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4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde → 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]piperidine

HRID 1388409
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HRID 1388409 반응식
[CH3:1][C:2]1[N:3]([CH2:7][CH2:8][CH2:9][CH:10]2[CH2:15][CH2:14][N:13](C=O)[CH2:12][CH2:11]2)[CH:4]=[CH:5][N:6]=1>O1CCOCC1.Cl>[CH3:1][C:2]1[N:3]([CH2:7][CH2:8][CH2:9][CH:10]2[CH2:11][CH2:12][NH:13][CH2:14][CH2:15]2)[CH:4]=[CH:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 202397824-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde

생성물 1

HCID 202397544-[3-(2-methyl-1H-imidazol-1-yl)propyl]piperidine수율 68.7%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

A mixture of 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde (3.8 g, 0.016 M) in dioxane (100 ml) and 2 N HCl (25 ml) was heated and refluxed for 51/2 hrs. After this period, solvent was removed, and 1 N NaOH (50 ml) was added to the residue. This mixture was then extracted with methylene chloride (5×50 ml). The combined extracts, dried over sodium sulfate, were stripped to dryness to yield 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]piperidine (2.3 g, 65% yield).

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후처리

  1. temperaturewas heated
  2. temperaturerefluxed for 51/2 hrs
  3. waitAfter this period
  4. customsolvent was removed
  5. addition1 N NaOH (50 ml) was added to the residue
  6. extractionThis mixture was then extracted with methylene chloride (5×50 ml)
  7. dry with materialThe combined extracts, dried over sodium sulfate

출처 및 근거

ORD 기록
ord-caf0f7889f204b8489a7b49e87a3da8b
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04431653

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