Reaktion #49977

ord-df276dfc5b8f41f39fbda1b70b2c26ca

Reaktionsgleichung

CC(=O)CC(C)=O
2,4-pentanedione
CCOC(=O)C=C(N)OCC.Cl
ethyl 3-amino-3-ethoxyacrylate hydrochloride
COc1ccc(CN)cc1
4-methoxybenzylamine
CCOC(=O)c1c(C)cc(C)nc1NCc1ccc(OC)cc1
ethyl 2-(4-methoxybenzylamino )-4,6-dimethylnicotinate
[K+].[OH-]
potassium hydroxide
COc1ccc(CNc2nc(C)cc(C)c2C(N)=O)cc1
product
Ausbeute 70.0%
COc1ccc(CNc2nc(C)cc(C)c2C(N)=O)cc1
2-(4-methoxybenzylamino)-4,6-dimethylnicotinamide
Ausbeute 70.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
22°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was heated to 80° C. for 3 h
  2. 2
    TemperaturThe reaction is cooled to 22° C.
  3. 3
    workup.WAITThe reaction mixture is aged at room temperature for 24 hours
  4. 4
    SonstigeDuring the age the nicotinate precipitates out of the reaction
  5. 5
    EinengenThe reaction mixture is concentrated in vacuo
  6. 6
    SonstigeThe crude mixture is chromatographed on silica gel

Vorschrift

In a three-necked flask containing ethanol (6.12mL) is added ethyl 3-amino-3-ethoxyacrylate hydrochloride(3g, 15.3mmol). The solution is treated with 4-methoxybenzylamine(2mL, 15.3mmol) and the mixture is stirred at 22° C. for 1.5 h. The reaction mixture was heated to 80° C. for 3 h. The reaction is cooled to 22° C. and an ethanolic solution of potassium hydroxide (0.86 g, 15.3 mmol, 25.0 mL of ethanol) is added. Neat 2,4-pentanedione (1.57 mL, 15.3 mmol) is added to the solution dropwise over 15 minutes at room temperature. The reaction mixture is aged at room temperature for 24 hours. During the age the nicotinate precipitates out of the reaction as does KCl. The reaction mixture is concentrated in vacuo. The crude mixture is chromatographed on silica gel to afford a 70% yield of the product, ethyl 2-(4-methoxybenzylamino )-4,6-dimethylnicotinate, 27.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05424432uspto-grants-1995_06