Acetic Acid → 3-[3-(6-Methoxy-3,4-xylyl)-1,2-benzisothiazol-5-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione

HRID 369583노트

반응식

HRID 369583 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][N:8]=[C:7]([C:10]3[C:15]([O:16][CH3:17])=[CH:14][C:13]([CH3:18])=[C:12]([CH3:19])[CH:11]=3)[C:6]=2[CH:20]=1.CN(C)[C:23]1[O:24][C:25](=[O:33])[CH:26]=[C:27]([C:29]([F:32])([F:31])[F:30])[N:28]=1.C(O)(=O)C.O>C(Cl)Cl.C(OCC)C>[CH3:17][O:16][C:15]1[C:10]([C:7]2[C:6]3[CH:20]=[C:2]([N:1]4[C:25](=[O:33])[CH:26]=[C:27]([C:29]([F:32])([F:31])[F:30])[NH:28][C:23]4=[O:24])[CH:3]=[CH:4][C:5]=3[S:9][N:8]=2)=[CH:11][C:12]([CH3:19])=[C:13]([CH3:18])[CH:14]=1

참가 물질

7

실험 절차

A mixture of 5-amino-3-(6-methoxy-3,4-xylyl)-1,2-benzisothiazole (8.53 g, 30.0 mmol), 2-dimethylamino-4-(trifluoromethyl)-6H-1,3-oxazin-6-one (6.87 g, 33.0 mmol) and acetic acid is refluxed for 2 hours, cooled, and poured into water. The resultant aqueous mixture is filtered to obtain a solid. A solution of the solid in methylene chloride is washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain an oil. Column chromatography of the oil using silica gel and a 5% diethyl ether in methylene chloride solution gives the title product as a yellow foam (8.37 g, 62.0%) which is identified by NMR spectral analyses.

후처리

  1. temperatureis refluxed for 2 hours
  2. temperaturecooled
  3. filtrationThe resultant aqueous mixture is filtered
  4. customto obtain a solid
  5. washA solution of the solid in methylene chloride is washed sequentially with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customto obtain an oil

출처 및 근거

ORD 기록
ord-89b019a7706847d5b77139add603e86f
출처 데이터셋
uspto-grants-2000_10
특허 번호
US06140270

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