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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1251348생성일: 2026년 10월 27일

Methyl iodide → 5-Nitro-1-methyl-uracil

https://huagongshe.com/reaction/1251348

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물5-Nitrouracil bis(trimethylsilyl)etherHCID 86751147—
용매DimethylformamideHCID 6228—
생성물5-Nitro-1-methyl-uracilHCID 2755734—

반응 단계

5-nitrouracil (10.00 g, 64 mmole), 1,1,1-3,3,3-hexamethyldisilazane (40 mL, 190 mmole) and chlorotrimethylsilane (4.0 mL, 32 mmole) are heated to reflux for 24 hours. The solution is concentrated under reduced pressure to afford 5-nitrouracil bis(trimethylsilyl)ether. 5-nitrouracil bis(trimethylsilyl)ether (10.0 g, 24 mmole), dimethylformamide (50 mL) and iodomethane (3.0 mL, 49 mmole) are heated in an 80° C. oil bath for 24 hours. Ice water is added, and the mixture is stirred for 30 minutes, then extracted with dichloromethane (3×). The combined organic layers are dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound. An alternative method of preparing the title compound is described in Example 108.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06342504B1
출처 데이터셋uspto-grants-2002_01
ORD IDord-71c1b0be71284a2895506f4cd35d2478
출처 메모uspto-grants-2002_01