HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534066Generated: October 30, 2026
Hydrochloric Acid → HCID 68479286, compound
https://huagongshe.com/reaction/534066
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67486618 | HCID 67486618 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68479286 | HCID 68479286 | 77.6% |
Reaction Steps
(S)-N-(3-(2-methylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(2,2,5,5-tetramethyl-1,3-dioxolane-4-yl)-1,2,4-thiadiazol-5-amine (145 mg, 0.2774 mmol) was dissolved in EtOH (5 mL), and 6M HCl (0.3 mL) was added. The reaction was stirred at ambient temperature for 2 hours and then at 70° C. for 2 hours. The reaction was cooled to ambient temperature and partitioned between CH2Cl2 and saturated aqueous sodium bicarbonate. The organic layer was dried, filtered, concentrated and purified over silica gel (10% methanol in EtOAc) to afford (S)-2-methyl-1-(5-(3-(2-methylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)propane-1,2-diol hydrochloride (111.7 mg, 0.215 mmol, 77.6% yield) as a pale yellow solid after HCl salt formation. Mass Spectrum (apci) m/z=465.2 (M+H−HCl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853409B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-b0775fbbd3ae40f78501bad4b8968a94 |
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| Source note | uspto-grants-2014_10 |
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