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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1668539생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1668539

반응식

참여 물질

역할이름HCID투입량
반응물Diisopropyl EtherHCID 7914—
반응물N-(4-(2,2-Dicyanoethenyl)phenyl)acetamideHCID 33296—
반응물N-bromobutanimideHCID 67184—
반응물Sodium BicarbonateHCID 516892—
반응물ThioureaHCID 2723790—
용매EthanolHCID 702—
생성물N-{4-[6-amino-5-cyano-2-(6-methylpyridin-2-ylmethylsulfanyl)pyrimidin-4-yl]phenyl}acetamideHCID 11581892—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989446B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-9b5a915edc4941cb944ab391151d2d46
출처 메모uspto-grants-2011_08