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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523977Generated: October 29, 2026

Glycine → N-(4-Hydroxy-1-methyl-8-phenoxyisoquinoline-3-carbonyl)glycine

https://huagongshe.com/reaction/523977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 90024444HCID 90024444—
SolventMethanolHCID 887—
ProductN-(4-Hydroxy-1-methyl-8-phenoxyisoquinoline-3-carbonyl)glycineHCID 15941629—

Reaction Conditions

Temperature110 °C

Reaction Steps

A pressure glass reaction flask which included top threads for a screw cap lid can be fitted with a magnetic stirrer, charged with 4e, glycine (about 3 molar equivalents), methanol, and a sodium methoxide solution (with 1.2 molar eqivalents NaOCH3) and sealed. The reaction can then be heated to 110° C. for at least 6 h during which time the reaction forms a yellow suspension. The reaction can then be cooled to 20-25° C. and evaluated by HPLC. The reaction can be continued until less than 1% 4e remains as determined by HPLC, filtered, washed with methanol, dried under vacuum, dissolved in water and extracted with ethyl acetate to remove impurities to below 0.1%. The ethyl acetate can be removed and an acetic acid solution (with 3 molar eqivalents acetic acid) can be added over one hour. The suspension can be stirred at room temperature for at least 3 hours, filtered, and the solid washed with water (3×), cold acetone (5-10° C., 2×) and evaluated for impurities by HPLC. If acetone removable impurities are present, the flask can be charged with acetone and refluxed for at least 8 h, slowly cooled to 5-10° C., stirred for at least 2-3 h, filtered, washed with cold acetone (5-10° C., 3×) and dried under vacuum to obtain 2-(4-hydroxy-1-methyl-8-phenoxyisoquinoline-3-carboxamido)acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340511B2
Source datasetuspto-grants-2016_05
ORD IDord-af10079d06ab4c4cbf7ceffab27fef61
Source noteuspto-grants-2016_05