HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486950Generated: October 30, 2026
N-bromobutanimide → 5-Bromo-6-fluoropyridin-2-amine
https://huagongshe.com/reaction/1486950
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Fluoropyridin-2-amine | HCID 2761399 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-6-fluoropyridin-2-amine | HCID 53418436 | 98% |
Reaction Steps
NBS (50.0 g, 280.99 mmol) was added slowly to 6-fluoropyridin-2-amine (30 g, 267.61 mmol) in MeCN (300 mL) cooled to 10-20° C. over a period of 30 minutes. The resulting solution was stirred at ambient temperature for 60 minutes then the solvent removed under reduced pressure. The residue was diluted with water, the precipitate collected by filtration, washed with water (200 mL) and dried under vacuum to afford the desired material (50.0 g, 98%) as a white solid, which was used without further purification. NMR Spectrum: 1H NMR (300 MHz, DMSO-d6) δ 6.29 (1H, d), 6.57 (2H, bs), 7.65 (1H, t). Mass Spectrum: m/z (ES+)[M+H]+=191.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428503B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6cbf6d159c9a4b61ae3bff8b3b1b584b |
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| Source note | uspto-grants-2016_08 |
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