Methanol → Ethyl 3-(4-chlorophenyl)-2-(4-((dimethylamino)methyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate

HRID 908001Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 908001
[CH3:1][N:2]([CH2:4][C:5]1[CH:22]=[CH:21][C:8](/[CH:9]=[N:10]/[C:11]2[CH:19]=[CH:18]C=C3[C:12]=2[CH2:13][O:14]C3=O)=[CH:7][CH:6]=1)[CH3:3].[Cl:23][C:24]1[CH:31]=[CH:30][C:27]([CH:28]=O)=[CH:26][CH:25]=1.C[O-].[Na+].CO.[C:37]([O:41][CH2:42][CH3:43])(=[O:40])[CH2:38][CH3:39]>>[Cl:23][C:24]1[CH:31]=[CH:30][C:27]([CH:28]2[C:13](=[O:14])[C:12]3[C:38]([C:37]([O:41][CH2:42][CH3:43])=[O:40])=[CH:39][CH:18]=[CH:19][C:11]=3[NH:10][CH:9]2[C:8]2[CH:7]=[CH:6][C:5]([CH2:4][N:2]([CH3:3])[CH3:1])=[CH:22][CH:21]=2)=[CH:26][CH:25]=1

Komponenten

6

Edukt 5

HCID 887MethanolHCID 77264-ChlorobenzaldehydeHCID 7749Ethyl PropionateHCID 10942334Sodium MethoxideHCID 178483208HCID 178483208, Verbindung

Produkt 1

HCID 67258647Ethyl 3-(4-chlorophenyl)-2-(4-((dimethylamino)methyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylateAusbeute 28 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A mixture of (E)-4-(4-((dimethylamino)methyl)benzylideneamino)isobenzofuran-1(3H)-one (588 mg, 2 mmol) and 4-chlorobenzaldehyde (281 mg, 2 mmol) in anhydrous ethyl propionate (25 mL) was cooled to 0° C. The sodium methoxide in methanol solution (sodium (115 mg, 5 mmol) in anhydrous ethanol (10 mL)) was added dropwise and the mixture was stirred at 25° C. for 3 hr. The resulting mixture was quenched with water (5 mL), and then evaporated under reduced pressure. The residue was extracted with ethyl acetate (100 mL×3) and the combined organic layers were dried over anhydrous sodium sulfate and concentrated to give crude product, which was purified by column chromatography (silica gel, dichloromethane to dichloromethane/methanol=30:1) to give the title compound (260 mg, yield 28%) as a yellow solid. LC-MS (ESI) m/z: 463 (M+1)+.

Aufarbeitung

  1. customThe resulting mixture was quenched with water (5 mL)
  2. customevaporated under reduced pressure
  3. extractionThe residue was extracted with ethyl acetate (100 mL×3)
  4. dry with materialthe combined organic layers were dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customto give crude product, which
  7. customwas purified by column chromatography (silica gel, dichloromethane to dichloromethane/methanol=30:1)

Quellen und Nachweise

ORD-Eintrag
ord-e23946b1e4ca46879e1b483da9491a91
Quelldatensatz
uspto-grants-2011_09
Patentnummer
US08012976B2

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