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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876044Generated: November 1, 2026

Cesium carbonate → HCID 59286618, compound

https://huagongshe.com/reaction/1876044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantCarbonimidodithioic acid, N-[6-(4-methyl-1H-imidazol-1-yl)-4-pyrimidinyl]-, dimethyl esterHCID 59286669—
Reactant(S)-3-(aminomethyl)quinuclidin-3-ol dihydrochlorideHCID 66724709—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductAmmonium hydroxide methanolHCID 21894508—
ProductHCID 59286618HCID 59286618154.5%

Reaction Steps

A suspension of (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride (412 mg, 1.80 mmol), dimethyl 6-(4-methyl-1H-imidazol-1-yl)pyrimidin-4-ylcarbonimidodithioate (419 mg, 1.5 mmol), and cesium carbonate (1.22 g, 3.75 mmol) was stirred in DMF (3.8 mL) at 75° C. for 2 h. The reaction was concentrated and purified by flash chromatography on a 40 g silica gel cartridge with a pre-run of 1% [95:5 MeOH/NH4OH] in EtOAc, then 1 to 2% [95:5 MeOH/NH4OH] in CHCl3 to yield (R)—N-(6-(4-methyl-1H-imidazol-1-yl)pyrimidin-4-yl)-4H-1′-azaspiro[oxazole-5,3′-bicyclo[2.2.2]octan]-2-amine (472 mg, 92% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 9.40 (1H, br. s.), 8.56 (1H, d, J=1.01 Hz), 8.28 (1H, d, J=1.26 Hz), 7.21 (1H, s), 6.76 (1H, br. s.), 3.97 (1H, d, J=9.57 Hz), 3.63 (1H, d, J=9.57 Hz), 3.33 (1H, dd, J=14.86, 1.76 Hz), 2.62-3.05 (5H, m), 2.24 (3H, d, J=1.01 Hz), 2.03-2.19 (2H, m), 1.65-1.81 (1H, m), 1.39-1.62 (2H, m). LCMS: RT=0.25, 0.46 min, MH+=340.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309577B2
Source datasetuspto-grants-2012_11
ORD IDord-6f365e2f936049439ce2b7fcf1179b2b
Source noteuspto-grants-2012_11