HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Acetate → 1-(Methoxymethyl)-2-[(5-methylpyridin-2-yl)amino]-2-oxoethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2-bromo-3-methoxy-N-(5-methylpyridin-2-yl)propanamide | HCID 57438618 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(Methoxymethyl)-2-[(5-methylpyridin-2-yl)amino]-2-oxoethyl acetate | HCID 57504570 | 88.9% |
Reaction Steps
Potassium acetate (2.01 g, 20.50 mmol) was added to a stirred solution of 2-bromo-3-methoxy-N-(5-methylpyridin-2-yl)propanamide (Step 1) (1.40 g, 5.13 mmol) in ACN (20 mL). The reaction mixture was refluxed for 5 hrs. The reaction mixture was filtered and concentrated in vacuo. The residue was purified with column chromatography (silica gel, eluting with DCM/EtOAc:2/1) to give the title compound as a colourless solid (1.15 g), 1H NMR (300 MHz, CDCl3) δ 8.57 (br s, 1H), 8.11 (m, 2H), 7.52 (dd, 1H), 5.44 (dd, 1H), 3.89 (dd, 1H), 3.78 (dd, 1H), 3.39 (s, 3H), 2.30 (s, 3H), 2.25 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143263B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-c360b38560c84d58adfb787f66a5ca31 |
| Source note | uspto-grants-2012_03 |