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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347844Generated: October 31, 2026

2-(Methylsulfanyl)-3-nitropyrazolo(1,5-a)pyridine → HCID 19010267, compound

https://huagongshe.com/reaction/347844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylsulfanyl)-3-nitropyrazolo(1,5-a)pyridineHCID 12371636—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 19010267HCID 19010267—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 2-methylthio-3-nitropyrazolo[1,5-a]pyridine (Reference; Heterocycles, 1977, 6, 379) (400 mg) in ethanol (20 mL), water (10 mL), acetic acid (2 mL) was added zinc powder (800 mg) and the reaction mixture was heated and stirred for 30 minutes at 80° C. The insoluble residue was filtered out, water was added to the filtrate and extraction was performed with ethyl acetate, and then the organic extract was washed with saturated aqueous sodium bicarbonate and brine. The organic extract was dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure to afford (2-methylthiopyrazolo[1,5-a]pyridin-3-yl)amine as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176216B2
Source datasetuspto-grants-2007_02
ORD IDord-5f4df3e09dba4de392d8c6dc7a35080b
Source noteuspto-grants-2007_02