Réaction #792164
ord-0461b837d19145d68403bd3719bf0eba
Équation de réaction
benzoxazinone
6-Chloro-2-[3-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazin-4-one
isopropylamine
tetrahydrofuran
→
title compound
3-chloro-N-[4-chloro-2-methyl-6-[[(1-methylethyl)amino]-carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
Réactifs
Réactifs
Aucun
Conditions de réaction
Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températurecooled to room temperature
- 2AutreThe tetrahydrofuran solvent was evaporated under reduced pressure
- 3Autrethe residual solid was purified by chromatography on silica gel
Mode opératoire
To a solution of the benzoxazinone product of Step E (6.21 g, 15.21 mmol) in tetrahydrofuran (100 mL) was added isopropylamine (4.23 g, 72.74 mmol) and the reaction mixture was then heated to 60° C., stirred for 1 hour and then cooled to room temperature. The tetrahydrofuran solvent was evaporated under reduced pressure, and the residual solid was purified by chromatography on silica gel to afford the title compound, a compound of the present invention, as a white solid (5.05 g) melting at 173-175° C.