1,3-Cyclohexanedione → 2-Methyl-4-(3-chloro-4-fluorophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone

HRID 2209543

Reaction equation

HRID 2209543 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[CH:5]=O.[C:11]1(=[O:18])[CH2:16][CH2:15][CH2:14][C:13](=O)[CH2:12]1.[C:19]([O-])(=O)C.[NH4+].C(O)(=O)C.[NH:28]1[CH2:32][CH2:31]CC1>C(O)C.CC(C)=O>[CH3:19][C:32]1[NH:28][C:13]2[CH2:14][CH2:15][CH2:16][C:11](=[O:18])[C:12]=2[CH:5]([C:4]2[CH:7]=[CH:8][C:9]([F:10])=[C:2]([Cl:1])[CH:3]=2)[CH:31]=1

Participants

7

Reactant 4

HCID 104341,3-CyclohexanedioneHCID 517165Ammonium AcetateHCID 5938663-Chloro-4-fluorobenzaldehydeHCID 11040738Pyrrolidine, acetate

Product 1

HCID 199589372-Methyl-4-(3-chloro-4-fluorophenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneYield 2.8%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 702EthanolSolvent2×

Conditions

Temperature
50 °C

Procedure

A mixture of 3-chloro-4-fluoro benzaldehyde (2.7 g), 1,3-cyclohexanedione (1.99 g) and 47 mL of ethanol were heated at 50° C. overnight and then cooled to room temperature. Acetone (1.18 g), ammonium acetate (1.97 g) and a premixed solution of pyrrolidine acetate (20.4 mmole) in 5 mL of ethanol were added and heated at 70° C. for three hours and then cooled to room temperature. The solvent was evaporated in vacuo and the residue was partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Chromatography (eluant: ether/hexane; 9.0/1.0) over silica gel provided the title compound 0.140 g as a yellow solid, m.p. 164°-167° C. 1H-NMR (300 MHz, d6-DMSO): 1.74(s, 3H,CH3), 1.81-1.88(m, 2H, CH2) 2.15-2.19(m,2H, CH2), 2.41-2.48(m,2H,CH2), 4.41(d,1H, J=4.8 Hz, CH), 4.60(d, 1H, J=4.8(Hz,CH), 7.10-7.28(m,3H, aromatic), 8.54(s, 1H, NH); MS (Cl, CH4): 292 (M+1): Analysis for C16H15ClFNO: Calculated: C; 65.87; H; 5.18; N; 4.80: Found: C; 65.67; H; 5.50; N; 4.48.

Workup

  1. temperaturecooled to room temperature
  2. temperatureheated at 70° C. for three hours
  3. temperaturecooled to room temperature
  4. customThe solvent was evaporated in vacuo
  5. customthe residue was partitioned between water and ethyl acetate
  6. dry with materialThe organic layer was dried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-deda93e3d2f94b4facad0997089cfcc9
Source dataset
uspto-grants-1995_10
Patent number
US05455253

Linked notes

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