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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83928Generated: October 30, 2026

tert-Butanol → HCID 66740647, compound

https://huagongshe.com/reaction/83928

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDiisopropylethylamineHCID 81531—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3-chloro-4-(2-(5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-(4-fluorophenyl)-1H-imidazol-2-yl)ethyl)-5-fluorobenzoic acidHCID 66740317—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 66740647HCID 66740647—

Reaction Conditions

Temperature0 °C

Reaction Steps

To solution of 3-chloro-4-(2-(5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)ethyl)-5-fluorobenzoic acid (540 mg) in a mixture of toluene (5 mL) and tert-butanol (1.5 mL) cooled to 0° C. was added diphenyl phosphoryl azide (DPPA) (1.1 eq, 302 mg) followed by DIPEA (1.3 eq, 226 μL). During addition of base, the white slurry became a clear solution, which was heated at 80° C. After 16 h, complete conversion was observed by LC-MS. The reaction was diluted with EtOAc, washed with satd NaHCO3, dried (Na2SO4), concentrated and purified by chromatography (silica, EtOAc/Hex, 10-60%) to yield tert-butyl 3-chloro-4-(2-(5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)ethyl)-5-fluorophenylcarbamate (230 mg). MS (EI) m/z 616 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846739B2
Source datasetuspto-grants-2014_09
ORD IDord-959baa3de8fe47649c253106b00405e8
Source noteuspto-grants-2014_09