HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595857Generated: October 31, 2026
N-bromobutanimide → HCID 123354204, compound
https://huagongshe.com/reaction/595857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 125487788 | HCID 125487788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 123354204 | HCID 123354204 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242996B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-a1473c1b87e34b2d94695eebde2afe1c |
|---|
| Source note | uspto-grants-2016_01 |
|---|