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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533997Generated: October 28, 2026

Pyridine → 1,4-Dioxaspiro[4.5]decan-2-yl-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/533997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium thiocyanateHCID 516871—
Reactant5-Bromo-3-(2-methylpyridin-3-yloxy)pyridin-2-amineHCID 67486181—
Reactant(R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chlorideHCID 86644147—
SolventAcetonitrileHCID 6342—
Product1,4-Dioxaspiro[4.5]decan-2-yl-1,2,4-thiadiazol-5-amineHCID 8664414950%

Reaction Conditions

Temperature40 °C

Reaction Steps

(R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (1.86 g, 6.25 mmol), pyridine (1.13 g, 14.3 mmol) and sodium thiocyanate (0.58 g, 7.14 mmol) were dissolved in acetonitrile (45 mL). The solution was heated to 40° C. for 40 minutes. 5-bromo-3-(2-methylpyridin-3-yloxy)pyridin-2-amine (1.0 g, 3.57 mmol) was added and the reaction was heated at 60° C. overnight. The solution was cooled to 0° C., filtered and the solid was dried to give (S)-N-5-bromo-3-(2-methylpyridin-3-yloxy)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine (0.90 g, 1.78 mmol, 50% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-1558b255c35d429d82a05b1c51d93cad
Source noteuspto-grants-2014_10