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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854704Generated: October 31, 2026

Acetic Acid → Etamicastat HCl salt

https://huagongshe.com/reaction/854704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantPotassium thiocyanateHCID 516872—
Reactant[4-(Tert-butyldimethylsilanyloxy)-3-oxobutyl]carbamic acid tert-butyl esterHCID 11493428—
Reactant(R)-6,8-difluorochroman-3-ylamine hydrochlorideHCID 11615490—
SolventEthyl AcetateHCID 8857—
ProductEtamicastat HCl saltHCID 10450386—

Reaction Steps

A stirred mixture of (R)-6,8-difluorochroman-3-ylamine hydrochloride (1.68 g, 7.58 mmol), [4-(tert-butyldimethylsilanyloxy)-3-oxobutyl]carbamic acid tert-butyl ester (3.13 g, 9.85 mmol), potassium thiocyanate (0.96 g, 9.85 mmol), water (0.18 mL, 10 mmol) and acetic acid (3.0 mL, 50 mmol) in ethyl acetate (30 mL) was refluxed for 7 hours, cooled to room temperature, washed by sodium bicarbonate solution, dried over anhydrous magnesium sulphate and evaporated in vacuo. The residue was purified by column chromatography on silica using ethyl acetate—petroleum ether mixture as eluent. The resulting oil (2.15 g) was dissolved in ethyl acetate (20 ml), 2M HCl solution in ethyl acetate was added (20 mL, 40 mmol) and the mixture was stirred for 2 hours at room temperature. The precipitate was removed by filtration and washed with ethyl acetate to give crystals, which decomposed without melting.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259271B2
Source datasetuspto-grants-2007_08
ORD IDord-df33cdcc8d434ef1ad1a31d36688c222
Source noteuspto-grants-2007_08