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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550561생성일: 2026년 10월 24일

Ethyl Acetate → N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamide

https://huagongshe.com/ko/reaction/550561

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물5-Amino-4-cyanopyrazoleHCID 85515—
반응물N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl)-N-ethyl-methanesulfonamideHCID 67198287—
용매Acetic AcidHCID 176—
생성물N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamideHCID 1165303652.4%

반응 단계

A mixture of 0.196 g (1.82 mmol) of 4-cyano-2H-pyrazol-3-ylamine and 0.54 g (1.82 mmol) of N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl]-N-ethyl-methanesulfonamide in 10 ml of glacial acetic acid was refluxed for 8 hours and then the solvent was removed by reduced pressure distillation. To the resulting residue were added 10 ml of dichloromethane and 10 ml of saturated sodium bicarbonate solution. The two layers were separated, and the aqueous layer was washed with 10 ml of dichloromethane. The organic layers were washed with 10 ml of water and dried over magnesium sulfate. The dichloromethane layer was evaporated to dryness to yield an oil which, in the presence of ethyl acetate, gave 324 mg of N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamide as a yellow solid (yield 52.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947688B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-e032f0561f5749b7b00f522d40231695
출처 메모uspto-grants-2011_05