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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854700Generated: November 3, 2026

Acetic Acid → (R)-5-aminomethyl-1-(6,8-difluorochroman-3-yl)-1,3-dihydroimidazole-2-thione hydrochloride

https://huagongshe.com/reaction/854700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium thiocyanateHCID 516872—
Reactant(R)-6,8-difluorochroman-3-ylamine hydrochlorideHCID 11615490—
Reactanttert-Butyl (3-((tert-butyldimethylsilyl)oxy)-2-oxopropyl)carbamateHCID 11709260—
SolventEthyl AcetateHCID 8857—
Product(R)-5-aminomethyl-1-(6,8-difluorochroman-3-yl)-1,3-dihydroimidazole-2-thione hydrochlorideHCID 11695681—

Reaction Steps

A stirred mixture of (R)-6,8-difluorochroman-3-ylamine hydrochloride (0.22 g, 1.0 mmol), [3-(tert-butyldimethylsilanyloxy)-2-oxopropyl]carbamic acid tert-butyl ester (0.33 g, 1.1 mmol), potassium thiocyanate (0.11 g, 1.1 mmol) and acetic acid (0.3 mL, 5.0 mmol) in ethyl acetate (3 mL) was refluxed for 2 hours, cooled to room temperature, then washed by sodium bicarbonate solution, dried over anhydrous magnesium sulphate and evaporated in vacuo. The residue was purified by the column chromatography over silica gel using ethyl acetate—petroleum ether mixture as eluent. The resulting oil (0.23 g) was dissolved in ethyl acetate (2 ml), whereupon 2M HCl solution in ethyl acetate was added (2 mL, 4 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 of m.p. 192° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259271B2
Source datasetuspto-grants-2007_08
ORD IDord-a32d9e5e9645405d8259c3c01d3265f0
Source noteuspto-grants-2007_08