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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523671Generated: November 3, 2026

Pyridine → HCID 67485959, compound

https://huagongshe.com/reaction/1523671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium thiocyanateHCID 516871—
ReactantHCID 67486353HCID 67486353—
Reactant(R)-N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chlorideHCID 86644147—
SolventAcetonitrileHCID 6342—
ProductHCID 67485959HCID 6748595992.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

A flask was charged with (R)—N-(methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (1.53 g, 5.15 mmol), pyridine (1.25 ml, 15.4 mmol), sodium thiocyanate (0.417 g, 5.15 mmol) and acetonitrile (15 mL). The solution was heated to 40° C. for 40 minutes. 5-Bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)pyridin-2-amine (1.02 g, 3.43 mmol) was added and the reaction was heated to 70° C. overnight. The reaction was cooled to ambient temperature, partitioned between EtOAc and water, dried over sodium sulfate, filtered and concentrated. The residue was purified over silica gel (10% MeOH/EtOAc) to afford (S)—N-(5-bromo-3-(1,3,5-trimethyl-1H-pyrazo 1-4-yloxy)pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decan-2-yl)-1,2,4-thiadiazol-5-amine (1.66 g, 3.18 mmol, 92.7% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079890B2
Source datasetuspto-grants-2015_07
ORD IDord-7e65d5958ed447ff8db99529902d46fb
Source noteuspto-grants-2015_07