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

HRID 1166285

반응식

HRID 1166285 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:12]([C:13]3[CH:14]=[CH:15][C:16]([S:19]([NH2:22])(=[O:21])=[O:20])=[CH:17][CH:18]=3)[N:11]=[C:10]([C:23]([F:26])([F:25])[F:24])[CH:9]=2)=[CH:6][CH:7]=1.Br[CH2:28][C:29]([O:31][CH3:32])=[O:30].[C:33]([O-:36])([O-])=O.[K+].[K+].[C:39]([O-])(O)=O.[Na+].CN([CH:47]=[O:48])C>>[CH3:32][O:31][C:29](=[O:30])[CH2:28][N:22]([S:19]([C:16]1[CH:15]=[CH:14][C:13]([N:12]2[C:8]([C:5]3[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=3)=[CH:9][C:10]([C:23]([F:24])([F:26])[F:25])=[N:11]2)=[CH:18][CH:17]=1)(=[O:21])=[O:20])[CH2:39][C:33]([O:48][CH3:47])=[O:36]

참가 물질

6

실험 절차

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, 3H); HRMS (M+NH4)+ calcd. for C23H26F3N4O6S: 543.1525; found: 543.1526.

후처리

  1. extractionextracted with ethyl acetate (200 mL)
  2. washThe ethyl acetate solution was then washed with sat NaCl (50 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. customThe crude product was purified by flash chromatography (silica gel, 98:2 methylene chloride:methanol)

출처 및 근거

ORD 기록
ord-c87862b54a0247bcb2a4b8c011a2bb06
출처 데이터셋
uspto-grants-2003_09
특허 번호
US06613790B2

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