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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098906Generated: October 26, 2026

Butyronitrile → 1-Methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine

https://huagongshe.com/reaction/1098906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyronitrileHCID 8008—
ReactantPhenylpropanolamineHCID 10297—
ReactantCesium carbonateHCID 10796—
Reactant5-iodo-1-pyridin-2-yl-1H-indazoleHCID 59339792—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Product1-Methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamineHCID 6681299816.3%

Reaction Conditions

Temperature125 °C

Reaction Steps

5-Iodo-1-pyridin-2-yl-1H-indazole (118b, 81 mg, 0.25 mmol), (1R,2S)-(−)-norephedrine (119 mg, 0.79 mmol) and butyronitrile (3 ml) were charged in a 7 ml vial. Copper(I) iodide (5.8 mg, 0.1 mol %) and cesium carbonate (261 mg, 0.8 mmol) were added, the vial was sealed and the solution was stirred (magnetic bar) at 125° C. for 2 h. Inorganic material was filtered off, and washed with ethyl acetate. The ethyl acetate phase was collected and concentrated and purified on silica with methanol:ethyl acetate 0:100 to 30:70 over 45 min. Pure fractions were pooled and concentrated to give 14 mg (16%) of 1-methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143290B2
Source datasetuspto-grants-2012_03
ORD IDord-421f83de2e124eec958255a2458ab25e
Source noteuspto-grants-2012_03