HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 70921741, compound → N-(4-(4-Aminophenoxy)pyridin-2-yl)-2-methoxyacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 70921741 | HCID 70921741 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | N-(4-(4-Aminophenoxy)pyridin-2-yl)-2-methoxyacetamide | HCID 86660483 | — |
Reaction Steps
A solution of 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide (730 mg, 2.41 mmol) in MeOH/DCM (1:1 v/v, 80 mL) containing AcOH (5 drops) was subjected to hydrogenation by passage through a Thales H-cube (1.0 mL min−1, RT, 70 mm 10% Pt/C Cat-Cart, full hydrogen mode) and was then evaporated in vacuo. The residue was partitioned between DCM (20 mL) and saturated aqueous NaHCO3 solution (10 mL). The organic layer was washed with brine (20 mL) and was dried (MgSO4) and evaporated in vacuo to afford the title compound, Intermediate H1, as a white solid (0.63 g, 91%); Rt 0.88 min (Method 2); m/z 274 (M+H)+ (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299074B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-06978fe4a3174253bc69875ca949a4d7 |
| Source note | uspto-grants-2012_10 |