HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245770Generated: November 2, 2026
Acetic Acid → (R)-5-aminomethyl-1-(6,8-difluorochroman-3-yl)-1,3-dihydroimidazole-2-thione hydrochloride
https://huagongshe.com/reaction/1245770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | (R)-6,8-difluorochroman-3-ylamine hydrochloride | HCID 11615490 | — |
| Reactant | tert-Butyl (3-((tert-butyldimethylsilyl)oxy)-2-oxopropyl)carbamate | HCID 11709260 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-5-aminomethyl-1-(6,8-difluorochroman-3-yl)-1,3-dihydroimidazole-2-thione hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125904B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-8d7adbc33b5942e28c266b2a90564c6d |
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| Source note | uspto-grants-2006_10 |
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