HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 13365280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | 4-[4-(Dimethylamino)phenyl]-2-(methylsulfanyl)-5-oxo-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrrole-3-carbonitrile | HCID 13236202 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13365280 | HCID 13365280 | 41.4% |
Reaction Steps
A suspension of 3.5 g 4-(4-dimethylaminophenyl)-2-methylthio-5-oxo-4-(3-pyridyl)-2-pyrroline-3-carbonitrile and 0.3 g sodium hydride (80% in white oil) is refluxed for one hour. One then adds dropwise thereto, within ten minutes, a solution of 1.3 g 3-dimethylaminopropyl chloride in 25 ml abs. dioxan and further boils for six hours. After cooling, the reaction mixture is filtered, the solvent is removed on a Rotavapor and the residue is chromatographed on silica gel with chloroform+methanol 10+1 as elution agent. After crystallization of the main fraction from isopropanol, one obtains 1.8 g of colorless crystals of mp 90°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04499089 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-0b9af09f6446479f877c6223c5568365 |
| Source note | uspto-grants-1985_02 |