Reacción #61540
ord-10dda125a7034fc9b1c612e1464b988d
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroquenched with diluted HCl
- 2Filtraciónfiltered through a chem elut® cartridge by elution with ethyl acetate and DCM
- 3ConcentraciónAfter concentration under reduced pressure the crude residue
- 4Otrowas directly subjected to the next reaction step
Procedimiento
To a solution of 1 g 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-1H-pyrazole-3,5-dicarboxylic acid 3-ethyl ester in 15 ml THF 314 mg LiBH4 were added cautiously. Then the reaction mixture was stirred for 16 h, quenched with diluted HCl and filtered through a chem elut® cartridge by elution with ethyl acetate and DCM. After concentration under reduced pressure the crude residue was directly subjected to the next reaction step. Yield: 800 mg.