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

HRID 2164208ノート

反応式

HRID 2164208 の反応式
[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

参加物

8

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-279d6f651ff7416586e4ef056c2d1fae
出典データセット
uspto-grants-1985_03
特許番号
US04502882

反応ノート

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