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

HRID 280110
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HRID 280110 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178487720HCID 178487720, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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.

후처리

  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)
  • 출처 및 근거

    ORD 기록
    ord-60f56b67aef84d349a812300cd540fd3
    출처 데이터셋
    uspto-grants-1986_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04588731

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