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Acetic Acid → 1-azetidin-3-yl-N,N-dimethylpiperidine-4-carboxamide

HRID 426089
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HRID 426089 반응식
C1(C(C2C=CC=CC=2)[N:8]2[CH2:11][CH:10]([N:12]3[CH2:17][CH2:16][CH:15]([C:18]([N:20]([CH3:22])[CH3:21])=[O:19])[CH2:14][CH2:13]3)[CH2:9]2)C=CC=CC=1.C(O)(=O)C>CO.[OH-].[OH-].[Pd+2]>[NH:8]1[CH2:11][CH:10]([N:12]2[CH2:17][CH2:16][CH:15]([C:18]([N:20]([CH3:22])[CH3:21])=[O:19])[CH2:14][CH2:13]2)[CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 236589531-[1-(diphenylmethyl)azetidin-3-yl]-N,N-dimethylpiperidine-4-carboxamide

생성물 1

HCID 236587821-azetidin-3-yl-N,N-dimethylpiperidine-4-carboxamide수율 98.2%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

Palladium hydroxide on carbon (0.10 g) was placed in a 5 mL vial intended for microwave synthesis. 1-[1-(Diphenylmethyl)azetidin-3-yl]-N,N-dimethylpiperidine-4-carboxamide (0.20 g, 0.53 mmol) dissolved in methanol (3 mL) and acetic acid (0.3 mL) was added. The mixture was stirred under hydrogen (1.6 bar) at RT for four days. The mixture was filtered through a plug of Celite®. The solvent was removed by evaporation and there was obtained 0.11 g (53%) of the title compound.

후처리

  1. customvial intended for microwave synthesis
  2. filtrationThe mixture was filtered through a plug of Celite®
  3. customThe solvent was removed by evaporation

출처 및 근거

ORD 기록
ord-ef31420606c14d549d60556f318a9465
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106208B2

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