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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-(Bromomethyl)quinoxaline | HCID 10214510 | — |
| Reactant | 2-(4-Tert-butylphenyl)-7-piperazin-1-yl-1,3-benzooxazole | HCID 57678312 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-({4-[2-(4-Tert-butylphenyl)-1,3-benzoxazol-7-yl]piperazin-1-yl}methyl)quinoxaline | HCID 11998144 | 69.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531542B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-3a28d413b5b640c6b3e4dd4a6bd5d140 |
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| Source note | uspto-grants-2009_05 |
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