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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538085생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/538085

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
반응물1-(Naphthalene-2-sulfonyl)-piperazineHCID 703957—
용매TetrahydrofuranHCID 8028—
생성물2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl esterHCID 5884497784%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865720B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-04ddf9950e6b470aa8729598a55cb8aa
출처 메모uspto-grants-2014_10