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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038103Generated: October 31, 2026

Ethylamine → ethyl-[4-(5-nitro-1-trityl-1H-indazol-3-yl)-pyridin-2-yl]-amine

https://huagongshe.com/reaction/1038103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant3-(2-fluoro-pyridin-4-yl)-5-nitro-1-trityl-1H-indazoleHCID 58371921—
SolventTetrahydrofuranHCID 8028—
Productethyl-[4-(5-nitro-1-trityl-1H-indazol-3-yl)-pyridin-2-yl]-amineHCID 6741946236%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-(2-fluoro-pyridin-4-yl)-5-nitro-1-trityl-1H-indazole (800 mg, 1.6 mmol) and 2M ethyl amine in THF (20 mL) was heated in a sealed tube at 80° C. for four days. Cooled to room temperature and concentrated. The crude product was purified by column chromatography on silica get eluting with a solution of ethyl acetate in hexane (1:1) to give the title compound (300 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-4b87ae52ca2f490c8091f8ec7c3c0460
Source noteuspto-grants-2013_10