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Trifluoroacetic acid → HCID 23442300, 화합물

HRID 2119664
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HRID 2119664 반응식
[CH3:1][N:2]1[C:14]2[C:13](=[O:15])[C:12]3[CH:11]=[C:10]([CH3:16])[CH:9]=[CH:8][C:7]=3[N:6]([CH:17]3[CH2:22][CH2:21][N:20](C(OC(C)(C)C)=O)[CH2:19][CH2:18]3)[C:5]=2[CH:4]=[N:3]1.FC(F)(F)C(O)=O>ClCCl>[CH3:1][N:2]1[C:14]2[C:13](=[O:15])[C:12]3[CH:11]=[C:10]([CH3:16])[CH:9]=[CH:8][C:7]=3[N:6]([CH:17]3[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]3)[C:5]=2[CH:4]=[N:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 23442453HCID 23442453, 화합물

생성물 1

HCID 23442300HCID 23442300, 화합물수율 47%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
45 °C

실험 절차

To a solution of tert-butyl 4-(1,7-dimethyl-9-oxo-1,9-dihydro-4H-pyrazolo[4,3-b]quinolin-4-yl)-1-piperidinecarboxylate (EXAMPLE 64, step 1, 62 mg, 0.16 mmol) in dichloromethane (5 ml) was added trifluoroacetic acid (0.03 ml, 0.39 mmol) and the mixture was stirred at room temperature for 7 h and at 45° C. for 21 h. After evaporation, the residue was dissolved in dichloromethane (20 ml), washed with saturated aqueous sodium bicarbonate (20 ml) and dried over sodium sulfate. Removal of solvent gave 22 mg (47%) of the title compound as a white solid.

후처리

  1. customAfter evaporation
  2. dissolutionthe residue was dissolved in dichloromethane (20 ml)
  3. washwashed with saturated aqueous sodium bicarbonate (20 ml)
  4. dry with materialdried over sodium sulfate
  5. customRemoval of solvent

출처 및 근거

ORD 기록
ord-dfe25be50c6a4fa2b6e8019bbbf1e8df
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06686373B2

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