HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[(2-methoxy-4-methylmercapto-benzoyl)-amino]-3-nitro-1H-pyridin-6-one → HCID 178418498, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[(2-methoxy-4-methylmercapto-benzoyl)-amino]-3-nitro-1H-pyridin-6-one | HCID 54451266 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 178418498 | HCID 178418498 | — |
Reaction Steps
An amount of 6.2 gm of 2-[(2-methoxy-4-methylmercapto-benzoyl)-amino]-3-nitro-1H-pyridin-6-one is dissolved in 370 ml of glacial acetic acid and hydrogenated with hydrogen in the presence of 6 gm of 10% palladium charcoal at ambient temperature under 5 bars of pressure (duration of reaction: two hours). The catalyst is filtered off, and the filtrate is refluxed for about 1.5 hours with stirring. Then, about 250 ml of the solvent is evaporated off, and the remaining solution is poured onto ice water and neutralized with ammonia. The precipitate obtained is recrystallized from methanol. Another fraction can be obtained by evaporating the mother liquors of crystallization and triturating the residue with ether:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04722929 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-635cfe2f33674766827bc3eaf4c9f1ef |
| Source note | uspto-grants-1988_02 |