HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882072Generated: November 1, 2026
Hydrochloric Acid → HCID 178503159, compound
https://huagongshe.com/reaction/1882072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59331349 | HCID 59331349 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178503159 | HCID 178503159 | 84.1% |
Reaction Steps
To a solution of 1-[3-chloro-4-(methylsulfanyl)phenyl]-1-(4-iodo-2-(pyridin-2-yl)-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazol-5-yl)-2-(tetrahydro-2H-pyran-4-yl)ethanol (0.520 g) in ethanol (10 mL) was added 3M hydrochloric acid (10 mL), and the mixture was stirred at 80° C. for 1.5 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-60:40, volume ratio) to give the title compound (0.343 g, yield 84%) as a colorless oil. MS: 358 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318746B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-29e02711b2464dcd8d9a3e86cf253e1b |
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| Source note | uspto-grants-2012_11 |
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