Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 23359031 | HCID 23359031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23359026 | HCID 23359026 | — |
Reaction Steps
To the thus obtained 2-(4-methyl-1-piperazinyl)-3,6-difluoro-4-chloro-5-nitrotoluene (0.13 g) are added anhydrous dimethylformamide (2 ml), potassium fluoride (37 mg) and cyclopropylamine (0.15 ml) and the mixture is stirred at 100° C. for 3 hours. After cooling, the reaction mixture is poured into ice-water, extracted with dichloromethane and the extract is dried. The solvent is distilled off under reduced pressure and purified by silica-gel column-chromatography (eluent; dichloromethane : methanol=10 : 1) to give 3-(4-methyl-1-piperazinyl)-4-fluoro-5-chloro-2-methyl-6 -nitro-N-cyclopropylaniline (0.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05495020 |
|---|
| Source dataset | uspto-grants-1996_02 |
|---|
| ORD ID | ord-308554e1ad9947829178e8d30d86e8dc |
|---|
| Source note | uspto-grants-1996_02 |
|---|