Reacción #502106

ord-9738909b5b2b4a118505adb3bac6ad7f

Ecuación de reacción

O=C(O)c1n[nH]c2ccccc12
1H-indazole-3-carboxylic acid
CNOC.Cl
N,O-dimethylhydroxylamine hydrochloride
CCN=C=NCCCN(C)C
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
c1ccncc1
pyridine
CON(C)C(=O)c1n[nH]c2ccccc12
compound
Rendimiento 69.1%
CON(C)C(=O)c1n[nH]c2ccccc12
N-Methoxy-N-methyl-1H-indazole-3-carboxamide
Rendimiento 69.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe mixture is concentrated
  2. 2
    OtroThe yellow precipitate obtained
  3. 3
    Lavadois washed with water
  4. 4
    Otrodried under reduced pressure

Procedimiento

In a round-bottomed flask, 4.0 g of 1H-indazole-3-carboxylic acid, 2.6 g of N,O-dimethylhydroxylamine hydrochloride, 9.4 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide and 8.4 ml of pyridine are placed in 120 ml of tetrahydrofuran. The mixture is stirred at ambient temperature for 20 h. The mixture is concentrated and the residue is taken up in water. The yellow precipitate obtained is washed with water and then dried under reduced pressure. 3.5 g of compound are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088765B2uspto-grants-2012_01