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HRID 1463244作成日:2026年10月27日

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

https://huagongshe.com/reaction/1463244

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium methanethiolateHCID 4378561—
反応物6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690700—
溶媒MethanolHCID 887—
生成物5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinoneHCID 19690712—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05300477
出典データセットuspto-grants-1994_04
ORD IDord-377906cb16a849deaf5e8ad5fe6ba6e2
出典メモuspto-grants-1994_04