Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,3-Difluoro-5-iodopyridine | HCID 11322427 | — |
| Reactant | HCID 178479278 | HCID 178479278 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178521606 | HCID 178521606 | 16% |
Reaction Steps
2,3-Difluoro-5-iodopyridine (300 mg, 1.24 mmol) was dissolved in dioxane (3 ml) and trans-4-aminocyclohexanol hydrochloride (227 mg, 1.49 mmol, 1.2 equiv.) and Cs2CO3 (1.01 g, 3.11 mmol, 2.5 equiv.) were added at room temperature. The mixture was stirred for 3 hours at 100° C. The reaction mixture was evaporated and treated with sat. NaHCO3 solution and extracted twice with a small volume of CH2Cl2. The organic layers were loaded directly to silica gel column and the crude material was purified by flash chromatography on silica gel (20 gr, ethyl acetate/heptane gradient, 0:100 to 0:100). The desired trans-4-(3-fluoro-5-iodopyridin-2-ylamino)cyclohexanol (65 mg, 16% yield) was obtained as a white solid, MS: m/e=337.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08716316B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-38bfc9fd52894867bc10e81b736dc829 |
|---|
| Source note | uspto-grants-2014_05 |
|---|