7-benzyloxy-1-[(2,2-dimethyl[1,3]dioxolan-4-yl)methyl]-2-ethoxymethyl-1H-imidazo[4,5-c]quinoline → 1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-ol

HRID 2203560노트

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HRID 2203560 반응식
C([O:8][C:9]1[CH:10]=[CH:11][C:12]2[C:13]3[N:21]([CH2:22][CH:23]4[CH2:27][O:26][C:25]([CH3:29])([CH3:28])[O:24]4)[C:20]([CH2:30][O:31][CH2:32][CH3:33])=[N:19][C:14]=3[CH:15]=[N:16][C:17]=2[CH:18]=1)C1C=CC=CC=1>C(#N)C.C(Cl)(Cl)Cl.CO.[OH-].[Pd+2].[OH-]>[CH3:28][C:25]1([CH3:29])[O:24][CH:23]([CH2:22][N:21]2[C:13]3[C:12]4[CH:11]=[CH:10][C:9]([OH:8])=[CH:18][C:17]=4[N:16]=[CH:15][C:14]=3[N:19]=[C:20]2[CH2:30][O:31][CH2:32][CH3:33])[CH2:27][O:26]1

참가 물질

5

실험 절차

Palladium hydroxide (Pearlman's catalyst) (20% wt. % palladium on carbon, 2.2 g) was added to a solution of 7-benzyloxy-1-[(2,2-dimethyl[1,3]dioxolan-4-yl)methyl]-2-ethoxymethyl-1H-imidazo[4,5-c]quinoline (22.2 g, 49.6 mmol) in acetonitrile (400 mL) and the reaction mixture was hydrogenated (30 psi, 2.1×105 Pa) for 24 hours on a Parr apparatus. The crude reaction mixture was diluted with 1:1 chloroform/methanol (1 L), then was filtered through a layer of CELITE filter agent. The filtrate was concentrated under reduced pressure and triturated with acetonitrile. The resulting crystalline material was collected by filtration, washed with acetonitrile, and dried to afford 16.55 g of 1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-ol as a white powder, mp 239-240° C.

후처리

  1. customfor 24 hours
  2. customThe crude reaction mixture
  3. filtrationwas filtered through a layer of CELITE filter agent
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customtriturated with acetonitrile
  6. filtrationThe resulting crystalline material was collected by filtration
  7. washwashed with acetonitrile
  8. customdried

출처 및 근거

ORD 기록
ord-5b15182092a640f1b7250dacd040ea9a
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09365567B2

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