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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200022Generated: November 2, 2026

4-Methoxy-alpha-toluenethiol → Methyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylate

https://huagongshe.com/reaction/1200022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-alpha-toluenethiolHCID 80407—
ReactantSodium methanolate methanolHCID 23694274—
Reactantmethyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylateHCID 86742402—
SolventMethanolHCID 887—
ProductMethyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylateHCID 1427762262.2%

Reaction Steps

A solution of 1.20 g (5 mmol) of methyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylate in 5 mL of methanol and 1.5 mL (6 mmol) of 4.1M sodium methoxide methanol was stirred at room temperature for 10 minutes. Then the solvent was concentrated and the residue was dissolved in 5 mL of N,N-dimethylformamide and 5 mL of tetrahydrofuran. 0.936 g (6 mmol) of p-methoxybenzylmercaptan was added and the solution was stirred at room temperature for 18 hours. The solution was partitioned between ether and water and the aqueous layer was extracted with two portions of ether. The combined extracts were washed with brine, dried and concentrated. Recrystallization from methanol afforded 0.90 g (62%) of pale tan needles, m.p. 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904672
Source datasetuspto-grants-1990_02
ORD IDord-1bbdfd64d0084f03be6964e2b024da6c
Source noteuspto-grants-1990_02