HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylthiourea → HCID 178482535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylthiourea | HCID 2723631 | — |
| Reactant | tert-Butyl 4-(1-bromo-2-oxoethyl)piperidine-1-carboxylate | HCID 21912701 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178482535 | HCID 178482535 | 66.9% |
Reaction Steps
A solution of tert-butyl 4-(1-bromo-2-oxoethyl)-1-piperidinecarboxylate (21 g) and N,N′-dimethylthiourea (6.0 g) in ethanol (300 ml) was heated under reflux. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in ethyl acetate and water, and the aqueous layer was collected by separation. The residue was basified with an aqueous potassium carbonate solution and extracted with chloroform. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure to obtain the title compound as a pale yellow solid (12 g, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820673B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-482a37c0adcf46498db5e594ec78e44a |
| Source note | uspto-grants-2010_10 |