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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558173Generated: October 29, 2026

Diisopropylethylamine → N-Phenyl-5-(2-(pyridin-4-yl)methylthiophenyl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/558173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-Pyridinemethanethiol hydrochlorideHCID 23093873—
Reactant5-(2-bromophenyl)-N-phenyl-1,3,4-oxadiazol-2-amineHCID 59152539—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductN-Phenyl-5-(2-(pyridin-4-yl)methylthiophenyl)-1,3,4-oxadiazol-2-amineHCID 2499235571.3%

Reaction Steps

A vessel containing 5-(2-bromophenyl)-N-phenyl-1,3,4-oxadiazol-2-amine (220 mg, 0.70 mmol; Reference Compound 7-(1)), tris(dibenzylideneacetone)dipalladium (33 mg, 0.035 mmol) and Xantphos (81 mg, 0.14 mmol) was replaced with nitrogen gas. To the vessel were added dioxane (5.0 mL), diisopropylethylamine (0.43 mL, 2.5 mmol) and 4-pyridinemethanethiol hydrochloride (210 mg, 1.3 mmol) successively at room temperature, and then the mixture was refluxed overnight. The reaction solution was cooled to room temperature and diluted with ethyl acetate (15 mL). The ethyl acetate solution was washed with a saturated brine solution (20 mL), dried over anhydrous sodium sulfate and concentrated under a reduced pressure. To the residue was added ethanol and a precipitated solid was filtered off and dried to give 180 mg (70%) of the titled compound as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063034B2
Source datasetuspto-grants-2011_11
ORD IDord-1f530c11d8ee4bd39eb35f4b5b3796c3
Source noteuspto-grants-2011_11