Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 90402579 | HCID 90402579 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 90402691 | HCID 90402691 | 81% |
Reaction Steps
2,4-Dimethyl-3-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)-6-nitropyridine (0.56 g, 1.8 mmol) and NH4Cl (2.76 g, 51.6 mmol) were combined in a solution of MeOH (8.6 mL) and THF (8.6 mL) and cooled to 0° C. Zinc powder (1.13 g, 17.2 mmol) was added portion-wise over 30 min and the reaction mixture was allowed to warm to RT and stirred vigorously for 12 h. EtOAc (100 mL) was added and the resultant suspension was filtered through a pad of diatomaceous earth. The filter cake was washed with EtOAc (3×10 mL) and the combined filtrates were concentrated in vacuo. The residue was purified by silica gel chromatography (MeOH/DCM) to afford 4,6-dimethyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-amine (0.41 g, 81%) as a light red solid. MS (ESI) m/z: 296.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193719B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-b96d52c011b14a2ca4866bcce8471614 |
|---|
| Source note | uspto-grants-2015_11 |
|---|