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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyronitrile | HCID 8008 | — |
| Reactant | Phenylpropanolamine | HCID 10297 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-iodo-1-pyridin-2-yl-1H-indazole | HCID 59339792 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | 1-Methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine | HCID 66812998 | 16.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08143290B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-421f83de2e124eec958255a2458ab25e |
|---|
| Source note | uspto-grants-2012_03 |
|---|