Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2190334Erstellt: 25. Oktober 2026

1,1'-Carbonyldiimidazole → Tert-butyl 4-(2-(1-(3,3-diphenylpropyl)-3-(4-(4-(methylsulfonamido)phenyl)thiazol-2-yl)ureido)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2190334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-[4-(2-amino-4-thiazolyl)phenyl]MethanesulfonamideHCID 7063853—
EduktTert-butyl 4-(2-(3,3-diphenylpropylamino)ethyl)piperidine-1-carboxylateHCID 57586396—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmitteldichloromethane N,N-dimethylformamideHCID 22350042—
ProduktTert-butyl 4-(2-(1-(3,3-diphenylpropyl)-3-(4-(4-(methylsulfonamido)phenyl)thiazol-2-yl)ureido)ethyl)piperidine-1-carboxylateHCID 57586428—

Reaktionsschritte

DMAP (0.17 g, 1 0.4 mmol), CDI (0.23 g, 1.4 mmol) and N-(4-(2-aminothiazol-4-yl)phenyl)-methanesulfonamide (0.25 g, 0.93 mmol) were mixed together in DCM/DMF and then stirred overnight at room temperature. After 24 hrs a precipitate had formed. tert-butyl 4-(2-(3,3-diphenylpropylamino)ethyl)piperidine-1-carboxylate (0.39 g, 0.93 mmol) was then added and the resulting mixture stirred for a further 15 hrs. The crude mixture was concentrated under reduced pressure and the residue purified by combi-flash to give tert-butyl 4-(2-(1-(3,3-diphenylpropyl)-3-(4-(4-(methylsulfonamido)phenyl)thiazol-2-yl)ureido)ethyl)piperidine-1-carboxylate 49 as an oily solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08324396B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-af96ee9b87874216bf58ce5f0851774e
Quellennotizuspto-grants-2012_12