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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233670Generated: October 31, 2026

Diisopropylethylamine → 2-Pyridyl-pyrrolidin-1-yl-benzoxazole

https://huagongshe.com/reaction/233670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,5-DichlorobenzooxazoleHCID 10397578—
ReactantDichloromethane methanolHCID 21226129—
Reactant3-(4-Fluorophenyl)-2-(2-pyridyl)-pyrrolidineHCID 23356879—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-Pyridyl-pyrrolidin-1-yl-benzoxazoleHCID 86750192—

Reaction Steps

The crude pyrrolidine (5.9 g, 0.025M) was dissolved in 100 mL 1,4-dioxane containing N,N-diisopropylethylamine (435 mL, 0.025M). Then 2,5-dichlorobenzoxazole (4.7 g, 0.025M) was added and the resulting yellow solution was heated at reflux for 2 hours, cooled to room temperature and diluted with 250 mL ethyl acetate. The reaction mixture was washed with 200 mL portions of water and saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to obtain a yellow oil. Chromatography on silica gel with methylene chloride-methanol resulted in 4.6 g (47%) of the desired cis-+/--5-chloro-3-(4-fluorophenyl)-2-(2-pyridyl-pyrrolidin- 1-yl-benzoxazole, mp 149°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594008
Source datasetuspto-grants-1997_01
ORD IDord-d66a00aa640d45e9a2356da1dd1bb551
Source noteuspto-grants-1997_01