反应 #3279157
相关文献 (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US07001917B2
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate (step 1 of Example 22) and 2-chloro-4-fluorobenzenesulfonamide: 1H-NMR (CDCl3) δ 8.12-8.07 (1H, m), 7.46-7.04 (11H, m), 6.29 (1H, br.s), 3.42-3.36 (2H, m), 2.79-2.75 (2H, m), 2.29 (3H, s), 2.21 (3H, s).
来源 ID: ord-60613f56e8f54bbf896aa59d6ed8a186