HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetate → Methyl [1-(5-aminopyridin-2-yl)piperidine-4-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetate | HCID 47357980 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl [1-(5-aminopyridin-2-yl)piperidine-4-yl]acetate | HCID 59464078 | 85.8% |
Reaction Steps
A solution of methyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetate (710 mg, 2.60 mmol) in EtOH (26 mL) was treated with 10% Pd on charcoal (71 mg), and stirred vigorously under an atmosphere of hydrogen for 4 h. The reaction mixture was filtered through diatomaceous earth and the filtrate was evaporated to dryness to give the title compound (556 mg, 70%) as an oil; 1H NMR δ 1.12-1.27 (2H, m), 1.67 (2H, d), 1.75-1.89 (1H, m), 2.25 (2H, d), 2.56 (2H, t), 3.33 (2H, s), 3.58 (3H, s), 4.52 (2H, s), 6.61 (1H, d), 6.86-6.93 (1H, m), 7.58 (1H, d); MS m/e MH+ 250.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795283B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-97b9017391684f28993846c1aa9fbcfd |
| Source note | uspto-grants-2010_09 |