Water → HCID 20137751、化合物

HRID 542689ノート

反応式

HRID 542689 の反応式
[S:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([S:11]([NH2:14])(=[O:13])=[O:12])[C:5]=2[S:4][CH2:3][CH2:2]1.C[Al](C)C.C[O:20][C:21](=O)[NH:22][C:23]1[N:28]=[C:27]([O:29][CH3:30])[CH:26]=[C:25]([CH3:31])[N:24]=1.O>C(Cl)Cl.Cl.C(O)(=O)C>[CH3:30][O:29][C:27]1[CH:26]=[C:25]([CH3:31])[N:24]=[C:23]([NH:22][C:21]([NH:14][S:11]([C:10]2[C:5]3[S:4][CH2:3][CH2:2][S:1][C:6]=3[CH:7]=[CH:8][CH:9]=2)(=[O:12])=[O:13])=[O:20])[N:28]=1

参加物

8

反応物 4

HCID 962WaterHCID 13072161Methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 16682925TrimethylaluminumHCID 201377482,3-Dihydro-1,4-benzodithiine-5-sulfonamide

生成物 1

HCID 20137751HCID 20137751、化合物

試薬・触媒・溶媒 3

HCID 313Hydrochloric Acid触媒HCID 176Acetic Acid溶媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of 2.5 g 1,4-benzodithian-5-sulfonamide, prepared in Example 18, 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. customprepared
  2. additionis added
  3. temperaturethe reaction mixture is heated
  4. temperatureat reflux for 16 hours
  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-8a9bfbafeef941fcb1cf3d05c847ea90
出典データセット
uspto-grants-1987_04
特許番号
US04659368

反応ノート

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