HCID 59424354, compound → 3-(Piperidin-4-yl)quinolin-2(1H)-one

HRID 1172358Notes

Reaction equation

HRID 1172358 reaction equation
C([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:15](=[O:24])[NH:16][C:17]3[C:22]([CH:23]=2)=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>CO.[OH-].[OH-].[Pd+2]>[NH:8]1[CH2:9][CH2:10][CH:11]([C:14]2[C:15](=[O:24])[NH:16][C:17]3[C:22]([CH:23]=2)=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:12][CH2:13]1

Participants

5

Reactant 2

HCID 59424354HCID 59424354, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 183210463-(Piperidin-4-yl)quinolin-2(1H)-oneYield 90%

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 887MethanolSolvent

Procedure

3-(1-benzylpiperidin-4-yl)quinolin-2(1H)-one (5.40 mmol, 1.72 g) was suspended in methanol (70 mL). A catalytic amount of 20% palladium hydroxide on carbon was added to the mixture. The reaction vessel was placed on a Parr apparatus and charged with 55 psi of hydrogen gas. Reaction shook at room temperature for 5 hours. Mixture was removed from the apparatus and filtered. Filtrate was concentrated. Title compound was obtained as white solid in 90% yield. 1H NMR (300 MHz, DMSO-d6): δ=7.65 (s, 1H), 7.64 (d, J=10.61, 1H), 7.41 (t, J=7.50, 1H), 7.26 (d, J=8.05, 1H), 7.13 (t, J=7.32, 1H), 3.02 (d, J=11.71, 2H), 2.82 (t, J=11.89, 2H), 2.58 (t, J=11.71, 2H), 1.73 (t, J=11.71, 2H), 1.42 (m, 2H). MS m/e (M+H)+=229.4.

Workup

  1. customReaction
  2. customMixture was removed from the apparatus
  3. filtrationfiltered
  4. concentrationFiltrate was concentrated

Sources & evidence

ORD record
ord-f73b2b30c20b4d3c9a71b33171065af5
Source dataset
uspto-grants-2010_11
Patent number
US07834007B2

Reaction notes

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