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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696476Generated: October 31, 2026

6-Aminoquinoline → 6-Hydrazinylquinoline hydrochloride

https://huagongshe.com/reaction/1696476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminoquinolineHCID 11373—
ReactantStannous ChlorideHCID 24479—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
Product6-Hydrazinylquinoline hydrochlorideHCID 5340868877%

Reaction Steps

To a solution of quinolin-6-ylamine (5 g, 35 mmol) in conc. HCl (12 mL) was added dropwise an aqueous solution (4 mL) of NaNO2 (2.42 g, 35 mmol) at 0° C. The resulting mixture was stirred for 1 h and then treated dropwise with a solution of SnCl2 2H2O (15.8 g, 70 mmol) in conc. HCl (15 mL) at 0° C. The reaction mixture was stirred for 2 h at RT. The precipitate was collected and washed with EtOH and Et2O to yield 1-(quinolin-6-yl)hydrazine hydrochloride as a yellow powder (4.3 g, 77% yield), which was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163756B2
Source datasetuspto-grants-2012_04
ORD IDord-d1191acf4035479f97501a460505b2a1
Source noteuspto-grants-2012_04