HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → beta-Oxo-alpha-(3-pyridylcarbamoyl)-beta-(1-methyl-2-pyrrolyl)propionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Isocyanatopyridine | HCID 2760493 | — |
| Reactant | 3-(1-Methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile | HCID 2777170 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | beta-Oxo-alpha-(3-pyridylcarbamoyl)-beta-(1-methyl-2-pyrrolyl)propionitrile | HCID 86739305 | — |
Reaction Steps
To the suspension of 12.9 g of 1-methyl-β-oxo-2-pyrrolepropionitrile (U.S. Pat. No. 4,256,759) in 150 ml of dry toluene and 10.1 g of anhydrous triethylamine are added 10.8 g of 3-pyridyl isocyanate while stirring. After all solids are dissolved, the solution is allowed to stand at room temperature overnight. The mixture is evaporated to dryness, the residue taken up in methanol and the solution is neutralized to pH ca. 6 with 3 N hydrochloric acid and diluted with 600 ml of water. The resulting precipitate is collected, washed with water, and dried to yield the β-oxo-α-(3-pyridylcarbamoyl)-β-(1-methyl-2-pyrrolyl)propionitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435407 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-f707f20d2ce2441a9ac3e8795478da11 |
| Source note | uspto-grants-1984_03 |