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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417106Generated: October 26, 2026

Di-tert-butyl azodicarboxylate → 4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethoxy}-3-fluoro-benzonitrile

https://huagongshe.com/reaction/417106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant3-Fluoro-4-hydroxybenzonitrileHCID 2782944—
Reactant2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethanolHCID 66619310—
Product4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethoxy}-3-fluoro-benzonitrileHCID 6661944589%

Reaction Steps

The title compound was prepared in analogy to Example 4, intermediate, from 2-[2-(4-chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethanol (Ex. 1, int. c) and 3-fluoro-4-hydroxybenzonitrile (commercially available) and replacing di-ethyl azodicarboxylate by di-tert-butyl azodicarboxylate. The resulting solid was purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane and ethyl acetate (100:0 to 50:50) to give the desired compound as a colorless foam (89%). MS (Turbo Spray): m/z=510.3 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088930B2
Source datasetuspto-grants-2012_01
ORD IDord-2f82a461d7864cc39f72b20396f83c0c
Source noteuspto-grants-2012_01