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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714805Generated: November 3, 2026

Water → 1-(2-Benzo[1,3]dioxol-5-ylmethyl-1-tert-butoxycarbonylpiperazin-4-yl)-7-methoxyisoquinoline

https://huagongshe.com/reaction/1714805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-7-methoxyisoquinolineHCID 22250181—
Reactant2-Benzo[1,3]dioxol-5-ylmethyl-1-tert-butoxycarbonylpiperazineHCID 23155618—
SolventEthylene GlycolHCID 174—
Product1-(2-Benzo[1,3]dioxol-5-ylmethyl-1-tert-butoxycarbonylpiperazin-4-yl)-7-methoxyisoquinolineHCID 2315580144%

Reaction Steps

A mixture of 320 mg of 2-benzo[1,3]dioxol-5-ylmethyl-1-tert-butoxycarbonylpiperazine as synthesized in the above step, 200 mg of 1-chloro-7-methoxyisoquinoline and 100 mg of triethylamine was stirred in 2 ml of ethylene glycol at 150° C. for 18 hours. After addition of water, the solution was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified on silica gel column chromatography (ethyl acetate:n-hexane=1:1) to provide 210 mg (44%) of 1-(2-benzo[1,3]dioxol-5-ylmethyl-1-tert-butoxycarbonylpiperazin-4-yl)-7-methoxyisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-89884b65e752497cbe03964188c7a8bd
Source noteuspto-grants-2010_09