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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038151Generated: October 30, 2026

2-(5-Nitro-1-trityl-1H-indazol-3-yl)-furo[3,2-c]pyridine → 2-(5-amino-1-trityl-1H-indazol-3-yl)-furo[3,2-c]pyridine

https://huagongshe.com/reaction/1038151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-Nitro-1-trityl-1H-indazol-3-yl)-furo[3,2-c]pyridineHCID 57686175—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-(5-amino-1-trityl-1H-indazol-3-yl)-furo[3,2-c]pyridineHCID 5768566180%

Reaction Steps

In a round-bottom flask equipped with a balloon, a mixture 2-(5-Nitro-1-trityl-1H-indazol-3-yl)-furo[3,2-c]pyridine (210 mg, 0.4 mmol) and 5% Pd on carbon (21 mg) in ethyl acetate and methanol (10 mL, 1:1) was hydrogenated overnight at room temperature to give 157 mg desired product (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-8aa526805e264a6888090ca3b7f0d6ec
Source noteuspto-grants-2013_10