HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-[3-(4-Methylphenyl)-1,2,4-thiadiazol-5-yl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole | HCID 22611066 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[3-(4-Methylphenyl)-1,2,4-thiadiazol-5-yl]piperazine | HCID 57712258 | — |
Reaction Steps
A mixture of 5-chloro-3-p-tolyl-1,2,4-thiadiazole (900 mg, 4.27 mmol) and piperazine (1.84 g, 21.4 mmol) in 25 mL EtOH were heated to reflux and stirred for 1 h at this temperature. The resulting yellow solution was cooled to room temperature and concentrated in vacuo. The residue was purified by flash column chromatography on silica eluting with a gradient formed from DCM, MeOH and NEt3 to yield after evaporation of the product containing fractions 1.1 g (99%) of the title compound as light yellow solid. MS (m/e): 261.3 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023852B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-9fe83ad1164b457095a0afb5f3d5d9e5 |
| Source note | uspto-grants-2015_05 |