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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377797Generated: November 2, 2026

Acetonitrile → HCID 11382630, compound

https://huagongshe.com/reaction/2377797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11406408HCID 11406408—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11382630HCID 11382630—

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl 1-ethyl-6-(1-ethynylcyclohexylamino)-7-methyl-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylate (10 mg) was dissolved in 5 ml of dioxane, 2.5 equivalents of a 1 N NaOH solution were added, and the mixture was heated at 60° C. for 4 h. Removal of the solvent in vacuo was followed by chromatography on an HPLC system to purify the product. The pure product was isolated from the reaction solution by chromatography on an HPLC system. This entailed use of a Merck Purospher-RP18 column and an acetonitrile:water mixture as eluent; the initial acetonitrile content was 15% and rose to 95% over the course of 20 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470706B2
Source datasetuspto-grants-2008_12
ORD IDord-6be038b02a904dff9dfca22502a68590
Source noteuspto-grants-2008_12