HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576129Generated: October 29, 2026
2-Amino-5-bromopyridine → HCID 178526354, compound
https://huagongshe.com/reaction/576129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178526354 | HCID 178526354 | 75.3% |
Reaction Steps
To a 1 L round-bottom flask was added 2-amino-5-bromopyridine (100 g, 578 mmol), DMF-DMA (101 mL, 751 mmol) and 2-propanol (200 mL). The mixture was heated to reflux for 3 h to give a clear dark solution. It was then cooled to 50° C. and hydroxylamine hydrochloride (52.2 g, 751 mmol) was added. The mixture was stirred at 50° C. overnight to give a yellow suspension. The precipitate was collected by filtration. The black filtrate was concentrated and the residue was stirred in EtOH (20 mL) for 20 min. The solid was collected by filtration. The combined solids were dried in an oven to give N-(5-bromopyridin-2-yl)-N′-hydroxyformimidamide as a sandy solid (94 g, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034899B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-a36af77543b34bee96324ba51657c65c |
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| Source note | uspto-grants-2015_05 |
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