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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595823Generated: October 31, 2026

N-bromobutanimide → HCID 118045604, compound

https://huagongshe.com/reaction/595823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 118046480HCID 118046480—
SolventAcetonitrileHCID 6342—
ProductHCID 118045604HCID 11804560438%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(6-aminopyridin-3-yl)tetrahydrothiophene 1,1-dioxide (96 mg, 0.452 mmol) was dissolved in acetonitrile (5 mL) and the solution was cooled to 0° C., to it was added NBS (80 mg, 0.452 mmol) and the mixture was stirred at 0° C. for 40 min. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between EtOAc/sat. NaHCO3 (30 mL/20 mL), the EtOAc layer was washed with sat. Na2CO3 (20 mL), brine (20 mL), dried (Na2SO4), filtered off and concentrated in vacuo yielding 3-(6-amino-5-bromopyridin-3-yl)tetrahydrothiophene 1,1-dioxide as light brown oil (50 mg, 38% yield). LCMS (m/z): 293.0/291.0 (MH+), 0.29 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-ce5a4f43e79c4f9db6ba01a310b1af33
Source noteuspto-grants-2016_01