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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409388Generated: October 31, 2026

2-Amino-5-bromopyridine → HCID 178526354, compound

https://huagongshe.com/reaction/2409388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventIsopropanolHCID 3776—
ProductHCID 178526354HCID 17852635475.3%

Reaction Conditions

Temperature50 °C

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 3H 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815894B2
Source datasetuspto-grants-2014_08
ORD IDord-09e73350d3e54e55bbb78e56dc4df27c
Source noteuspto-grants-2014_08