Reacción #586094

ord-8c089002d79140d496a88770b3a9da83

Ecuación de reacción

O
water
Cl.O=C1CN2CCC1CC2
3-Quinuclidinone hydrochloride
[K+].[OH-]
Potassium hydroxide
O=Cc1cccnc1
3-Pyridinecarboxaldehyde
O=C1C(=Cc2cccnc2)N2CCC1CC2
yellow solid
Rendimiento 76.2%
O=C1C(=Cc2cccnc2)N2CCC1CC2
2-((3-Pyridinyl)methylene)-1-azabicyclo[2.2.2]octan-3-one
Rendimiento 76.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture stirred for 16 h at ambient temperature
  2. 2
    workup.WAITThe reaction mixture became yellow during this period, with solids
  3. 3
    workup.DISSOLUTIONWhen the solids dissolved
  4. 4
    Temperaturathe mixture was cooled at 4° C. overnight
  5. 5
    FiltraciónThe crystals were collected by filtration
  6. 6
    Lavadowashed with water, and air
  7. 7
    Otrodried

Procedimiento

Potassium hydroxide (56 g, 0.54 mole) was dissolved in methanol (420 mL). 3-Quinuclidinone hydrochloride (75 g, 0.49 mole) was added and the mixture was stirred for 30 min at ambient temperature. 3-Pyridinecarboxaldehyde (58 g, 0.54 mole) was added and the mixture stirred for 16 h at ambient temperature. The reaction mixture became yellow during this period, with solids caking on the walls of the flask. The solids were scraped from the walls and the chunks broken up. With rapid stirring, water (390 mL) was added. When the solids dissolved, the mixture was cooled at 4° C. overnight. The crystals were collected by filtration, washed with water, and air dried to obtain 80 g of yellow solid. A second crop (8 g) was obtained by concentration of the filtrate to ˜10% of its former volume and cooling at 4° C. overnight. Both crops were sufficiently pure for further transformation (88 g, 82%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07767193B2uspto-grants-2010_08