Cesium carbonate → Methyl 4-(6-quinaldinyloxy)-3-methylsulfonyl-benzoate

HRID 1684560노트

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HRID 1684560 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([CH3:12])[CH:6]=[CH:5]2.Cl[C:14]1[CH:23]=[CH:22][C:17]([C:18]([O:20][CH3:21])=[O:19])=[CH:16][C:15]=1[S:24]([CH3:27])(=[O:26])=[O:25].C([O-])([O-])=O.[Cs+].[Cs+].C([O-])(O)=O.[Na+]>CN(C)C(=O)N(C)C>[N:8]1[C:9]2[C:4](=[CH:3][C:2]([O:1][C:14]3[CH:23]=[CH:22][C:17]([C:18]([O:20][CH3:21])=[O:19])=[CH:16][C:15]=3[S:24]([CH3:27])(=[O:25])=[O:26])=[CH:11][CH:10]=2)[CH:5]=[CH:6][C:7]=1[CH3:12]

참가 물질

6

실험 절차

2 g of 6-hydroxyquinaldine, 3.12 g of methyl 4-chloro-3-methylsulfonyl-benzoate and 12.28 g of Cs2CO3 are stirred in 50 ml of anhydrous tetramethylurea at 110° C. for 1 h. The mixture is cooled, 250 ml of saturated aqueous NaHCO3 solution are added and extraction is carried out 3 times with 125 ml of EA. The extracts are dried over Na2SO4, the solvent is removed in vacuo and the residue is chromatographed with MTB. 3.98 g of a colorless foam are obtained. Rf (MTB)=0.31 MS (ES): 372 (M+H)+

후처리

  1. temperatureThe mixture is cooled
  2. extractionextraction
  3. dry with materialThe extracts are dried over Na2SO4
  4. customthe solvent is removed in vacuo
  5. customthe residue is chromatographed with MTB

출처 및 근거

ORD 기록
ord-68c3d2c20f4043c88fa17be9786cd7ed
출처 데이터셋
uspto-grants-1997_06
특허 번호
US05641792

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