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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372465Generated: October 31, 2026

Hydrazine → 2-Hydrazinyl-5-iodopyridine

https://huagongshe.com/reaction/1372465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant2-Chloro-5-iodopyridineHCID 4397176—
SolventPyridineHCID 1049—
Product2-Hydrazinyl-5-iodopyridineHCID 22397188—

Reaction Steps

A mixture of 2-chloro-5-iodopyridine (1.918 g, 8.01 mmol), anhydrous hydrazine (1.26 mL, 40.05 mmol) and pyridine (30 mL) was warmed at reflux for 18 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was partitioned between dichloromethane and 1N aqueous sodium hydroxide solution. The organic layer was separated, dried (magnesium sulfate) and concentrated under reduced pressure. The residue was triturated with hexanes, and the resultant precipitate was collected and dried in vacuo to afford the title compound as off-white crystals. LC/MS 235.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157490B2
Source datasetuspto-grants-2007_01
ORD IDord-bea3ef6a301e4f3685fe133979457d6b
Source noteuspto-grants-2007_01