Reacción #1350595

ord-65c5ee7c7cf14fd28ac87b0307fa786b

Ecuación de reacción

ClCCCl
EDC
Cn1nnc2cc(C(=O)O)ccc21
1-methylbenzotriazole-5-carboxylic acid
Cn1nccc1O
1-methyl-5-hydroxypyrazole
CC#N
acetonitrile
Cn1nccc1OC(=O)c1ccc2c(c1)nnn2C
1-Methylpyrazol-5-yl 1-Methylbenzotriazole-5-carboxylate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe mixture was extracted with ethyl acetate
  2. 2
    LavadoThe organic phase was washed
  3. 3
    Otrodried
  4. 4
    Otrothe product was then purified by crystallization

Procedimiento

1.5 g of 1-methylbenzotriazole-5-carboxylic acid (8.5 mmol) and 0.87 g of 1-methyl-5-hydroxypyrazole (8.9 mmol) were dissolved in 70 ml of abs. acetonitrile and admixed with 1.62 g of EDC (8.5 mmol), 2 ml of triethylamine and a catalytic amount of DMAP. After the reaction had ended, the solution was poured into water and the mixture was extracted with ethyl acetate. The organic phase was washed and dried, and the product was then purified by crystallization. Yield: 0.77 g (35%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06541423B1uspto-grants-2003_04