Water → N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,3-benzoxathiole-4-sulfonamide

HRID 2164208노트

반응식

HRID 2164208 반응식
[O:1]1[C:5]2=[CH:6][CH:7]=[CH:8][C:9]([S:10]([NH2:13])(=[O:12])=[O:11])=[C:4]2[S:3][CH2:2]1.C[Al](C)C.[CH3:18][O:19][C:20]1[CH:25]=[C:24]([CH3:26])[N:23]=[C:22]([NH:27][C:28](=O)[O:29]C)[N:21]=1.O>C(Cl)Cl.Cl.C(O)(=O)C>[CH3:18][O:19][C:20]1[CH:25]=[C:24]([CH3:26])[N:23]=[C:22]([NH:27][C:28]([NH:13][S:10]([C:9]2[CH:8]=[CH:7][CH:6]=[C:5]3[O:1][CH2:2][S:3][C:4]=23)(=[O:12])=[O:11])=[O:29])[N:21]=1

참가 물질

8

실험 절차

To a solution of b 2,2 g 1,3-benzoxathiole-4-sulfonamide, prepared in Example 13, in 50 ml methylene chloride at ambient temperature under nitrogen is added 5.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature, 2.0 g of methyl [4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, is added and the reaction mixture is heated at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid, and 10 drops hydrochloric acid are sequentially added. The organic phase is separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gives a solid.

후처리

  1. additionis added
  2. temperaturethe reaction mixture is heated
  3. temperatureat reflux for 16 hours
  4. temperatureThe reaction mixture is cooled to ambient temperature
  5. customThe organic phase is separated
  6. customdried
  7. customthe solvent removed under reduced pressure
  8. customto give an oil
  9. customCrystallization of the oil from n-butyl chloride/ether
  10. customgives a solid

출처 및 근거

ORD 기록
ord-279d6f651ff7416586e4ef056c2d1fae
출처 데이터셋
uspto-grants-1985_03
특허 번호
US04502882

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