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HRID 33963作成日:2026年10月25日

Dimethylformamide → 3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one

https://huagongshe.com/reaction/33963

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl iodideHCID 6328—
反応物4-CyanopyridineHCID 7506—
反応物Ethyl 2-naphthylacetateHCID 256821—
反応物MethylthioisocyanateHCID 21933440—
反応物Potassium tert-butoxideHCID 23665647—
生成物3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-oneHCID 22346641—

反応手順

To a stirring solution of ethyl-2-naphthylacetate (10.0 g, 46.7 mmol) and 4-cyanopyridine (4.86 g, 46.7 mmol) in 50 mL dry dimethylformamide (DMF) at room temperature under nitrogen was added 47 mL potassium tert-butoxide (1.0 M in 2-methyl-2-propanol) dropwise via syringe. The dark red solution was stirred at room temperature for 75 min. Methylthioisocyanate (3.41 g, 46.7 mmol) in 10 mL DMF added whole. The solution was stirred for 90 min at room temperature. Iodomethane (2.95 mL, 46.7 mmol) was added dropwise over a 3 min period. Solid precipitates out of reaction. Continued to stir as a mixture for 30 min. Water (500 mL) was slowly added to reaction mixture. The solid was collected via filtration then washed with water, cold ethanol (50 mL), and ether. The solid was air dried for 3 days. M+1=360.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429594B2
出典データセットuspto-grants-2008_09
ORD IDord-77270c2e721440a28b95e897fee0bb01
出典メモuspto-grants-2008_09