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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634287Generated: November 1, 2026

Sodium Hydroxide → 5-Hydrazino-2-pyridinesulfonamide hydrochloride

https://huagongshe.com/reaction/1634287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
Reactant5-Aminopyridine-2-sulfonamideHCID 22313850—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Hydrazino-2-pyridinesulfonamide hydrochlorideHCID 2231382964.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-Sulfamyl-5-amino-pyridine (3 g) in concentrated hydrochloric acid solution (23 ml) was added NaNO2 (1.4 g, 20 mmol) in water (23 ml) while maintaining the temperature between −5° C. and 0° C. After the reaction mixture was stirred at 0° C. for 1.5 hours, SnCl2 (19 g) in concentrated hydrochloric acid solution (25 ml) was added, and the resulting reaction mixture was stirred at 0° C. for 1 hour, then room temperature overnight. The pH of the reaction solution was adjusted to 8 by addition of NaOH (24 g) in water (30 ml), followed by the addition of THF (200 ml). After stirred at room temperature for 30 minutes, the reaction mixture was filtered through Celite®. The aqueous layer was extracted with THF (3×200 ml) and ethyl acetate (2×200 ml). The combined organic layers were dried with sodium sulfate (Na2SO4), and concentrated in vacuo. The product was dissolved in 10% HCl in methanol (50 ml), and the solvent was removed in vacuo to give title compound (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506779B1
Source datasetuspto-grants-2003_01
ORD IDord-b22e3c5622bb45ab848e751b434ff559
Source noteuspto-grants-2003_01