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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860013Generated: October 26, 2026

Piperazine → 8-Methyl-2-piperazin-1-ylmethyl-2,3-dihydro[1,4]dioxino[2,3-f]quinoline

https://huagongshe.com/reaction/860013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium BicarbonateHCID 516892—
Reactant[(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl4-bromobenzenesulfonateHCID 20624762—
SolventDimethyl SulfoxideHCID 679—
Product8-Methyl-2-piperazin-1-ylmethyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolineHCID 6960502582%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of [(2R)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl-4-bromobenzene sulfonate (1.35 g, 3 mmol) and piperazine (2.58 g, 30 mmol) in dimethylsulfoxide (16 mL) is heated at 75° C. under nitrogen for 1 hour, cooled and poured into saturated aqueous sodium bicarbonate. The mixture is extracted with ethyl acetate and the extracts are dried over anhydrous magnesium sulfate and evaporated to dryness. The residue is flash chromatographed on silica gel Merck-60 using a gradient of methanol (5–25%) in dichloromethane containing 0.2% ammonium hydroxide to provide the title compound as an off-white oil (0.736 g) identical to the compound of example 1B, step B′.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153849B2
Source datasetuspto-grants-2006_12
ORD IDord-4e16f9c37a774cb5adc9d1ffda09405d
Source noteuspto-grants-2006_12