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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 644952Erstellt: 24. Oktober 2026

Imidazole → HCID 23525647, Verbindung

https://huagongshe.com/de/reaction/644952

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
EduktTert-Butyl 4-{4-Chloro-2-[(1R)-1-Hydroxyethyl]Phenyl}-3,6-Dihydropyridine-1(2H)-CarboxylateHCID 68519018—
KatalysatorZinc azideHCID 178514646—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 23525647HCID 23525647—

Reaktionsschritte

A solution of diethyl azodicarboxylate (49.6 mL, 0.315 mol) was added dropwise to a stirred mixture of tert-butyl 4-{4-chloro-2-[(1R)-1-hydroxyethyl]phenyl}-3,6-dihydropyridine-1(2H)-carboxylate (26.7 g, 78.9 mmol), Zn(N3)2.2Py (prepared according to: Viaud, M-C; Rollin, P. Synthesis 1990:130-131) (48.5 g, 0.158 mol), triphenylphosphine (82.7 g, 0.315 mol) and imidazole (21.5 g, 0.315 mol) in dichloromethane at approximately 0° C. After the addition, the resulting mixture was allowed to warm to ambient temperature and stirred vigorously for 3 days. The reaction mixture was filtered through a short column of silica gel eluted with the appropriate volume of dichloromethane to remove excess salts and polar byproducts. The filtrate was concentrated in vacuo and the crude residue was purified by flash chromatography on silica gel (12.5% ethyl acetate/hexanes as eluent) to furnish the title compound as a viscous pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07700778B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-9817cd2b1e83400ea35ce1dd8e1b184e
Quellennotizuspto-grants-2010_04