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Sodium Hydroxide → 1-(pyridin-3-ylmethyl)piperidin-4-amine

HRID 972823
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HRID 972823 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][N:8]2[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]2)[CH:2]=1.Cl.O[NH3+:17].[OH-].[Na+].[Al]>C(O)C.[Ni]>[NH2:17][CH:11]1[CH2:12][CH2:13][N:8]([CH2:7][C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)[CH2:9][CH2:10]1
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참가 물질

7

반응물 4

HCID 14798Sodium HydroxideHCID 5359268AluminumHCID 64216241-(Pyridin-3-ylmethyl)piperidin-4-oneHCID 22029257Hydroxyammonium hydrochloride

생성물 1

HCID 64842041-(pyridin-3-ylmethyl)piperidin-4-amine

시약·촉매·용매 2

HCID 935Nickel촉매
HCID 702
Ethanol
용매

실험 절차

38.05 Grams of N-(3-pyridylmethyl)-4-piperidone and 27.8 grams of hydroxylammonium hydrochloride were dissolved in 600 milliliters of ethanol. 300 milliliters of 30% sodium hydroxide were added and the solution refluxed for half an hour, and then 40 grams of nickel, aluminium alloy were carefully added portionwise to the refluxing solution. The solution was refluxed for a further 3 hours, cooled and filtered through kieselguhr. The solution was evaporated and the residue treated with ether. The combined ether extracts were dried over magnesium sulphate and evaporated to give 33.72 grams of 4-amino-N-(3-pyridylmethyl)piperidine.

후처리

  1. temperaturethe solution refluxed for half an hour
  2. temperatureThe solution was refluxed for a further 3 hours
  3. temperaturecooled
  4. filtrationfiltered through kieselguhr
  5. customThe solution was evaporated
  6. additionthe residue treated with ether
  7. dry with materialThe combined ether extracts were dried over magnesium sulphate
  8. customevaporated

출처 및 근거

ORD 기록
ord-18cfbd80d4a14d689f7f2743336793c5
출처 데이터셋
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04053615

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