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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491429Generated: October 26, 2026

Diisopropylethylamine → 6-({4-[2-(4-Tert-butylphenyl)-1,3-benzoxazol-7-yl]piperazin-1-yl}methyl)quinoxaline

https://huagongshe.com/reaction/491429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(Bromomethyl)quinoxalineHCID 10214510—
Reactant2-(4-Tert-butylphenyl)-7-piperazin-1-yl-1,3-benzooxazoleHCID 57678312—
SolventAcetonitrileHCID 6342—
Product6-({4-[2-(4-Tert-butylphenyl)-1,3-benzoxazol-7-yl]piperazin-1-yl}methyl)quinoxalineHCID 1199814469.4%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a suspension of 2-(4-tert-butylphenyl)-7-piperazin-1-yl-1,3-benzooxazole 23.5 mg, 0.070 mmol) and 6-bromomethylquinoxaline (17.2 mg, 0.077 mmol) in CH3CN (anh., 10 mL) was added ethyldiisopropylamine (0.015 mL, 0.084 mmol). The mixture was heated in a 95° C. bath overnight. The reaction was cooled to room temperature and concentrated in vacuo. The residue was adsorbed onto silica gel. Silica gel chromatography using a gradient of 25% EtOAc/hexane to 50% EtOAc/hexane then 100% EtOAc afforded the title compound (23.2 mg) as an ivory powder. MS (ESI) m/z 478 [M+H]+; HPLC Method C, r.t.=10.9 min (98.9% @210-370 nm; 97.4% @ 236 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531542B2
Source datasetuspto-grants-2009_05
ORD IDord-3a28d413b5b640c6b3e4dd4a6bd5d140
Source noteuspto-grants-2009_05