HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 12969097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178510311 | HCID 178510311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12969097 | HCID 12969097 | 38% |
Reaction Steps
To a suspension of 4-hydroxy-6-(3-morpholin-4-yl-propoxy)-[1.5]naphthyridine-3-carbonitrile in anhydrous CH2Cl2 (150 ml) was added oxalyl chloride (2.7 ml, 31.8 mmol) and DMF (0.1 ml, 20%) at room temperature under nitrogen. The suspension became a clear dark brown solution. The resulting mixture was stirred for an additional 1 hr. The solvent was removed by rotary evaporation. The residue was dissolved in ice-water mixture, made basic with (NH4OH), and extracted with CH2Cl2. The extracts were washed (brine), dried (Na2SO4), and concentrated to give the title compound (400 mg, 38%). H-NMR δ(DMSO-d6): 1.88 (2H, m), 2.26-2.29 (6H, m), 2.51 (2H, m), 3.49 (2H,m), 4.34 (2H, m), 6.834 (1H, d, C7-H), 8.147 (1H, d, C8-H), 8.711 (1H, s, C2-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06355636B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-0cafeac7227546ad8b45d56d8cf38d59 |
| Source note | uspto-grants-2002_03 |