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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178962생성일: 2026년 10월 27일

Piperidine → N-(4-Fluoro-benzyl)-4-(3-piperidin-1-yl-indazole-1-sulfonyl)-benzamide

https://huagongshe.com/reaction/1178962

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamideHCID 58975152—
용매Ethyl AcetateHCID 8857—
생성물N-(4-Fluoro-benzyl)-4-(3-piperidin-1-yl-indazole-1-sulfonyl)-benzamideHCID 589751997%

반응 조건

온도90 °C

반응 단계

Dissolve 4-(3-chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide (91 mg, 0.20 mmol) in piperidine (1.0 mL) and stir at 90° C. overnight. Dilute the solution with EtOAc (30 mL) and wash with 1N HCl (15 mL) and satd NaHCO3 (15 mL). Dry, filter and concentrate the organic solution and purify the residue by flash chromatography, using a linear gradient of 100% hexanes to 50% EtOAc/hexanes, to give the title compound as a light yellow foam (7 mg, 7%). MS (ES) 493.0 (M+1)+, 491.2 (M−1)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276516B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-a411de95c50a48069dbdc62f1f3a907b
출처 메모uspto-grants-2007_10