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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 711205Erstellt: 24. Oktober 2026

Triphenylphosphine → HCID 117729796, Verbindung

https://huagongshe.com/de/reaction/711205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiethyl azodicarboxylateHCID 5462977—
Edukt3-Tetrahydropyranyloxy-1-propanolHCID 10855766—
Edukt5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenolHCID 68952645—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 117729796HCID 11772979696%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 5-(5-amino-3-tert-butyl-pyrazol-1-yl)-2-chloro-phenol (WO20111154734A1, which is incorporated herein by reference in it is entirety; 500 mg, 1.88 mmol), and Ph3P (986 mg, 3.76 mmol) in dry THF (10 mL) was added 3-(tetrahydro-pyran-2-yloxy)-propan-1-ol (Can. J. Chem. Vol. 73, 1195, pp 1682, which is incorporated herein by reference in it is entirety; 452 mg, 2.82 mmol). The resulting mixture was cooled to 0° C. using an ice bath and diethylazodicarboxylate (0.69 mL, 3.76 mmol) was added to the chilled mixture which was allowed to warm up to RT. The volatiles were removed under reduced pressure. The residue was purified by FCC, using 0-50% EtOAc in cyclohexane, to give the title compound (739 mg, 96%). LCMS (Method 1): Rt 3.63 min, m/z 408 [MH+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181242B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-b73e8e1c9ed743cb835b20907910d998
Quellennotizuspto-grants-2015_11