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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-Hydroxy-2,4-dinitrobenzenamine | HCID 5743493 | — |
| 반응물 | 1-Cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid | HCID 21979364 | — |
| 용매 | 1,4-dioxane N,N-dimethylformamide | HCID 21712069 | — |
| 생성물 | 3-Amino-1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid | HCID 21979001 | 76.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094780B1 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-4df6972c6e4c48278a3fccf487f8d5a4 |
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| 출처 메모 | uspto-grants-2006_08 |
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