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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10326생성일: 2026년 10월 24일

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/ko/reaction/10326

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 번호US07094780B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-4df6972c6e4c48278a3fccf487f8d5a4
출처 메모uspto-grants-2006_08