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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81954생성일: 2026년 10월 27일

Methanesulfonyl chloride → N-(2,6-Diethylphenyl)-1-methyl-8-{[1-(methylsulfonyl)piperidin-4-yl]amino}-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

https://huagongshe.com/reaction/81954

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물N-(2,6-diethylphenyl)-1-methyl-8-(piperidin-4-ylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide hydrochlorideHCID 44555920—
용매DichloromethaneHCID 6344—
생성물N-(2,6-Diethylphenyl)-1-methyl-8-{[1-(methylsulfonyl)piperidin-4-yl]amino}-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 6707606864%

반응 단계

To a solution of N-(2,6-diethylphenyl)-1-methyl-8-(piperidin-4-ylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide hydrochloride (40 mg, 0.075 mmol) in dichloromethane (1 mL) at 0° C., DIPEA (0.2 mL, 1.1 mmol), and methanesulfonyl chloride (0.007 mL, 0.009 mmol) were added. The mixture was then stirred at room temperature for 3 h. Solvent evaporated to dryness and the crude solid was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol: 97/3) to 26 mg of the title compound. (64% yield)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846701B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-dbed34b1567c406dbf01dd954d3160b1
출처 메모uspto-grants-2014_09