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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595857Generated: October 31, 2026

N-bromobutanimide → HCID 123354204, compound

https://huagongshe.com/reaction/595857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 125487788HCID 125487788—
SolventAcetonitrileHCID 6342—
ProductHCID 123354204HCID 123354204—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-((1R,3S)-3-((tert-butyldimethylsilyl)oxy)cyclohexyl)pyrazin-2-amine (110 mg, 0.358 mmol) in acetonitrile (5.50 mL) was added NBS (66.9 mg, 0.376 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 15 min. After quenched with sat sodium thiosulfate and sat NaHCO3, extracted with EtOAc three times. The organic layers were combined and washed with brine, dried over Na2SO4, filtered and concentrated to afford 138 mg of desired cis racemate compound, which was used as it was. LCMS (m/z): 388 (MH+), 0.72 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-a1473c1b87e34b2d94695eebde2afe1c
Source noteuspto-grants-2016_01