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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2298생성일: 2026년 10월 24일

Methanol → 4-tert-butyl-N-{6-[2-(5-ethynylpyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide

https://huagongshe.com/ko/reaction/2298

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Potassium CarbonateHCID 11430—
반응물4-tert-butyl-N-{6-[2-(5-trimethylsilylethynylpyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamideHCID 19689523—
용매Ammonium ChlorideHCID 25517—
생성물4-tert-butyl-N-{6-[2-(5-ethynylpyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamideHCID 1968945985.3%

반응 조건

온도0 °C

반응 단계

A mixture of 4-tert-butyl-N-{6-[2-(5-trimethylsilylethynylpyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide (667 mg), potassium carbonate (299 mg) and dry methanol (13 ml) is stirred at 0° C. for two hours, and diluted with saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The organic layer is washed with water and brine, dried over sodium sulfate, and filtered. The filtrate is concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (solvent; chloroform/ethyl acetate=30:1) to give 4-tert-butyl-N-{6-[2-(5-ethynylpyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}-benzenesulfonamide (502 mg) as colorless crystalline powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728706
출처 데이터셋uspto-grants-1998_03
ORD IDord-ef654fd56d444338b74762628d0ff15f
출처 메모uspto-grants-1998_03