Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38762Generated: October 29, 2026

1,4-Dioxane → ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/38762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 58168829—
Reactantexo-Bicyclo[2.2.1]heptan-2-amine hydrochlorideHCID 66720410—
SolventWaterHCID 962—
Productethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylateHCID 6672022493.6%

Reaction Steps

To a mixture of ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate (400 mg), (1S,2S,4R)-bicyclo[2.2.1]heptan-2-aminehydrochloride (347 mg), and 1,4-dioxane (8 mL) was added N,N-diisopropyl ethylamine (1 mL) at room temperature, followed by stirring at the same temperature for 16 hours. To the reaction mixture was added water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate (417 mg) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524727B2
Source datasetuspto-grants-2013_09
ORD IDord-7b364c9ee82940c7b984d470e17e8512
Source noteuspto-grants-2013_09