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HRID 38760作成日:2026年10月25日

2-Methyl-2-thiopseudourea sulfate → Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/38760

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-thiopseudourea sulfateHCID 75270—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Methyl pivaloylacetateHCID 99597—
反応物Sodium AcetateHCID 517045—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 58168926—

反応条件

温度75 °C

反応手順

A mixture of methyl 4,4-dimethyl-3-oxopentanoate (10 g) and N,N-dimethyl formamide dimethyl acetal (9.5 mL) was stirred at 75° C. for 2 hours. To the reaction mixture were added N,N-dimethyl formamide (100 mL), S-methylisothiourea sulfate (2:1) (9.7 g), and sodium acetate (11.4 g), followed by stirring at 90° C. for 15 hours. The reaction mixture was cooled to room temperature, and water was added thereto. The aqueous layer was extracted with ethyl acetate and the organic layer was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then filtered, and concentrated. The obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate (8.4 g) as a colorless oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524727B2
出典データセットuspto-grants-2013_09
ORD IDord-cf7b38d4db5847fe91ef4f679d98c286
出典メモuspto-grants-2013_09