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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229392Generated: October 29, 2026

m-Anisoyl chloride → 7-Bromo-4-tert-butyl-5-(3-methoxybenzoyl)-4,5-dihydropyrrolo[1,2-a]quinoxaline

https://huagongshe.com/reaction/229392

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Anisoyl chlorideHCID 74374—
Reactant7-Bromo-4-tert-butyl-4,5-dihydropyrrolo[1,2-a]quinoxalineHCID 69062691—
Product7-Bromo-4-tert-butyl-5-(3-methoxybenzoyl)-4,5-dihydropyrrolo[1,2-a]quinoxalineHCID 69063614—

Reaction Steps

7-Bromo-4-tert-butyl-5-(3-methoxybenzoyl)-4,5-dihydropyrrolo[1,2-a]quinoxaline was prepared from 7-bromo-4-tert-butyl-4,5-dihydropyrrolo[1,2-a]quinoxaline and m-anisoyl chloride according to the procedure of Example 106, Step 2. The product was purified via Biotage Horizon® (25S, silica, gradient from 5% EtOAc/hexane to 40% EtOAc/hexane) and isolated as a white foam. MS (ESI) m/z 439/441 ([M+H]+); HRMS: calcd for C23H23BrN2O2, 438.0943; found (ESI+), 439.10084.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563793B2
Source datasetuspto-grants-2009_07
ORD IDord-be184283c48241a29f84db5e9bec6beb
Source noteuspto-grants-2009_07