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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589050Generated: October 30, 2026

Acetic Acid → HCID 90410414, compound

https://huagongshe.com/reaction/589050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 90409483HCID 90409483—
SolventEthyl AcetateHCID 8857—
ProductHCID 90410414HCID 9041041485%

Reaction Steps

The 4-piperidin-2-yl-4,5-dihydroimidazo[1,5,4-de][1,4]benzoxazin-2(1H)-one (0.20 g, 0.77 mmol) of Step 1 was dissolved in acetic acid (10.0 mL, 176 mmol) at room temperature and N-bromosuccinimide (0.14 g, 0.77 mmol) was slowly added. The reaction was stirred for 2 h and was concentrated in vacuo to give a residue. The residue was dissolved in ethyl acetate, washed with aqueous potassium carbonate, washed with brine, dried over magnesium sulfate, and concentrated to give 7-bromo-4-piperidin-2-yl-4,5-dihydroimidazo[1,5,4-de][1,4]benzoxazin-2(1H)-one as a dark oil (0.22 g, 85%). LCMS calculated for C14H17BrN3O2 (M+H)+: m/z=338.0, 340.0. found: 338.0, 340.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227985B2
Source datasetuspto-grants-2016_01
ORD IDord-36c9085b930b4ec999f32fc9767353e2
Source noteuspto-grants-2016_01