HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 2,3-dihydro-1H-indole-1-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Edukt | (+) (2aS,4R)-6-acetyl-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indol | HCID 18652841 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,3-dihydro-1H-indole-1-carboxamide | HCID 771524 | 270,4% |
Reaktionsschritte
To a solution of (+)(2aS,4R)-6-acetyl-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole (1.7 g, 5.7 mmol) and triethylamine (0.8 ml, 6 mmol) in 90 ml CH2Cl2 was added dropwise a solution of 2,2,2-trichloroethylchloroformate (1.3 g, 6 mmol) in 10 ml CH2Cl2. The reaction mixture was stirred at room temperature for one hour and then extracted with water and 1N HCl. The organic solution was washed with a saturated NaHCO3 solution, a saturated brine solution, dried over MgSO4 and then concentrated to dryness in vacuo to give 2.5 g of the 1-carbamylindoline.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05624944 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-4759f96742e4405d80aa7044ee4bf327 |
| Quellennotiz | uspto-grants-1997_04 |