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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523563Generated: November 3, 2026

Pyridine → (S)-N-(3-(2,6-dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/1523563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsothiocyanatosodiumHCID 10953423—
Reactant3-(2,6-Dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-amineHCID 67486800—
Reactant(R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chlorideHCID 86644147—
SolventAcetonitrileHCID 6342—
Product(S)-N-(3-(2,6-dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amineHCID 6748634542%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of sodium isothiocyanate (0.24 g, 3.0 mmol) in acetonitrile (30 mL) was added pyridine (0.51 g, 6.5 mmol) followed by (R)—N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (0.77 g, 2.6 mmol) and the reaction was stirred at 60° C. for 20 minutes, followed by addition of 3-(2,6-dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-amine (0.70 g, 2.2 mmol) and the reaction was stirred overnight at 60° C. The reaction was concentrated in vacuo and the residue partitioned between EtOAc and 2 M NaOH. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo. The material was purified over silica gel (30% EtOAc in CH2Cl2) to afford (S)—N-(3-(2,6-dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine (0.50 g, 0.91 mmol, 42% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079890B2
Source datasetuspto-grants-2015_07
ORD IDord-8f4677c1f9ba4fb69e70dc46439d64a0
Source noteuspto-grants-2015_07