Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624456Generated: October 27, 2026

Triethylamine → [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-(5-phenyl-[1,3,4]oxadiazol-2-yl)-amine

https://huagongshe.com/reaction/1624456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoylhydrazineHCID 11955—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-(4-Bromophenyl)-3-methyl-1,2-oxazole-4-carboxylic acidHCID 56604559—
ReactantHCID 178479711HCID 178479711—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-(5-phenyl-[1,3,4]oxadiazol-2-yl)-amineHCID 66577739—

Reaction Conditions

Temperature60 °C

Reaction Steps

5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid (1 g, 3.6 mmol), triethylamine (1 mL, 7.2 mmol) and diphenylphosphoryl azide (1.98 g, 7.2 mmol) were placed in toluene (20 mL) and heated to 60° C. for 20 minutes. Benzoic acid hydrazide (0.98 g, 7.2 mmol) was added in a single portion and the reaction was heated and stirred for 2 hours. The reaction was cooled and submitted to aqueous workup. The crude material was dissolved in dioxane (100 mL), phosphorous(V) oxychloride was added and the reaction was heated to 100° C. overnight. The reaction was cooled and worked up and the residue was purified on silica gel (0-80% EtOAc in hexanes) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778983B2
Source datasetuspto-grants-2014_07
ORD IDord-77338a2231db4cb4b8be69ade6b54f22
Source noteuspto-grants-2014_07