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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352958생성일: 2026년 10월 27일

Ethanol → 4-[(6-Chloronaphthalen-2-yl)sulfonyl]-1-[(6-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]piperazine-2-carboxylic Acid

https://huagongshe.com/reaction/352958

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물4-[(6-Chloronaphthalen-2-yl)sulfonyl]-2-(ethoxycarbonyl)-1-[(6-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]piperazineHCID 22710002—
용매TetrahydrofuranHCID 8028—
생성물4-[(6-Chloronaphthalen-2-yl)sulfonyl]-1-[(6-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]piperazine-2-carboxylic AcidHCID 22710353—

반응 단계

In tetrahydrofuran (10 ml), 4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-(ethoxycarbonyl)-1-[(6-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]piperazine (2.08 g) was dissolved, followed by the addition of ethanol (20 ml) and a 1N aqueous solution (3.70 ml) of sodium hydroxide. The resulting mixture was stirred at room temperature for 1 hour. After concentration of the reaction mixture under reduced pressure, the residue was added with water (20 ml). The precipitate thus formed was collected by filtration, whereby the title compound (1.39 g) was obtained as a pale yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06747023B1
출처 데이터셋uspto-grants-2004_06
ORD IDord-90f2c4195fba489180b31f4618eb5a99
출처 메모uspto-grants-2004_06