HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511028Generated: November 2, 2026
Pyridine → 1,4-Dioxaspiro[4.5]decan-2-yl-1,2,4-thiadiazol-5-amine
https://huagongshe.com/reaction/1511028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Isothiocyanatosodium | HCID 10953423 | — |
| Reactant | 3-(2,6-Dimethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-amine | HCID 67486800 | — |
| Reactant | (R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride | HCID 86644147 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,4-Dioxaspiro[4.5]decan-2-yl-1,2,4-thiadiazol-5-amine | HCID 86644149 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08212045B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-68d6c0eb37d3477b80d021e8d8cec238 |
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| Source note | uspto-grants-2012_07 |
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