HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-[(2-Oxopropyl)amino]pyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-(Methylamino)pyridine-3-carboxylic acid | HCID 22271415 | — |
| Product | 6-[(2-Oxopropyl)amino]pyridine-3-carboxylic acid | HCID 18753312 | — |
Reaction Steps
A 1.5 g portion of 6-methylaminonicotinic acid in 20 ml of acetic anhydride was heated under reflux for 1.5 hours. After evaporation of the solvent under reduced pressure, the residue was dissolved with saturated aqueous sodium bicarbonate, and the aqueous layer was washed with ethyl acetate and then adjusted to pH 3 using concentrated hydrochloric acid. Then the aqueous layer was extracted with chloroform, the organic layer was washed and dried, and then the solvent was evaporated under reduced pressure to obtain 280 mg of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673799B1 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-959d8bb651d44dfabb5de79cbff7b980 |
| Source note | uspto-grants-2004_01 |