Reacción #1142858

ord-aed3a1fb3989488aad20ba2114c93642

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Analogously to the process described under Example 6A/Step 1, 1.0 g (3.62 mmol) of the compound of Example 4A and 804 mg (3.98 mmol) of 1-bromo-3-nitrobenzene gave 1.26 g (87% of theory) of the title compound. In this case, chromatographic isolation of the product was by MPLC (mobile phase cyclohexane/ethyl acetate 1:2); subsequent trituration with diisopropyl ether was dispensed with.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09394309B2uspto-grants-2016_07