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HRID 38761作成日:2026年10月26日

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

https://huagongshe.com/reaction/38761

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物Exo-2-bornanamineHCID 98480—
反応物Ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 58168829—
溶媒WaterHCID 962—
生成物ethyl rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylateHCID 6672002684.4%

反応手順

To a mixture of ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate (500 mg) and 1,4-dioxane (10 mL) was added exo-2-aminonorbornane (612 mg) at room temperature, and the mixture was stirred at the same temperature for 2 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 rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate (470 mg) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524727B2
出典データセットuspto-grants-2013_09
ORD IDord-b5b7b63357704bcca1194abd21b4cdbd
出典メモuspto-grants-2013_09