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Phosphorus oxychloride → HCID 58739136, 화합물

HRID 720235
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HRID 720235 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:11]2[S:12][C:13]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)=[CH:14][C:10]=2[C:9](=O)[NH:8][N:7]=1)=[O:5])[CH3:2].P(Cl)(Cl)([Cl:25])=O>>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[N:8][C:9]([Cl:25])=[C:10]2[CH:14]=[C:13]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[S:12][C:11]=12)=[O:5])[CH3:2]
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 58739134HCID 58739134, 화합물

생성물 1

HCID 58739136HCID 58739136, 화합물

반응 조건

온도
90 °C

실험 절차

A mixture of 2-(4-fluoro-phenyl)-4-oxo-4,5-dihydro-thieno[2,3-d]pyridazine-7-carboxylic acid ethyl ester (0.2 g, mmol) in phosphorous oxychloride (3 mL) was heated at 90° C. for 3 hours, cooled and evaporated to dryness. To the residue was added ice and ethyl acetate and then basified over potassium carbonate solid. The organic layer was separeted, washed with water, brine and dried over sodium sulfate. The organic layer was evaporated to dryness and the residue was purified by flash chromatography (silica gel, 5% acetone/hexane) to obtain 4-chloro-2-(4-fluorophenyl)-thieno[2,3-d]pyridazine-7-carboxylic acid ethyl ester as a solid (0.12 g). MS: m/z=338 (M+1).

후처리

temperature
cooled
  • customevaporated to dryness
  • additionTo the residue was added ice and ethyl acetate
  • washwashed with water, brine
  • dry with materialdried over sodium sulfate
  • customThe organic layer was evaporated to dryness
  • customthe residue was purified by flash chromatography (silica gel, 5% acetone/hexane)
  • 출처 및 근거

    ORD 기록
    ord-f07bbfca8166423784ea9b751db53faa
    출처 데이터셋
    uspto-grants-2006_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07135470B2

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