HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 5-(4-Methyl-1-piperazinyl)-1,3,4-thiadiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 86606224 | HCID 86606224 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 5-(4-Methyl-1-piperazinyl)-1,3,4-thiadiazol-2-amine | HCID 1500023 | — |
Reaction Steps
A mixture of 1-methylpiperazine (0.742 ml, 6.6 mmol) and bromo-[1,3,4]thiadiazol-2-ylamine (63a) (0.60 g, 3.3 mmol) in n-propanol (15 ml) is heated at reflux for 6 hours. After cooling to room temperature the solvent is removed and the residue is trituated with ethyl acetate and methanol to afford the required compound as a pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017608B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-95f8c4dcb3e44a7db815d566ccac8e7a |
| Source note | uspto-grants-2011_09 |