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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218162Generated: October 27, 2026

Nitrogen → 1-(4-Fluorophenyl)-1h-indazol-5-amine

https://huagongshe.com/reaction/218162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant4-FluoroiodobenzeneHCID 9605—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1H-Indazol-5-amineHCID 88012—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Fluorophenyl)-1h-indazol-5-amineHCID 592357271,090.4%

Reaction Steps

Commercially available 5-aminoindazole (15 g, 113 mmol) was dissolved in 100 mL dry dioxane in a stainless steel pressure bottle followed by the addition of trans-1,2-diaminocyclohexane (6.4 g, 56 mmol), CuI (2.1 g, 11.3 mmol), K3PO4 (43 g, 203 mmol), and 1-fluoro-4-iodobenzene (27.5 g, 11.3 mmol). The reactor was sealed and heated at 120 C for 72 h under a blanket of N2. The reaction was filtered through a large SiO2 plug on a fitted funnel using EtOAc until the eluent ran clear (˜1 L). The solution was concentrated in vacuo and the dark brown solid was taken up in hot EtOAc (˜150 mL) and hexane was added to induce precipitation. The dark black solid was filtered and dried under vacuum to give 28 g (73%) of pure N1-(4-fluorophenyl)-5-aminoindazole. MS found: (M+H)+=228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198311B2
Source datasetuspto-grants-2012_06
ORD IDord-5915d7d6f29240e29f83736f394fc4a3
Source noteuspto-grants-2012_06