HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 22326795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 22326834 | HCID 22326834 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22326795 | HCID 22326795 | — |
Reaction Steps
A mixture of 1-(2-chloroethoxy)-2,3-dimethoxy-5-nitrobenzene (1.382 g, 5.28 mmol), K2CO3 (1.83 g, 13.2 mmol), and N-methylpiperazine (1.76 mL, 15.85 mmol) was stirred and heated under N2 in CH3CN (20 mL) under reflux overnight. The next day 0.80 g K2CO3 and 0.66 mL piperazine were added (1.1 eq.) and heated for 3 h more when HPLC showed that the reaction was complete. The solids were filtered and washed well with CH3CN and the filtrate was evaporated at 80° C. to remove excess amine. The resulting red oil was dissolved in CH2Cl2 and washed with water. The aqueous layer was washed with CH2Cl2. The combined organic layers were dried and evaporated giving 2,3-dimethoxy-1-(2-(4-methylpiperazin-1-yl)ethoxy)-5-nitrobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939874B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-6f6b830d5b124ba48cf853e7d664df0f |
| Source note | uspto-grants-2005_09 |