HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioacetamide → HCID 66673711, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | tert-Butyl 4-(bromoacetyl)piperazine-1-carboxylate | HCID 15829155 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66673711 | HCID 66673711 | 2.2% |
Reaction Steps
Thioacetamide (120 mg) was added to an ethanol (6 mL) solution of tert-butyl 4-(bromoacetyl)piperazinecarboxylate (340 mg) obtained in the above 1), and heated under reflux for 3 hours. The reaction liquid was restored to room temperature, then the solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=7/3) to obtain 7 mg of the entitled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101618B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-5049bb1cc5e24c538645131813f4771e |
| Source note | uspto-grants-2012_01 |