HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,2,3,4-Tetrahydro-1-phenylisoquinoline → 4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2,3,4-Tetrahydro-1-phenylisoquinoline | HCID 100137 | — |
| Edukt | Carbodiimide | HCID 160435 | — |
| Edukt | Dichloromethane ethanol | HCID 21584144 | — |
| Edukt | 4-Oxo-4-(3-(trifluoromethyl)benzylamino)butyric acid | HCID 43397104 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide | HCID 46213916 | 62% |
Reaktionsschritte
1.98 g (˜2.0 mmol) of PS carbodiimide resin were added to a solution of 209 mg (1.0 mmol) of 1-phenyl-1,2,3,4-tetrahydroisoquinoline and 275 mg (1.0 mmol) of 4-oxo-4-(3-(trifluoromethyl)benzylamino)butyric acid (intermediate VVV01) in a mixture of DCM and DMF (82 ml, 40:1 vv) and the mixture was shaken for 16 h at RT. Then the resin was filtered off and it was washed with DCM and MeOH. The filtrate was concentrated to small volume under vacuum. Column chromatography (DCM/EtOH 40:1) of the residue produced 287 mg (0.6 mmol, 62%) of 4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide. MS: m/z 467.2 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08367700B2 |
| Quelldatensatz | uspto-grants-2013_02 |
| ORD ID | ord-38e2fcc0283d45a5b68f1653fc06f081 |
| Quellennotiz | uspto-grants-2013_02 |