HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 1H-Indole-3-propanoic acid, 2-methyl- | HCID 97380 | — |
| Edukt | 4-Benzyl-4-piperidinol | HCID 98152 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 1-[beta-(2-Methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine | HCID 21324671 | — |
Reaktionsschritte
To a stirred solution of 5.0 g of β-(2-methyl-3-indolyl)propionic acid and 2.5 g of triethylamine in 100 ml of chloroform was added dropwise 2.7 g of ethyl chloroformate at a temperature below 0° C. After the addition was complete, stirring was continued for additional 15 minutes and thereto was added 4.7 g of 4-benzyl-4-hydroxypiperidine in several portions. The reaction mixture was stirred for 4 hours at room temperature and allowed to stand overnight. The reaction product was washed thoroughly with water and concentrated to dryness. The residue was recrystallized from ethanol to give 1-[β-(2-methyl-3-indolyl)propionyl]-4-benzyl-4-hydroxypiperidine, melting at 117°-119° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04148796 |
| Quelldatensatz | uspto-grants-1979_04 |
| ORD ID | ord-3024e340990f494fa08720f195cbe64d |
| Quellennotiz | uspto-grants-1979_04 |