HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-{3-Nitroanilino}nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 19781717 | HCID 19781717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-{3-Nitroanilino}nicotinamide | HCID 901913 | 99% |
Reaction Steps
The 2-(3-nitroanilino)-3-chloroformylpyridine was dissolved in tetrahydrofuran (2000 ml) and 70 ml of 30% solution of NH4OH was added dropwise with stirring to the reaction mixture. The reaction mixture was stirred at room temperature for 18 hours. Water was added to the mixture to dissolve the solid ammonium chloride that was formed. The tetrahydrofuran was removed, and the resulting aqueous slurry was filtered and washed yielding a yellow solid. The solid was washed with water and air dried yielding 64.8 g (250 mmole, 99% yield) of 2-(3-nitroanilino)-3-carbamoylpyridine (mp 240°-241° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264437 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-4bd6a2deea71431aa59b211d8f9d0319 |
| Source note | uspto-grants-1993_11 |