HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518833Generated: October 30, 2026
Water → 1-Methyl-4-[5-nitro-6-(propan-2-yloxy)pyridin-2-yl]piperazine
https://huagongshe.com/reaction/518833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 6-Chloro-3-nitro-2-(propan-2-yloxy)pyridine | HCID 10846412 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Methyl-4-[5-nitro-6-(propan-2-yloxy)pyridin-2-yl]piperazine | HCID 86697999 | 73.4% |
Reaction Steps
463 mg of potassium carbonate and 224 mg of 1-methylpiperazine are added to a solution of 484 mg of 6-chloro-3-nitro-2-(propan-2-yloxy)pyridine in 4.45 ml of DMSO. The reaction medium is heated for 1 hour at 105° C. After cooling, the mixture is run into water and extracted with ethyl acetate. The organic phase is washed with a saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue is taken up in diisopropyl ether and the insoluble material is filtered off and dried under vacuum, so as to give 460 mg of 1-methyl-4-[5-nitro-6-(propan-2-yloxy)pyridin-2-yl]piperazine in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115140B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-ef3771fabe9341d3937b312a71e67fac |
|---|
| Source note | uspto-grants-2015_08 |
|---|