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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084745Generated: October 31, 2026

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

https://huagongshe.com/reaction/1084745

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.lM 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 numberUS05006532
Source datasetuspto-grants-1991_04
ORD IDord-471ca076e5854011bd88dfe4edb17758
Source noteuspto-grants-1991_04