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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502168Generated: October 31, 2026

5-nitro-2-(1H-tetrazol-1-yl)pyridine → 6-(1H-1,2,3,4-tetrazol-1-yl)pyridin-3-amine

https://huagongshe.com/reaction/1502168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-nitro-2-(1H-tetrazol-1-yl)pyridineHCID 66927291—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product6-(1H-1,2,3,4-tetrazol-1-yl)pyridin-3-amineHCID 66927338—

Reaction Conditions

Temperature50 °C

Reaction Steps

5-Nitro-2-(1H-tetrazol-1-yl)pyridine (1020 mg, 5.31 mmol) was suspended in acetic acid (10 ml). Zinc (3472 mg, 53.1 mmol) was added slowly (exothermic reaction). The mixture was stirred at 50° C. for 1 hour, cooled, diluted with EtOAc. The mixture was filtered, rinsed with ethyl acetate. The filtrate was concentrated to dryness to give crude 6-(1H-tetrazol-1-yl)pyridin-3-amine: LC/MS: [(M+1-28)]+=135.1.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-54587d0a04e94856ae4a725733cffb33
Source noteuspto-grants-2015_12