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HCID 20430878, 화합물 → 5-(4-Fluorobenzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

HRID 2413348
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HRID 2413348 반응식
C([O:5][C:6]([CH:8]1[CH2:12][CH2:11][N:10]2[C:13]([C:23](=[O:31])[C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=3)=[CH:14][C:15](C(OC(C)(C)C)=O)=[C:9]12)=[O:7])(C)(C)C>FC(F)(F)C(O)=O>[F:30][C:27]1[CH:28]=[CH:29][C:24]([C:23]([C:13]2[N:10]3[CH2:11][CH2:12][CH:8]([C:6]([OH:7])=[O:5])[C:9]3=[CH:15][CH:14]=2)=[O:31])=[CH:25][CH:26]=1
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참가 물질

3

반응물 1

HCID 20430878HCID 20430878, 화합물

생성물 1

HCID 129159145-(4-Fluorobenzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

t-Butyl-5-(p-fluorobenzoyl)-7-t-butoxycarbonyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylate (1 mmole) is dissolved in 5 ml of trifluoroacetic acid. The reaction mixture is heated at reflux for 5 hours before it is evaporated in vacuo to remove most of the solvent. The resulting oil is triturated with about 10 ml of water, filtered and dried in vacuo to afford 5-(p-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid.

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureat reflux for 5 hours before it
  • customis evaporated in vacuo
  • customto remove most of the solvent
  • customThe resulting oil is triturated with about 10 ml of water
  • filtrationfiltered
  • customdried in vacuo
  • 출처 및 근거

    ORD 기록
    ord-ffb313a7db024ad097826347239f5fa6
    출처 데이터셋
    uspto-grants-1985_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04496741

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