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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402160Generated: 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/1402160

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 (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 Ph3P (1.13 g, 4.32 mmol) in THF (10.0 mL) and the mixture 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 the title compound (1.26 g). LCMS (Method 4): Rt 2.77, m/z 360 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907094B2
Source datasetuspto-grants-2014_12
ORD IDord-cc16255211d14d548ed1e28d12368cef
Source noteuspto-grants-2014_12