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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251260Generated: November 3, 2026

2-Methoxyethanol → HCID 22502472, compound

https://huagongshe.com/reaction/1251260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22502633HCID 22502633—
ProductHCID 22502472HCID 22502472—

Reaction Steps

60% oily sodium hydride (0.20 g) was added gradually to 2-methoxyethanol (50 ml), under ice-cooling. To the resulting solution was added 1-(4-ethylpiperazin-1-yl)-3-(2-chloropyridin-4-yl)isoquinoline (0.20 g) obtained in the previous Example, and the mixture was heated under reflux for 3 days. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and purified water. The ethyl acetate layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give the title compound (0.12 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-ad66c7d82f5a45d9821124db144feeb7
Source noteuspto-grants-2002_01