HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535089Erstellt: 25. Oktober 2026
Acetonitrile → Methyl (3r,4s)-1-[(z)-1-(methylthio)-2-nitrovinyl]-4-[(3r)-3-phenylpyrrolidin-1-yl]carbonylpiperidine-3-carboxylate
https://huagongshe.com/reaction/535089
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Edukt | (3r,4s)-4-((r)-3-Phenyl-pyrrolidine-1-carbonyl)-piperidine-3-carboxylic acid methyl ester | HCID 67304902 | — |
| Produkt | Methyl (3r,4s)-1-[(z)-1-(methylthio)-2-nitrovinyl]-4-[(3r)-3-phenylpyrrolidin-1-yl]carbonylpiperidine-3-carboxylate | HCID 67304566 | 53,4% |
Reaktionsschritte
To a stirred solution of (3R,4S)-4-((R)-3-phenyl-pyrrolidine-1-carbonyl)-piperidine-3-carboxylic acid methyl ester (3.10E2 mg, 0.000980 mol) in anhydrous acetonitrile (9.8 mL, 0.19 mol) at rt was added triethylamine (274 uL, 0.00196 mol) and 1,1-bis(methylthio)-2-nitroethylene (248 mg, 0.00147 mol). The reaction mixture was heated to reflux (oil bath temperature: 85° C.) for 19 h. The reaction mixture was concentrated in vacuo. The residue was purified by Combiflash with 40-95% EtOAc/Hex to give the product as a yellow viscous oil (227 mg, 53% in yield). MS (ESI): (M+H)+=434.1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08853243B2 |
|---|
| Quelldatensatz | uspto-grants-2014_10 |
|---|
| ORD ID | ord-29da9d92aa9f44a8ae644a0d3bb384bc |
|---|
| Quellennotiz | uspto-grants-2014_10 |
|---|