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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385737Generated: October 31, 2026

5-[6-(1-Hydroxy-1-methylethyl)pyridin-3-yl]-2-nitrothiophene-3-carboxamide → 2-Amino-5-[6-(1-hydroxy-1-methylethyl)pyridin-3-yl]thiophene-3-carboxamide

https://huagongshe.com/reaction/385737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[6-(1-Hydroxy-1-methylethyl)pyridin-3-yl]-2-nitrothiophene-3-carboxamideHCID 59525801—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product2-Amino-5-[6-(1-hydroxy-1-methylethyl)pyridin-3-yl]thiophene-3-carboxamideHCID 59526287—

Reaction Steps

To 5-[6-(1-hydroxy-1-methylethyl)pyridin-3-yl]-2-nitrothiophene-3-carboxamide (245 mg, 0.80 mmol) in MeOH (20 mL) was added 3% Pt/C doped with 0.6% V (52 mg, 8.0 μmol). The reaction was stirred under a hydrogen balloon at room temperature for 4 h. The solution was diluted with MeOH, filtered through Celite, and evaporated to give the title compound as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-aea4087658dc4ec3906237c71749853f
Source noteuspto-grants-2013_02