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

HRID 2209543

반응식

HRID 2209543 반응식
[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

참가 물질

7

반응물 4

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

생성물 1

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

시약·촉매·용매 2

HCID 180Acetone용매HCID 702Ethanol용매2회

반응 조건

온도
50 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-deda93e3d2f94b4facad0997089cfcc9
출처 데이터셋
uspto-grants-1995_10
특허 번호
US05455253

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