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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875949Generated: October 29, 2026

Cesium carbonate → (R)-N-(5-(methylthio)pyrazin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

https://huagongshe.com/reaction/1875949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant2-Isothiocyanato-5-(methylthio)pyrazineHCID 57476580—
Reactant(S)-3-(aminomethyl)quinuclidin-3-ol dihydrochlorideHCID 66724709—
SolventDimethylformamideHCID 6228—
Product(R)-N-(5-(methylthio)pyrazin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amineHCID 5808796016%

Reaction Steps

To (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride (0.375 g, 1.637 mmol) in N,N-dimethylformamide (15 mL) was added Cs2CO3 (1.333 g, 4.09 mmol) and 2-isothiocyanato-5-(methylthio)pyrazine (0.3 g, 1.637 mmol). The suspension was stirred at room temperature for 30 minutes. N,N′-diisopropylcarbodiimide (0.765 mL, 4.9 mmol) was then added and the mixture was continued to stir at room temperature for 18 hours. The mixture was concentrated and purified by silica gel chromatography (5-25% 9:1 methanol:ammonium hydroxide-ethyl acetate) to afford (R)—N-(5-(methylthio)pyrazin-2-yl)-4H-1′-azaspiro[oxazole-5,3′-bicyclo[2.2.2]octan]-2-amine (0.014 g, 0.04 mmol, 16% yield) as a yellow solid. M.P. 155-60° C. 1H NMR (400 MHz, MeOD) δ ppm 8.13 (1H, d), 8.06 (1H, s), 3.96 (1H, d), 3.66 (1H, d), 3.20 (1H, d), 3.08 (1H, d), 2.87-2.96 (2H, m), 2.72-2.82 (2H, m), 2.52 (3H, s), 2.00-2.19 (2H, m), 1.51-1.81 (3H, m). LCMS R.T.=1.01; [M+H]+=306.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309577B2
Source datasetuspto-grants-2012_11
ORD IDord-1842b38861aa4328bdfc04316b1ea5c6
Source noteuspto-grants-2012_11