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8-Methylimidazo(1,2-a)pyridine → 8-Methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

HRID 2238645
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인쇄 미리보기

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HRID 2238645 반응식
[CH3:1][C:2]1[C:3]2[N:4]([CH:8]=[CH:9][N:10]=2)[CH:5]=[CH:6][CH:7]=1>C(O)CCC.[Ni]>[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]2[CH:8]=[CH:9][N:10]=[C:3]12
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참가 물질

4

반응물 1

HCID 3279578-Methylimidazo(1,2-a)pyridine

생성물 1

HCID 104417588-Methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine수율 79.9%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 2631-Butanol용매

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온도
65 °C

실험 절차

1 g of 8-methylimidazo[1,2-a]pyridine [3-1] was dissolved in 20 mL of 1-butanol, and a catalytic amount of Raney nickel of was added thereto. The mixture was stirred under a hydrogen atmosphere (5 atmospheric pressure) at 65° C. for 4 days. After cooling the reaction mixture back to room temperature, the insolubles were filtered through celite, and washed with methanol. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography, to obtain 823.3 mg of 8-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine [46-1].

후처리

  1. temperatureAfter cooling the reaction mixture back to room temperature
  2. filtrationthe insolubles were filtered through celite
  3. washwashed with methanol
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-8f3eeb8f5b18457c8a4ed2edf6b5570b
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718801B2

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