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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463244Generated: October 26, 2026

Sodium methanethiolate → 5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1463244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690700—
SolventMethanolHCID 887—
Product5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinoneHCID 19690712—

Reaction Steps

To a solution of 2.5 g (9.67 mmol) of 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 100 mL of methanol, was added 0.8 g (11.4 mmol) sodium thiomethoxide and the reaction was stirred at room temperature for 4 days. The methanol was evaporated and the residue was dissolved in 100 mL of ethyl acetate, then washed three times with 50 mL of 1M sodium hydroxide followed by one time with 50 mL of brine. The organic layer was dried over MgSO4 and concentrated to yield 2.6 g crude product. Flash column chromatography on silica gel (100% methylene chloride) afforded 5-methyl-2-phenyl-3-propargyl-6-thiomethyl-4(3H)-pyrimidinone (Compound 26) as a white solid. 1H-NMR (CDCl3) δ2.1 (3H, s); 2.35 (1H, t); 2.5 (3H, s); 4.55 (2H, d); 7.5 (3H, m); 7.7 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300477
Source datasetuspto-grants-1994_04
ORD IDord-377906cb16a849deaf5e8ad5fe6ba6e2
Source noteuspto-grants-1994_04