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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 729412생성일: 2026년 10월 25일

Sodium hydride → 3-Amino-1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid

https://huagongshe.com/reaction/729412

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물N-Hydroxy-2,4-dinitrobenzenamineHCID 5743493—
반응물1-Cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acidHCID 21979364—
용매1,4-dioxane N,N-dimethylformamideHCID 21712069—
생성물3-Amino-1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acidHCID 2197900176.7%

반응 단계

A solution of 0.47 g (1.57 mmol) of 1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid (Example 35) in 20 mL of dimethylformamide/dioxane (1:1) is treated portionwise with 0.08 g (2.0 mmol) of 60% sodium hydride/mineral oil. The reaction is stirred at room temperature for 1 hour and 0.32 g (1.6 mmol) of 2,4-dinitrophenylhydroxylamine is added all at once. After stirring at room temperature overnight, the dioxane is removed in vacuo and the residue is diluted to 100 mL with ice and water and stirred at 5° C. for 1 hour. The aqueous solution is extracted with ethyl acetate (3×50 mL) with the combined organic layers being washed with water, dried (MgSO4), filtered and evaporated in vacuo to give 0.4 g of the title compound, mp 167-169° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582627B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-f4e374bda43a4f4daae39c5427da66a4
출처 메모uspto-grants-2009_09