Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523644Generated: November 3, 2026

Hydrochloric Acid → HCID 68476202, compound

https://huagongshe.com/reaction/1523644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 67487814HCID 67487814—
SolventEthanolHCID 702—
ProductHCID 68476202HCID 6847620264.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

N-(3-(2-ethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-((2S,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine (1.6 g, 2.70 mmol) was dissolved in EtOH (30 mL) and 4N HCl (1 mL) added and heated to 50° C. overnight. Additional 4N HCl was added (1 mL) and heated for 4 hours. The reaction was cooled to ambient temperature, partitioned between CH2Cl2 and saturated aqueous sodium bicarbonate, extracted with CH2Cl2, dried over sodium sulfate, filtered and concentrated. The residue was purified over silica gel (10% methanol in EtOAc) to afford (1S,2S)-1-(5-(3-(2-ethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)-3-methoxypropane-1,2-diol hydrochloride (0.957 g, 1.74 mmol, 64.6% yield) as a tan solid after HCl salt formation. Mass Spectrum (apci) m/z=513.1 (M+H−HCl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079890B2
Source datasetuspto-grants-2015_07
ORD IDord-7e52385291de474c948dd54dd4ef1f3b
Source noteuspto-grants-2015_07