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1'-Benzyl-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine] → 1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]

HRID 1665818
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인쇄 미리보기

반응식

HRID 1665818 반응식
C([N:8]1[CH2:13][CH2:12][C:11]2([C:17]3[CH:18]=[N:19][CH:20]=[CH:21][C:16]=3[CH2:15][O:14]2)[CH2:10][CH2:9]1)C1C=CC=CC=1>FC(F)(F)CO.[Pd]>[NH:8]1[CH2:9][CH2:10][C:11]2([C:17]3[CH:18]=[N:19][CH:20]=[CH:21][C:16]=3[CH2:15][O:14]2)[CH2:12][CH2:13]1
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참가 물질

4

반응물 1

HCID 597568161'-Benzyl-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]

생성물 1

HCID 467351631H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]수율 107.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 64092,2,2-Trifluoroethanol용매

실험 절차

A solution of 0.22 g (0.78 mmol) 1′-benzyl-1H-spiro[furo[3,4-c]pyridine-3,4′-piperidine] in 8 ml 2,2,2-trifluoroethanol was purged with argon prior to adding 0.08 g (10 mol %) palladium on activated charcoal. The flask was evacuated, refilled with hydrogen gas and stirred under an atmosphere of hydrogen gas for 20 h. The catalyst was filtered off and washed with ethanol. The filtrate was concentrated to dryness to give the title compound (0.16 g, quantitative, purity of approximately 95%) as a light yellow amorphous solid.

후처리

  1. customThe flask was evacuated
  2. additionrefilled with hydrogen gas
  3. filtrationThe catalyst was filtered off
  4. washwashed with ethanol
  5. concentrationThe filtrate was concentrated to dryness

출처 및 근거

ORD 기록
ord-b0db19bdea50450b804a7f6bdb7dc724
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08039624B2

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