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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352851생성일: 2026년 10월 26일

Triethylamine → 1-[(6-tert-Butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine

https://huagongshe.com/reaction/352851

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PyBOPHCID 2724699—
반응물6-Boc-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-carboxylic acidHCID 22709449—
반응물1-[(6-Chloronaphthalen-2-yl)sulfonyl]-3-ethoxycarbonylpiperazine hydrochlorideHCID 22710075—
용매DimethylformamideHCID 6228—
생성물1-[(6-tert-Butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-4-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazineHCID 22709517—

반응 단계

In N,N-dimethylformamide (30 ml), 6-tert-butoxycarbonyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid (WO94/21599) (742 mg), 1-[(6-chloronaphthalen-2-yl)sulfonyl]-3-ethoxycarbonylpiperazine hydrochloride (WO96/10022) (1.00 g) and benzotriazol-1-yloxy-tris(pyrrolidino)phosphonium hexafluorophosphate (PyBOP®) (1.50 g) were dissolved. Triethylamine (0.40 ml) was added to the resulting solution, followed by stirring overnight at room temperature. After the reaction mixture was concentrated under reduced pressure, ethyl acetate was added to the residue. The resulting mixture was washed with water and saturated aqueous NaCl solution and then, dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane ethyl acetate=4:1), whereby the title compound (505 mg, 30%) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06747023B1
출처 데이터셋uspto-grants-2004_06
ORD IDord-93559d8da7be42c5ae2bb390dae84e41
출처 메모uspto-grants-2004_06