Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79423Generated: October 26, 2026

Ammonium Chloride → 3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazole-4-amine

https://huagongshe.com/reaction/79423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazoleHCID 67260809—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
Product3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazole-4-amineHCID 6725927284.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 3-cyclopropyl-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole (22.01 g, 71.38 mmol) in EtOH/H2O (200 mL/50 mL) was added iron powder (79.73 g, 1428 mmol) and NH4Cl (3.818 g, 71.38 mmol). The reaction mixture was heated to reflux for three hours, cooled to 60° C. and filtered through a pad of Celite. The pad of Celite was washed with 20:1 EtOH/Et3N (800 mL) and 1:1 MeOH/DCM (600 mL). The combined filtrate was concentrated under reduced pressure. The residue was dissolved in EtOAc (800 mL), washed with saturated NaHCO3 aqueous solution, dried (Na2SO4) and concentrated under reduced pressure to give the product (16.87 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-23a6bef378da49d3a527ffbf1fd547a2
Source noteuspto-grants-2014_09