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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745814Generated: November 1, 2026

Acetic Acid → HCID 86588462, compound

https://huagongshe.com/reaction/1745814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 69201512HCID 69201512—
SolventMethanolHCID 887—
ProductHCID 86588462HCID 86588462—

Reaction Steps

To a solution of (6-trimethylsilanylethynyl-isoquinolin-4-yl)-acetic acid methyl ester, as prepared for Intermediate 32 (0.19 g, 0.64 mmol), in anhydrous methanol (7 ml) is added K2CO3 (72 mg) and the resulting mixture stirred for 1 h. Additional K2CO3 (11 mg) is then added and stirring continued for 30 min. The mixture is then neutralised with glacial acetic acid and concentrated. Purification by flash silica column chromatography (ethylacetate/hexane 1:1) gives (6-ethynyl-isoquinolin-4-yl)-acetic acid methyl ester M+ 225. This intermediate (79 mg, 0.35 mmol) is dissolved in methanol under an inert atmosphere and 10% Pd on carbon (79 mg) added. The resulting suspension is stirred vigorously under an atmosphere of gaseous hydrogen. After 90 mins, filtration, washing with methanol and concentration give (6-ethyl-isoquinolin-4-yl)-acetic acid methyl ester M+ 229. To a solution of this intermediate (68 mg, 0.30 mmol) in THF/methanol/water (3:1:1, 3.5 ml) is added LiOH (12.5 mg) and the mixture stirred for 20 h at room temperature. Concentration under reduced pressure gives lithium (6-ethyl-isoquinolin-4-yl)-acetate M+ 221.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019136B2
Source datasetuspto-grants-2006_03
ORD IDord-67f305a0be4e47359685e31dacc2748f
Source noteuspto-grants-2006_03