HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 118045699, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 118046444 | HCID 118046444 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118045699 | HCID 118045699 | — |
Reaction Steps
To a solution of methyl 3-(5-aminopyrazin-2-yl)propanoate (25 mg, 0.138 mmol) in CH3CN (690 μL) was added NBS (24.56 mg, 0.138 mmol). The reaction mixture was stirred for 1 h at room temperature. After quenched with Na2S2O3 solution, the reaction mixture was stirred with NaHCO3 solution for 20 min and extracted with EtOAc. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude methyl 3-(5-amino-6-bromopyrazin-2-yl)propanoate was obtained (28%). LCMS (m/z): 260.2/262.2 (MH+), 0.54 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242996B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-95ad4d11390c4864b01c897044c5f487 |
| Source note | uspto-grants-2016_01 |