HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595849Generated: October 26, 2026
N-bromobutanimide → 5-Bromo-4-fluoropyridin-2-amine
https://huagongshe.com/reaction/595849
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-4-fluoropyridine | HCID 18327808 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-4-fluoropyridin-2-amine | HCID 57917407 | — |
Reaction Steps
To a solution of 4-fluoropyridin-2-amine (400 mg, 3.57 mmol) in acetonitrile (35. 7 mL) was added NBS (648 mg, 3.64 mmol) in three portions at 0° C. The reaction mixture was stirred at 0° C. for 20 min. LCMS showed the reaction complete. After quenched with sat Na2S2O3 and NaHCO3, stirred for 30 min. The reaction mixture was extracted with EtOAc 3 times. Washed by sat NaHCO3, water and brine. Dried and concentrated. The crude material was triturated with ether and taken to the next step without further purification. LCMS (m/z): 192.9 (MH+), 0.32 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-b72c715eb5734b23879523d7ca3a1739 |
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| Source note | uspto-grants-2016_01 |
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