Реакция #156984

ord-89e62062841d41d2a7281f88b9107064

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The desired compound was prepared according to the procedure of Example 13, step A, using N-hydroxy-4-[(2-methoxyethyl)amino]-1,2,5-oxadiazole-3-carboximidoyl chloride [made according to Example 1, steps A through E] and 5-amino-2-fluorobenzonitrile [Aldrich, product #639877] as the starting materials in 100% yield. LCMS for C13H14FN6O3 (M+H)+: m/z=321.0.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822511B2uspto-grants-2014_09