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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154757Generated: November 3, 2026

Pyridine → methyl N-[methyl(phenylsulfinothioyl)carbamoyl]oxyethanimidothioate

https://huagongshe.com/reaction/1154757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethomylHCID 4109—
ReactantThiophenolHCID 7969—
ReactantThionyl ChlorideHCID 24386—
SolventTetrahydrofuranHCID 8028—
Productmethyl N-[methyl(phenylsulfinothioyl)carbamoyl]oxyethanimidothioateHCID 131712178—

Reaction Steps

A mixture of 3.3 g S-methyl N-[N'-methylcarbamoyloxy]thioacetimidate (0.02 mol), 1.9 g pyridine (0.024 mol) and 2.5 g thionyl chloride (0.021 mol), in 20 ml dry tetrahydrofuran was stirred at room temperature for 4 hours. Pyridine (1.9 g, 0.024 mol) was added and followed by 2.2 g benzenethiol (0.02 mol) added dropwise at water bath temperature. Stirring was continued for an additional hour, and the mixture was worked up as described for Example I. The resulting oily residue was purified by preparative thin-layer chromatography, and the NMR spectrum obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298527
Source datasetuspto-grants-1981_11
ORD IDord-00e4e54555514467b7762893811c0136
Source noteuspto-grants-1981_11