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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15724생성일: 2026년 10월 24일

4-Chlorobenzenesulfonyl chloride → 1,5-bis-(4-chloro-benzenesulfonyl)-6-phenyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/ko/reaction/15724

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzenesulfonyl chlorideHCID 7398—
반응물6-Phenyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl esterHCID 59342400—
용매Ethyl AcetateHCID 8857—
생성물1,5-bis-(4-chloro-benzenesulfonyl)-6-phenyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridineHCID 59342346—

반응 단계

Compound 52 from the previous step (1.1 g, 3.67 mmol) was dissolved in ethyl acetate (15 ml). HCl (g) was bubbled into the solution for 5 minutes. Solvent was removed under reduced pressure and the residue was re-dissolved in pyridine (15 ml). 4-chlorophenylsulfonyl chloride (1.55 g, 2.2 eq.) was added to the solution at zero degrees. The mixture was stirred at zero degrees and slowly raised to room temperature upon stirring overnight. Ethyl acetate (100 ml) was added to the reaction mixture, and the solution was washed with sat. NaHCO3 (2×25 ml), 10% HCl solution (2×25 ml) and brine (10 ml). Sample dried over (MgSO4), and solvent was removed under reduced pressure. The crude product was purified via flash chromatography, eluted with EtOAc/hexane (15:85) to give a white solid as the mixture of two regioisomers. LCMS 569.9 (M+23)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732609B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f296dfa423414303b11e9b4c72dcf515
출처 메모uspto-grants-2010_06