Reacción #2083

ord-d7d7141538f0422c85b05b45f2b6979e

Ecuación de reacción

Cn1c(=O)[nH]c(=O)c2[nH]cnc21
3-methylxanthine
CCOCOCC
formaldehyde diethyl acetal
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
CC(=O)[O-].[Na+]
sodium acetate
CCOCn1cnc2c1c(=O)[nH]c(=O)n2C
crude product
CCOCn1cnc2c1c(=O)[nH]c(=O)n2C
7-Ethoxymethyl-3-methylxanthine

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwere introduced
  2. 2
    Temperaturaice-cooling
  3. 3
    workup.STIRRINGThe mixture was subsequently stirred for one hour
  4. 4
    workup.STIRRINGagain subsequently stirred for one hour
  5. 5
    TemperaturaAfter cooling to 10° C.
  6. 6
    Filtraciónthe precipitated product was filtered off with suction
  7. 7
    Lavadowashed with a little dimethylformamide
  8. 8
    Lavadowashed with demineralized water until chloride-free

Procedimiento

52.5 g (0.28 mol) of p-toluenesulfonyl chloride were initially introduced into 50 ml of dimethylformamide and 22.6 g (0.29 mol) of sodium acetate were introduced with stirring and ice-cooling. The mixture was subsequently stirred for one hour, treated with 39.1 g of formaldehyde diethyl acetal and again subsequently stirred for one hour. 41.5 g of 3-methylxanthine were then introduced and the reaction mixture was heated at 90° C. for 2 hours. After cooling to 10° C., the precipitated product was filtered off with suction, washed with a little dimethylformamide and washed with demineralized water until chloride-free. The crude product obtained was recrystallized from dimethylformamide.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728686uspto-grants-1998_03