HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004292Generated: October 29, 2026
2-Amino-5-bromopyridine → HCID 53812896, compound
https://huagongshe.com/reaction/1004292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 53827885 | HCID 53827885 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53812896 | HCID 53812896 | — |
Reaction Steps
A mixture of 28-4 (0.3 g, 1.0 mmol), 2-amino-5-bromopyridine (0.3 g, 1.9 mmol), KOAc (0.3 g, 2.4 mmol) and Pd(OAc)2 (0.02 g, 0.1 mmol) in 6 mL DMF was purged with argon for 5 min and then heated at 90° C. for 7 hr and 115° C. for 48 hr. It was cooled, treated with 50 mL water and extracted with EtOAc (×3). The combined organic layers were washed with brine and dried over Na2SO4. After solvent removal, the residue was purified using silica gel flash chromatography (100% EtOAc to EtOAc/MeOH 10:1) to afford the desired product 28-5 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048861 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-fe26211be2f441b8a0614e59ace1fc79 |
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| Source note | uspto-grants-2000_04 |
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