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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1082292생성일: 2026년 10월 24일

1,3-Dimethyl-2-imidazolidinone → 4-tert-butyl-N-{6-[2-(5-cyanopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide

https://huagongshe.com/ko/reaction/1082292

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dimethyl-2-imidazolidinoneHCID 6661—
반응물4-tert-butyl-N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamideHCID 9938571—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매HCID 178418397HCID 178418397—
용매Ammonium ChlorideHCID 25517—
생성물4-tert-butyl-N-{6-[2-(5-cyanopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamideHCID 19689463—

반응 조건

온도80 °C

반응 단계

A mixture of 4-tert-butyl-N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide (1.00 g), zinc cyanide (784 mg), tetrakis(triphenylphosphine)palladium (250 mg) and 1,3-dimethyl-2-imidazolidinone (40 ml) is stirred at 80° C. for 6 hours under argon atmosphere. The mixture is cooled to room temperature, and diluted with saturated aqueous ammonium chloride solution. The mixture is extracted with ethyl acetate, and the organic layer is washed with water (twice) 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=10:1) and recrystallized from tetrahydrofuran/ethyl acetate to give 4-tert-butyl-N-{6-[2-(5-cyanopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide (590 mg) as colorless crystalline powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05589478
출처 데이터셋uspto-grants-1996_12
ORD IDord-7496e99402ea46ba895d8a9f52352f13
출처 메모uspto-grants-1996_12