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HRID 1668539作成日:2026年10月24日

Diisopropyl Ether → N-{4-[6-amino-5-cyano-2-(6-methylpyridin-2-ylmethylsulfanyl)pyrimidin-4-yl]phenyl}acetamide

https://huagongshe.com/ja/reaction/1668539

反応式

関与物質

役割名称HCID仕込み量
反応物Diisopropyl EtherHCID 7914—
反応物N-(4-(2,2-Dicyanoethenyl)phenyl)acetamideHCID 33296—
反応物N-bromobutanimideHCID 67184—
反応物Sodium BicarbonateHCID 516892—
反応物ThioureaHCID 2723790—
溶媒EthanolHCID 702—
生成物N-{4-[6-amino-5-cyano-2-(6-methylpyridin-2-ylmethylsulfanyl)pyrimidin-4-yl]phenyl}acetamideHCID 11581892—

反応手順

The portion (4.56 g) was dissolved in 50 mL of ethanol, 1.72 g of thiourea was added to the solution, and the mixture was heated to reflux for 1 hour. Next, to the reaction solution added 20 mL of ethanol and the solution was cooled, and further 4.79 g of N-[4-(2,2-dicyanovinyl)phenyl]acetamide and 3 g of sodium bicarbonate were added thereto, and then the mixture was heated to reflux for 1.5 hours. After the reaction solution was allowed to cool, 2.02 g of NBS was added to the solution, and the mixture was heated to reflux for 30 minutes. After reaction solution was allowed to cool, furthermore diisopropyl ether was added thereto, and the inorganic material precipitated was filtrated off, then the filtrate was again concentrated and dissolved in ethanol. Saturated aqueous sodium bicarbonate was added to the solution and the resulting crystal was filtrated, washed with water and ethanol, and then dried under reduced pressure to give 3.2 g of N-{4-[6-amino-5-cyano-2-(6-methylpyridin-2-ylmethylsulfanyl)pyrimidin-4-yl]phenyl}acetamide as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07989446B2
出典データセットuspto-grants-2011_08
ORD IDord-9b5a915edc4941cb944ab391151d2d46
出典メモuspto-grants-2011_08