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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269798Generated: October 31, 2026

Triphenylphosphine → HCID 22933553, compound

https://huagongshe.com/reaction/1269798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTetrahydro-4H-pyran-4-olHCID 74956—
Reactant1H-Indazol-5-olHCID 101438—
ReactantDiethylazodicarboxylate tolueneHCID 66777355—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22933553HCID 2293355347%

Reaction Steps

To a solution of the 1H-indazol-5-ol (150 mg, 1.12 mmol) obtained in Reference Example 4 in tetrahydrofuran (6 ml) were added 4-hydroxytetrahydropyran (0.107 ml, 1.12 mmol), triphenylphosphine (293 mg, 1.12 mmol) and a 40%-diethyl azodicarboxylate-toluene solution (0.517 ml, 1.14 mmol) at 0° C. After 30 minutes, the mixture thus obtained was heated to room temperature. After stirring overnight, the reaction solution was concentrated under reduced pressure, and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/methanol) to obtain 5-(tetrahydro-2H-pyran-4-yloxy)-1H-indazole (11.4 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-868589481e18464d8025e7f0bdb69e94
Source noteuspto-grants-2007_04