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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116705Generated: October 29, 2026

Toluene → 4-(5-Phenyl-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonane

https://huagongshe.com/reaction/2116705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,4-Diazabicyclo(3.2.2)nonaneHCID 398407—
Reactant2-Chloro-5-phenylbenzoxazoleHCID 14169818—
ReactantSodium t-butoxideHCID 23676156—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(5-Phenyl-benzooxazol-2-YL)-1,4-diaza-bicyclo[3.2.2]nonaneHCID 2249580742.3%

Reaction Steps

1,4-Diazabicyclo[3.2.2]nonane (504 mg, 4.0 mmol) was added to a mixture of 2-chloro-5-phenylbenzoxazole (919 mg, 4.0 mmol), sodium tert-butoxide (423 mg, 4.4 mmol) and toluene (4 mL) at RT. The mixture was stirred at RT for 16 h and water (10 mL) and ethyl acetate (10 mL) were added. The layers were partitioned and the aqueous layer was extracted with ethyl acetate (3×10 mL). The combined organic layers were dried (Na2SO4), filtered and concentrated and the residue was purified by chromatography (Biotage, 40S) eluting with 4% MeOH in CHCl3, with 20 drops of NH4OH per liter of eluent to afford 540 mg (42%) of the title compound as an oil: 1H NMR (CDCl3, 400 MHz) δ 7.60-7.56 (m, 3H), 7.42 (t, 2H, J=7.7 Hz), 7.33-7.20 (m, 3H), 4.51 (s, 1H), 3.92 (t, 2H, J=5.8 Hz), 3.17-2.97 (m, 6H), 2.20-2.07 (m, 2H), 1.84-1.75 (m, 2H), 13C NMR (CDCl3, 100 MHz) δ 162.2, 148.6, 144.3, 141.9, 137.9, 129.0, 127.5, 127.1, 119.8, 114.8, 108.8, 57.3, 50.4, 46.5, 44.4, 27.0; MS (Cl) m/z 320.1 (M+1) The hydrochloride salt was prepared by diluting the title compound in ethyl acetate and adding a 2.5 N HCl in ethyl acetate solution: mp>300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439236B2
Source datasetuspto-grants-2008_10
ORD IDord-4a5db8293fed43bba1215703f5b08025
Source noteuspto-grants-2008_10