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Phosphorus oxychloride → 1-ethyl-4-chloro-6-(methylthio)-1H-pyrazolo[3,4-b]quinoline

HRID 375901
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HRID 375901 반응식
[CH2:1]([N:3]1[C:7]([NH:8][C:9]2[C:10](=[CH:14][C:15]([S:18][CH3:19])=[CH:16][CH:17]=2)[C:11](O)=O)=[CH:6][CH:5]=[N:4]1)[CH3:2].O=P(Cl)(Cl)[Cl:22]>O>[CH2:1]([N:3]1[C:7]2=[N:8][C:9]3[C:10]([C:11]([Cl:22])=[C:6]2[CH:5]=[N:4]1)=[CH:14][C:15]([S:18][CH3:19])=[CH:16][CH:17]=3)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 21217703N-(1-ethylpyrazol-5-yl)-5-(methylthio)anthranilic acid

생성물 1

HCID 212177171-ethyl-4-chloro-6-(methylthio)-1H-pyrazolo[3,4-b]quinoline

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of N-(1-ethylpyrazol-5-yl)-5-(methylthio) anthranilic acid (4.5 g) and POCl3 (20 mL) was refluxed overnight. The reaction mixture was poured into water, then ice was added. The mixture was extracted with CH2Cl2 and then the CH2Cl2 layer was evaporated. The residue was purified by column chromatography on silica gel eluting with 50% ethyl acetate/hexane to afford 2.4 g of 1-ethyl-4-chloro-6-(methylthio)-1H-pyrazolo[3,4-b]quinoline, m.p. 120°-121° C.

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후처리

  1. temperaturewas refluxed overnight
  2. additionice was added
  3. extractionThe mixture was extracted with CH2Cl2
  4. customthe CH2Cl2 layer was evaporated
  5. customThe residue was purified by column chromatography on silica gel eluting with 50% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-0a1660df785c4f4eb149a954ccb2ee9a
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05488055

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