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

HRID 1252871Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1252871
[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

Komponenten

8

Versuchsvorschrift

To a solution of 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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-017b29d4913044e5a5dfdc1cda7dd086
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04746358

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