HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroethyl chloroformate → (2S)-1-Methyl-2-[2-(methylsulfanyl)ethyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | (S)-4-Benzyl-1-methyl-2-(2-methylsulfanyl-ethyl)-piperazine | HCID 58626059 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Ammonia methanol | HCID 21705897 | — |
| Product | (2S)-1-Methyl-2-[2-(methylsulfanyl)ethyl]piperazine | HCID 45099614 | 118.1% |
Reaction Steps
To a cold solution of (S)-4-benzyl-1-methyl-2-(2-methylsulfanyl-ethyl)-piperazine (0.450 g, 1.7 mmol) in 1,2-dichloroethane (5.0 mL) is added dropwise 1-chloroethyl chloroformate (0.24 mL, 2.2 mmol). After stirring at ambient temperature for 18 hours, the 1,2-dichloroethane is evaporated and 40 mL of methanol is added to the residue. This solution is refluxed for 2 hours. Evaporation of the methanol gives the crude product. Silica gel chromatography, eluting with methylene chloride:2N ammonia/methanol (90:10), gives 0.175 g of the title compound as a light yellow oil; mass spectrum (ion spray): m/z=175 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384934B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-82aa3edd489a4eaab94e85b3ba1aa991 |
| Source note | uspto-grants-2008_06 |