HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 5-Piperidin-1-yl-1,3,4-thiadiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-Chloro-1,3,4-thiadiazol-2-amine | HCID 314235 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Piperidin-1-yl-1,3,4-thiadiazol-2-amine | HCID 1500010 | — |
Reaction Steps
Piperidine (100 μl) was added to a solution of 2-amino-5-chloro-1,3,4-thiadiazole (50 mg) in ethanol (1 ml) and the mixture heated in a sealed vial at 70° C. for 6 hours The ethanol was evaporated from the cooled reaction under vacuum, the residue diluted with water and the solid product filtered off to give 2-amino-5-piperid-1-yl-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208629B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-d25a507e060d4028a335c8ac6b6f0fec |
| Source note | uspto-grants-2007_04 |