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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711205Generated: October 25, 2026

Triphenylphosphine → HCID 117729796, compound

https://huagongshe.com/reaction/711205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant3-Tetrahydropyranyloxy-1-propanolHCID 10855766—
Reactant5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenolHCID 68952645—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117729796HCID 11772979696%

Reaction Conditions

Temperature0 °C

Reaction Steps

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+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181242B2
Source datasetuspto-grants-2015_11
ORD IDord-b73e8e1c9ed743cb835b20907910d998
Source noteuspto-grants-2015_11