Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572060Generated: October 26, 2026

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

https://huagongshe.com/reaction/572060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-(Oxan-2-yloxy)ethan-1-olHCID 4166833—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenolHCID 59557966—
SolventTetrahydrofuranHCID 8028—
Product3-tert-butyl-1-(3-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)phenyl)-1H-pyrazol-5-amineHCID 57925659—

Reaction Steps

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+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029373B2
Source datasetuspto-grants-2015_05
ORD IDord-0e408a2c1d38407ebf4ebda707399290
Source noteuspto-grants-2015_05