Reacción #1889452

ord-f79cb17bb4674bdf94f0b7ecde77a353

Ecuación de reacción

Cn1ncc(C(=O)Cl)c1C(=O)Nc1ccn2nc(-c3ccccc3)nc2c1
1-methyl-5-(2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1H-pyrazole-4-carbonyl chloride
CNCC(=O)OC.Cl
methyl 2-(methylamino)acetate hydrochloride
COC(=O)CN(C)C(=O)c1cnn(C)c1C(=O)Nc1ccn2nc(-c3ccccc3)nc2c1
final product
COC(=O)CN(C)C(=O)c1cnn(C)c1C(=O)Nc1ccn2nc(-c3ccccc3)nc2c1
{Methyl-[1-methyl-5-(2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1H-pyrazole-4-carbonyl]-amino}-acetic acid methyl ester

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThis compound was prepared in the same manner

Procedimiento

This compound was prepared in the same manner as described in example 92 starting from 1-methyl-5-(2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1H-pyrazole-4-carbonyl chloride (Example 92, step a) (263 mg, 691 μmol) and methyl 2-(methylamino)acetate hydrochloride (482 mg, 3.45 mmol). Additional TEA (349 mg, 481 μl) was added to the reaction mixture. The final product was isolated as white solid (146 mg, 46%); MS: m/z=448.2 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08349824B2uspto-grants-2013_01