HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595823Generated: October 31, 2026
N-bromobutanimide → HCID 118045604, compound
https://huagongshe.com/reaction/595823
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 118046480 | HCID 118046480 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118045604 | HCID 118045604 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ce5a4f43e79c4f9db6ba01a310b1af33 |
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| Source note | uspto-grants-2016_01 |
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