Reacción #2161251

ord-c4b9b8d57d234046a9bf3b6c3026b5f2

Ecuación de reacción

CCOC(=O)c1nc([N+](=O)[O-])cn1CC1CC1
ethyl 1-(cyclopropylmethyl)-4-nitro-1H-imidazole-2-carboxylate
[H][H]
hydrogen
CCOC(=O)c1nc(N)cn1CC1CC1
Ethyl 4-amino-1-(cyclopropylmethyl)-1H-imidazole-2-carboxylate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe catalyst is filtered off
  2. 2
    Concentraciónthe filtrate is concentrated in vacuo
  3. 3
    OtroThe concentration residue is directly used further for the next reaction

Procedimiento

3.89 g (16.26 mmol) of ethyl 1-(cyclopropylmethyl)-4-nitro-1H-imidazole-2-carboxylate are dissolved in 50 ml of THF, and a spatula tip of Raney nickel is added. In a hydrogenation apparatus, the reaction mixture is hydrogenated with hydrogen at room temperature. The catalyst is filtered off and the filtrate is concentrated in vacuo. The concentration residue is directly used further for the next reaction.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07919489B2uspto-grants-2011_04