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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873920Generated: October 31, 2026

3,8-Dimethyl-6-nitro-[1,2,4]triazolo[4,3-A]pyridine → 3,8-Dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-amine

https://huagongshe.com/reaction/873920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,8-Dimethyl-6-nitro-[1,2,4]triazolo[4,3-A]pyridineHCID 74889142—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3,8-Dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-amineHCID 75357449—

Reaction Steps

A suspension of 3,8-dimethyl-6-nitro-[1,2,4]triazolo[4,3-a]pyridine (Step 67.3) (14.1 g, 71.9 mmol) and 10% Pd/C (2.75 g, 25.9 mmol) in MeOH (300 mL) was shaken for 5 h under 4 bar hydrogen atmosphere at RT. Further 10% Pd/C was added and the reaction mixture was shaken another 1 hh under hydrogen atmosphere. The mixture was filtered through Celite. The pad of Celite was washed with MeOH and the resulting filtrate was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane/(CH2Cl2-MeOH 19:1) 50-100% (CH2Cl2-MeOH 19:1)) to afford the title product as yellow solid. tR: 0.29 min (LC-MS 2); ESI-MS: 163 [M+H]+ (LC-MS 2); TLC (CH2Cl2-MeOH 9:1) Rf=0.26; 1H NMR (400 MHz, DMSO-d6) δ ppm 2.43 (s, 3H) 2.54 (s, 3H) 5.05 (br. s, 2H) 6.75 (br. s, 1H) 7.18 (br. s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975417B2
Source datasetuspto-grants-2015_03
ORD IDord-7ab2eb257cf4424ea04967591e94b48c
Source noteuspto-grants-2015_03