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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269737Generated: October 28, 2026

Water → HCID 69430818, compound

https://huagongshe.com/reaction/1269737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BenzylpiperazineHCID 75994—
ReactantSodium t-butoxideHCID 23676156—
Reactant5-bromo-1-(oxan-2-yl)-1H-indazoleHCID 53433826—
CatalystHCID 178424406HCID 178424406—
SolventTolueneHCID 1140—
ProductHCID 69430818HCID 6943081855%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of the 5-bromo-1-tetrahydro-2H-pyran-2-yl-1H-indazole (250 mg, 0.889 mmol) obtained in Reference Example 5 in toluene (12 ml) were added 1-benzylpiperazine (0.24 ml, 1.35 mmol) and sodium tert-butoxide (128 mg, 1.33 mmol) at room temperature. After deaeration, bis(tri-o-tolylphosphine)-palladium(II) dichloride (70 mg, 0.0891 mmol) was added thereto and the resulting mixture was stirred at 75° C. for three and a half hours. Then, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: chloroform/ethyl acetate=5/2) to obtain 5-(4-benzyl-1-piperazinyl)-1-tetrahydro-2H-pyran-2-yl-1H-indazole (183 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-323bb652347d4d1c9fc88a7634e45af0
Source noteuspto-grants-2007_04