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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732477Generated: November 1, 2026

3-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridine → HCID 53813641, compound

https://huagongshe.com/reaction/1732477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridineHCID 54128243—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53813641HCID 53813641—

Reaction Steps

A solution of 0.542 gm. (0.002 mole) of 3-nitro-6-phenylthioimidazo [1,2-a] pyridine in 20 ml. of dioxane is reduced at 40 psi. under a hydrogen atmosphere with 0.500 g. of 5% palladium on carbon as catalyst. When the uptake of hydrogen is complete, the catalyst is removed by filtration. The filtrate is evaporated in vacuo to yield 3-amino-6-phenylthioimidazo [1,2-a] pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237300
Source datasetuspto-grants-1980_12
ORD IDord-c4c0ffac28b4472aabeb70231a6e7b4a
Source noteuspto-grants-1980_12