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HRID 538085作成日:2026年10月25日

Water → 2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester

https://huagongshe.com/reaction/538085

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
反応物1-(Naphthalene-2-sulfonyl)-piperazineHCID 703957—
溶媒TetrahydrofuranHCID 8028—
生成物2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl esterHCID 5884497784%

反応手順

NaH 60% (0.0217 mol) was added portionwise at room temperature to a solution of 1-(2-naphtalenesulfonyl)-piperazine (0.011 mol) in THF (50 ml) under N2 flow. The mixture was stirred at room temperature for 1 hour, then cooled to 0° C. A solution of 2-(methylsulfonyl)-5-pyrimidinecarboxylic acid, ethyl ester (0.014 mol) in THF (30 ml) was added quickly. The mixture was stirred at room temperature for 2 hours, poured out into water and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue was taken up in diethyl ether. The precipitate was filtered off and dried, yielding 3.92 g (84%) of 2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester (interm. 8), melting point>260° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865720B2
出典データセットuspto-grants-2014_10
ORD IDord-04ddf9950e6b470aa8729598a55cb8aa
出典メモuspto-grants-2014_10