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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875699Generated: October 30, 2026

Phosphoric Acid → (R)-3-[2-(2-hydroxymethylpyrrolidin-1-yl)ethyl]-5-methyl-2H-isoquinolin-1-one hemiphosphate monohydrate

https://huagongshe.com/reaction/1875699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
Reactant(R)-3-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-5-methylisoquinolin-1(2H)-oneHCID 10424118—
SolventEthanolHCID 702—
Product(R)-3-[2-(2-hydroxymethylpyrrolidin-1-yl)ethyl]-5-methyl-2H-isoquinolin-1-one hemiphosphate monohydrateHCID 131730055—

Reaction Steps

A free form (502 mg) of (R)-3-[2-(2-hydroxymethylpyrrolidin-1-yl)ethyl]-5-methyl-2H-isoquinolin-1-one was measured in a reaction test tube, aqueous ethanol (5.8 mL, ethanol:water=8:1) was added and the mixture was completely dissolved by heating under reflux. Thereto was added aqueous phosphoric acid solution (501 μL, solution prepared by diluting commercially available 85% phosphoric acid (2.02 g) with the above-mentioned aqueous ethanol to scale up to 10 mL), and the mixture was stirred at room temperature for one day and left standing. The precipitate was collected by filtration. The precipitate (301 mg) was measured in a reaction test tube, and aqueous ethanol (2.6 mL, ethanol:water=4:1) was added. The mixture was completely dissolved by heating under reflux, stirred at room temperature for one day and left standing. The precipitate was collected by filtration, and dried under reduced pressure at 50° C. for 5 hr to give the title compound (264 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309573B2
Source datasetuspto-grants-2012_11
ORD IDord-dcbbf5c62a2b4f518fbbb8c86080128d
Source noteuspto-grants-2012_11