HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 3-Cyano-5-(4-fluorophenyl)-4-methyl-2-morpholinopyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Ethyl 2-cyanoethanecarboximidate | HCID 256188 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)propan-1-one | HCID 13051652 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 3-Amino-3-morpholinoacrylonitrile | HCID 2763631 | — |
| Product | 3-Cyano-5-(4-fluorophenyl)-4-methyl-2-morpholinopyrrole | HCID 15871297 | 4.7% |
Reaction Steps
In anhydrous ethanol (10 ml) was dissolved 3-amino-3-morpholinoacrylonitrile, as prepared from ethyl 2-cyano-acetimidate (1.0 g) and morpholine (0.78 g) as in Reference Example 3, followed by addition of sodium hydrogen carbonate (0.95 g). Then, a solution of 2-bromo-4′-fluoropropiophenone (2.06 g) in ethanol was added dropwise thereto at room temperature with stirring. The mixture was refluxed for 10 minutes and, then, stirred at room temperature overnight. The separated crystal crop was collected by filtration and recrystallized from ethanol to provide the title compound as colorless crystals (0.12 g). m.p. 245-247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172102B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-5d75846c7ee841dbba65f3b2e16abd9a |
| Source note | uspto-grants-2001_01 |