Reacción #216906

ord-09efa1ff6f7d48a08bf9697de6c52e06

Ecuación de reacción

O=Cc1ccncc1
Pyridine-4-carbaldehyde
N[C@@H](CS)C(=O)O
L-cysteine
C
charcoal
O=C(O)C1CSC(c2ccncc2)N1
2-(4-pyridyl)-thiazolidine-4-carboxylic acid
Rendimiento 57.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas warm
  2. 2
    FiltraciónThe mixture was filtered
  3. 3
    TemperaturaAfter cooling
  4. 4
    Filtraciónthe resultant crystalline precipitate was collected by filtration
  5. 5
    Lavadowashed with ethanol

Procedimiento

Pyridine-4-carbaldehyde (1.07 g) and 1.21 g of L-cysteine were heated in 60% ethanol at a refluxing temperature for 4 hours. Activated charcoal (100 mg) was added to the reaction mixture while it was warm. The mixture was filtered. After cooling, the resultant crystalline precipitate was collected by filtration and washed with ethanol to give 1.2 g of 2-(4-pyridyl)-thiazolidine-4-carboxylic acid. Melting point 171°-173° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05470851uspto-grants-1995_11