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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334432Generated: October 29, 2026

(4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)phenyl)methanol → 4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzaldehyde

https://huagongshe.com/reaction/334432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)phenyl)methanolHCID 68276396—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzaldehydeHCID 8668056850.3%

Reaction Steps

85 mg (0.982 mmol) of manganese dioxide is added at room temperature to a solution of (4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)phenyl)methanol (100 mg, 0.327 mmol) in a mixture of ethyl acetate (10 ml) and dichloromethane (9 ml). The reaction mixture is placed in an ultrasonic bath for 5 hours. The reaction mixture is filtered, the solvents are evaporated and the crude product is purified by chromatography to yield 50.0 mg (yield-50.3%) of (4-(4-methylpiperazine-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzaldehyde in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-896777f828a741d5a65ecebdae9bd437
Source noteuspto-grants-2014_11