N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline → 1-(1-Benzoyl-piperidin-4-yl)-3,4-dihydro-1H-quinolin-2-one

HRID 266787Notes

Reaction equation

HRID 266787 reaction equation
[C:1]([N:9]1[CH2:14][CH2:13][CH:12]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH2:22][CH2:23][C:24](=[O:26])N)[CH2:11][CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>Cl>[C:1]([N:9]1[CH2:10][CH2:11][CH:12]([N:15]2[C:16]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[CH2:22][CH2:23][C:24]2=[O:26])[CH2:13][CH2:14]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 1

HCID 19031102N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline

Product 1

HCID 149695101-(1-Benzoyl-piperidin-4-yl)-3,4-dihydro-1H-quinolin-2-oneYield 43.3%

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

To N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline (85 g) prepared in Reference Example 4 is added 5% hydrochloric acid (500 ml) and the mixture is refluxed for 5 hours. After cooling, the reaction mixture is extracted with diethyl ether and the aqueous layer is made alkaline with a 50% aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract is dried over sodium carbonate and concentrated. The concentrate is purified by silica gel column chromatography (eluent; n-hexane/ethyl acetate=1/0-10/1) and recrystallized from ethanol/n-hexane to give 1-(1-benzoyl-4-piperidinyl)-3,4-dihydrocarbostyril (35 g) as white powders, m.p. 108°-111° C.

Workup

  1. temperaturethe mixture is refluxed for 5 hours
  2. temperatureAfter cooling
  3. extractionthe reaction mixture is extracted with diethyl ether
  4. extractionextracted with ethyl acetate
  5. dry with materialThe extract is dried over sodium carbonate
  6. concentrationconcentrated
  7. customThe concentrate is purified by silica gel column chromatography (eluent; n-hexane/ethyl acetate=1/0-10/1)
  8. customrecrystallized from ethanol/n-hexane

Sources & evidence

ORD record
ord-9e6eb5ce746043318269404fb6e03183
Source dataset
uspto-grants-1997_07
Patent number
US05652247

Reaction notes

Loading…