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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351543Generated: November 3, 2026

Carbon Dioxide → HCID 4742715, compound

https://huagongshe.com/reaction/2351543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHexahydro-2,5-methanopentalene-3a(1H)-carboxylic acidHCID 2733865—
ReactantHCID 14877867HCID 14877867—
SolventChloroformHCID 6212—
ProductHCID 4742715HCID 4742715—

Reaction Steps

To a stirred solution of hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid (1.0 g, 6.0×10-3 mol) in 25 ml of chloroform under a dry nitrogen atmosphere, was added carbonyldiimidazole (0.98 g, 6.0×10-3 mol). The resulting solution was stirred at ambient temperature for three hours, during which time a gas (CO2) was evolved. A solution of 2-[1-(2-pyrimidyl)-4-piperazinyl]ethanol (1.25 g, 6.0×10-3 mol) in 25 ml of chloroform was then added, and the resulting reaction mixture was stirred under nitrogen at ambient temperature for two days. The mixture was diluted to 150 ml with chloroform, washed with three-one hundred ml portions of water, dried over anhydrous sodium sulfate, and concentrated on a rotary evaporator. The desired product (TLC on silica using a 30% methanol in ethyl acetate solvent system, Rf=0.45) was isolated by gravity chromatography on silica gel and converted to the hydrochloride salt with isopropanolic HCl (1.76 g, 61% yield), mp.=219°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873331
Source datasetuspto-grants-1989_10
ORD IDord-b92506b9c4b047949b9cc0fbf651784c
Source noteuspto-grants-1989_10