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HCID 178487720、化合物 → Isoxazolo(4,5-c)quinolin-3(2H)-one, 7-methoxy-2-phenyl-

HRID 280110
ノート
印刷プレビュー

反応式

HRID 280110 の反応式
O[N:2]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:3]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1[OH:15])=[CH:12][CH:11]=[C:10]([O:16][CH3:17])[CH:9]=2)=[O:4]>O>[CH3:17][O:16][C:10]1[CH:11]=[CH:12][C:13]2[C:14]3[O:15][N:2]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:3](=[O:4])[C:5]=3[CH:6]=[N:7][C:8]=2[CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 178487720HCID 178487720、化合物

生成物 1

HCID 13669238Isoxazolo(4,5-c)quinolin-3(2H)-one, 7-methoxy-2-phenyl-収率 20.2%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Using the procedure of Step B of Example 2, 3.68 g of N,4-dihydroxy-7-methoxy-N-phenyl-3-quinoline carboxamide were reacted and after 18 hours at ambient temperature, the reaction mixture was poured into water and the products which crystallized were extracted with dichloromethane. The organic phase was washed with water and the solvent was eliminated. The residue was chromatographed on silica and eluted with a mixture of methylene chloride-ethyl acetate (9-1) to obtain 0.7 g of 7-methoxy-2-phenylisoxazolo(4,5-c)quinolin-3-(2H)-one melting at 170° C.

後処理

  1. customwere reacted and after 18 hours at ambient temperature
  • customthe products which crystallized
  • extractionwere extracted with dichloromethane
  • washThe organic phase was washed with water
  • customThe residue was chromatographed on silica
  • washeluted with a mixture of methylene chloride-ethyl acetate (9-1)
  • 出典と根拠

    ORDレコード
    ord-60f56b67aef84d349a812300cd540fd3
    出典データセット
    uspto-grants-1986_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04588731

    反応ノート

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