HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 7-[(4-Fluorophenyl)methyl]-4-hydroxy-N-(2-hydroxyethyl)-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Ethyl 7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxylate | HCID 69482570 | — |
| Product | 7-[(4-Fluorophenyl)methyl]-4-hydroxy-N-(2-hydroxyethyl)-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxamide | HCID 69480158 | — |
Reaction Steps
This compound was prepared from ethyl 7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxylate and 2-aminoethanol using methods similar to Example 563 to provide a white solid: 1H NMR (CDCl3) δ 10.42 (1H, b), 8.53 (1H, s), 8.25 (1H, s), 7.21-7.26 (2H, m), 6.97 (2H, t, J=8 Hz), 4.38 (2H, t, J=7 Hz), 4.15 (2H, s), 3.86 (2H, t, J=5 Hz), 3.49-3.66 (4H, m), 3.35 (2H, b), 2.85 (1H, t, J=5 Hz), 2.35 (2H, b), 1.72-1.76 (4H, m); ES+ MS: 483 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691991B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-5f04c09ea9eb44a4aa32414948a1375c |
| Source note | uspto-grants-2014_04 |