HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine-3-carboxamide → HCID 135899198, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine-3-carboxamide | HCID 506623 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | [2-(3-Fluoro-phenyl)-ethoxy]-acetic acid methyl ester | HCID 67099252 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 135899198 | HCID 135899198 | 55% |
Reaction Steps
A suspension of 2-amino-nicotinamide (250 mg, 1.82 mmol) and [2-(3-fluoro-phenyl)-ethoxy]-acetic acid methyl ester (464 mg, 2.18 mmol) in THF (5 ml) was treated with LiHMDS (1M THF solution, 4.6 ml) overnight at ambient temperature. The yellow suspension was filtrated, the filtrate was brought to dryness and the residue was purified by column chromatography (amino-phase silica gel, CH2Cl2/MeOH, 19/1) to give 2-[2-(3-fluoro-phenyl)-ethoxymethyl]-3H-pyrido[2,3-d]pyrimidin-4-one (303 mg, 1 mmol; 55%) as white solid. MS (m/e): 300.2 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572801B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-83bbf18ddbb443179660ee0a8c4a151e |
| Source note | uspto-grants-2009_08 |