HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloro-3-phenyl-1,2,4-thiadiazole | HCID 32262 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperidine-4-carboxylate | HCID 68779858 | 75.8% |
Reaction Steps
A mixed solution of ethyl isonipecotate (0.782 ml, 5.08 mmol), 5-chloro-3-phenyl-1,2,4-thiadiazole (1.00 g, 5.08 mmol) and triethylamine (0.708 ml, 5.08 mmol) in N,N-dimethylformamide (10 ml) was stirred at room temperature for 30 minutes. The reaction mixture was poured to water and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and ethyl acetate to yield 1.22 g (75.8%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851473B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-48be604d3c024e7288af592edde54e2e |
| Source note | uspto-grants-2010_12 |