HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-Fluoro-4-(4-methyl-3-oxopiperazin-1-yl)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Reactant | 1-Methylpiperazin-2-one | HCID 4399042 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Fluoro-4-(4-methyl-3-oxopiperazin-1-yl)nitrobenzene | HCID 18783926 | — |
Reaction Steps
N,N-Diisopropylethylamine (11.5 ml) and 1-methyl-2-oxopiperazine (4.12 g) were added to a solution of 3,4-difluoronitrobenzene (1.82 ml) in acetonitrile (100 ml), and the mixture heated to reflux for 16 hours. Solvent was evaporated, and the residue chromatographed on silica, using as eluant a gradient increasing in polarity from 0 to 100% ethyl acetate in iso-hexane. Relevant fractions were combined and evaporated to give 3-fluoro-4-(4-methyl-3-oxopiperazin-1-yl)nitrobenzene (3.37 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06069145 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-f78ad015c006464ea31e376b16217840 |
| Source note | uspto-grants-2000_05 |