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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446738Generated: October 30, 2026

N-bromobutanimide → HCID 58293816, compound

https://huagongshe.com/reaction/446738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 58293789HCID 58293789—
SolventAcetonitrileHCID 6342—
ProductHCID 58293816HCID 5829381615.3%

Reaction Steps

Compound 1084 (200 mg, 0.54 mmol) was dissolved in 10 mL of acetonitrile. N-Bromosuccinimide (96 mg, 0.54 mmol) was added to the solution and the reaction mixture was stirred at room temperature for 30 minutes. The reaction was quenched with 1 M Na2S2O3 and the mixture extracted with ethyl acetate. The organice layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford a white solid that was purified by silica gel chromatography to afford 37 mg of N-tert-butyl-5-bromo-3-(1-(4-cyclopropyl-2,3-difluorophenyl)-1H-tetrazol-5-yl)pyridin-2-amine (Compound 1085); MS (M+1)=449.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481524B2
Source datasetuspto-grants-2013_07
ORD IDord-2086e50088704f8b99dc6a44e3180704
Source noteuspto-grants-2013_07