

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

https://huagongshe.com/reaction/350637

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 numberUS07183275B2
Source datasetuspto-grants-2007_02
ORD IDord-7a469e139c884c078235231610693182
Source noteuspto-grants-2007_02