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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398356Generated: October 30, 2026

1H-Indazole-5-carbonitrile → 5-(Aminomethyl)-1H-indazole

https://huagongshe.com/reaction/398356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazole-5-carbonitrileHCID 11126384—
SolventTetrahydrofuranHCID 8028—
Product5-(Aminomethyl)-1H-indazoleHCID 12096223—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of LiAl H4 (0.76 g, 20.1 mmol) in THF (10 mL) cooled to 0° C. was added a solution of 5-cyanoindazole (0.64 g, 4.47 mmol) in THF (10 mL) dropwise. After 0.5 h the reaction mixture was warmed to reflux for 2 h, then cooled to 0° C. and quenched by the careful addition of water (0.76 mL), 1.0 N sodium hydroxide (0.76 mL), and water (2.28 mL). This mixture was filtered through a pad of celite and washed with THF/MeOH (3:1, 300 mL). Removal of the solvent in vacuo provided a solid which was purified via flash column chromatography (25×150 mm column; elution with MeOH:CH2Cl2:CH2Cl2 saturated with NH3, 10:60:30). This afforded the title compound as a light yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610692B1
Source datasetuspto-grants-2003_08
ORD IDord-5002a3a397694005bff0f67d171d89d0
Source noteuspto-grants-2003_08