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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383994Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/383994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,3,4-Tetrahydro-1-phenylisoquinolineHCID 100137—
EduktCarbodiimideHCID 160435—
EduktDichloromethane ethanolHCID 21584144—
Edukt4-Oxo-4-(3-(trifluoromethyl)benzylamino)butyric acidHCID 43397104—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amideHCID 4621391662%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367700B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-38e2fcc0283d45a5b68f1653fc06f081
Quellennotizuspto-grants-2013_02