HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425911Generated: October 26, 2026
N-bromobutanimide → 5-Bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine
https://huagongshe.com/reaction/425911
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(2,6-Dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine | HCID 21111400 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine | HCID 21111485 | 51% |
Reaction Steps
5-bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine was prepared following procedure 1. A stirring solution of 3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine (9.07 g, 0.03 mol) in acetonitrile was cooled to 0° C. using an ice bath. To this solution was added NBS (5.33 g, 0.03 mol) portionwise. The reaction was stirred at 0° C. for 15 min. The reaction was concentrated to dryness under vacuum. The resulting dark oil was dissolved in EtOAc (500 mL), and purified via silica gel chromatography. The solvents were then removed in vacuo to yield 5-bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine (5.8 g, 0.015 mol, 51%) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106197B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e92353001d6d40ff81a529730b262d62 |
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| Source note | uspto-grants-2012_01 |
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