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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393860생성일: 2026년 10월 25일

Celecoxib → Methyl N-(2-Methoxy-2-oxoethl)-N-({4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}sulfonyl)glycinate

https://huagongshe.com/reaction/393860

반응식

참여 물질

역할이름HCID투입량
반응물CelecoxibHCID 2662—
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물Methyl bromoacetateHCID 60984—
반응물Sodium BicarbonateHCID 516892—
생성물Methyl N-(2-Methoxy-2-oxoethl)-N-({4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}sulfonyl)glycinateHCID 2264764551%

반응 단계

A mixture of Celecoxib (0.500 g, 1.31 mmol), methyl bromoacetate (0.501 g, 3.28 mmol) and K2CO3 (0.362 g, 2.62 mmol) in anhydrous DMF (5.0 mL) was stirred at room temperature for 21 hours. The mixture was then poured into sat. NaHCO3 (200 mL) and extracted with ethyl acetate (200 mL). The ethyl acetate solution was then washed with sat NaCl (50 mL), dried over MgSO4, filtered and concentrated under vacuum. The crude product was purified by flash chromatography (silica gel, 98:2 methylene chloride:methanol) to afford 0.350 g (51% yield) of the product as a colorless glass: 1H NMR (dmso-d6/300 MHz) δ 7.90 (d, 2H, J=8.7 Hz), 7.53 (d, 2H, J=8.7 Hz), 7.23-7.17 (m, 5H), 4.19 (s, 4H), 3.54 (s, 6H), 2.30 (s, 31H); HRMS (M+NH4)+ calcd. for C23H26F3N4O6S: 543.1525; found: 543.1526.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809111B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-e819c016cfd94453b1fd6abf05e5e7ab
출처 메모uspto-grants-2004_10