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Nitrogen → N,N-dimethyl-3-azabicyclo[3.2.1]octan-8-amine

HRID 1850563
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HRID 1850563 반응식
C([N:8]1[CH2:14][CH:13]2[CH:15]([N:16]([CH3:18])[CH3:17])[CH:10]([CH2:11][CH2:12]2)[CH2:9]1)C1C=CC=CC=1.N#N>CO.[Pd]>[CH3:17][N:16]([CH3:18])[CH:15]1[CH:13]2[CH2:12][CH2:11][CH:10]1[CH2:9][NH:8][CH2:14]2
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참가 물질

5

반응물 2

HCID 947NitrogenHCID 673554083-benzyl-N,N-dimethyl-3-azabicyclo[3.2.1]octan-8-amine

생성물 1

HCID 67356379N,N-dimethyl-3-azabicyclo[3.2.1]octan-8-amine수율 87%

시약·촉매·용매 2

HCID 23938Palladium촉매2회HCID 887Methanol용매

실험 절차

3-benzyl-N,N-dimethyl-3-azabicyclo[3.2.1]octan-8-amine (80 mg, 0.45 mmol) was dissolved in MeOH (10 ml) and the atmosphere was replaced with N2 (3×). 10% Pd/C (cat.) was added and the atmosphere was replaced with H2 (3×). The resulting reaction mixture was stirred at RT at balloon pressure overnight. When TLC showed no more UV active spot the Pd/C was filtered off (always keeping wet with MeOH) and the filtrate was concentrated which gave N,N-dimethyl-3-azabicyclo[3.2.1]octan-8-amine (44 mg) in 87% yield. 1H NMR (400 MHz, MeOD) δ ppm 3.45 (d, J=12.13 Hz, 2H) 2.88 (dd, J=12.38, 2.78 Hz, 2H) 2.35 (d, J=2.02 Hz, 2H) 2.31-2.23 (m, 6H) 2.11 (t, J=4.80 Hz, 1H) 2.06-1.92 (m, 2H) 1.89-1.79 (m, 2H)

후처리

  1. customThe resulting reaction mixture
  2. filtrationwas filtered off (
  3. concentrationwas concentrated which

출처 및 근거

ORD 기록
ord-a34a02fd57a94bbbbc4d9b779d361b7a
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08957074B2

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