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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75569Erstellt: 24. Oktober 2026

Triphenylphosphine → 3-tert-butyl-1-(3-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)phenyl)-1H-pyrazol-5-amine

https://huagongshe.com/de/reaction/75569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-(Oxan-2-yloxy)ethan-1-olHCID 4166833—
EduktDiisopropyl azodicarboxylateHCID 5363146—
Edukt3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenolHCID 59557966—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-tert-butyl-1-(3-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)phenyl)-1H-pyrazol-5-amineHCID 57925659—

Reaktionsschritte

DIAD (847 μL, 4.32 mmol) was added slowly to a solution of 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenol (for reference procedure see US 2006/35922, which is incorporated herein by reference in its entirety; 500 mg, 2.16 mmol), 2-(tetrahydro-pyran-2-yloxy)-ethanol (439 μL, 3.25 mmol), and triphenylphosphine (1.13 g, 4.32 mmol) in THF (10.0 mL) and stirred for 72 h. The reaction mixture was partitioned between EtOAc (75 mL) and H2O (75 mL), and the aqueous layer extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), filtered and evaporated in vacuo. Purification by FCC, using 5-60% EtOAc in cyclohexane, gave semi-pure title compound (1.26 g). This was used in the next reaction without further purification. LCMS (Method 4): Rt 2.77, m/z 360 [MH+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835431B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-29e5c06fb49144eabbbc02e7e390b5d8
Quellennotizuspto-grants-2014_09