HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylpiperidine → 3-(3-(4-Methylpiperidino)-1,2,5-thiadiazol-4-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | 3-Chloro-4-(pyridin-3-yl)-1,2,5-thiadiazole | HCID 10488164 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-(4-Methylpiperidino)-1,2,5-thiadiazol-4-yl)pyridine | HCID 19075317 | — |
Reaction Steps
A solution of 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine (10.80 g, 4 mmol) and 4-methylpiperidine (1.96 g, 20 mmol) in DMF (10 ml) was heated at 100° C. for 3 h. After evaporation water was added to the residue and extracted with ether. The combined and dried organic phases were evaporated and the residue purified by column chromatography (SiO2, eluent: ethyl acetate/methylene chloride (1:2)). Yield: 0.8 g (77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05260311 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-9424db1be5c1493dab03199190450abe |
| Source note | uspto-grants-1993_11 |