HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetyl-3-pyridinecarboxylic acid → HCID 178467407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetyl-3-pyridinecarboxylic acid | HCID 10176278 | — |
| Reactant | 3-Amino-1-(3,5-difluorophenyl)urea | HCID 15278687 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178467407 | HCID 178467407 | — |
Reaction Steps
To 50 mg of 2-acetylnicotinic acid are added 56 mg of 4-(3,5-difluorophenyl)semicarbazide and 1 mL of methanol. After a minute of stirring the product begins precipitating from the solution. After stirring overnight (15 h) the stir vane is removed and rinsed with 0.2 mL of methanol. The reaction mixture is centrifuged and the supernatant solution removed. In the same way the solid is rinsed with methanol (3×0.5 mL) and ether (1×0.5 mL). The solid is dried in vacuo with heating to give 2-acetylnicotinic acid 4-(3,5-difluorophenyl)semicarbazone (also known as 2-[methyl-{[(3,5-difluorophenylamino)carbonyl]hydrazono}methyl]-3-pyridine-carboxylic acid), m.p. 186° (compound 31, Table A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05098466 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-6f8d91d8f9574f7385d242225ff1c001 |
| Source note | uspto-grants-1992_03 |