돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1921444생성일: 2026년 10월 26일

4-Benzoylpiperidine hydrochloride → 5-[5-(4-Benzoylpiperidine-1-sulfonyl)thiophen-2-yl]-3-ethyl-6-methyl-1H-pyridin-2-one

https://huagongshe.com/reaction/1921444

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzoylpiperidine hydrochlorideHCID 2724437—
반응물5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chlorideHCID 86610352—
생성물5-[5-(4-Benzoylpiperidine-1-sulfonyl)thiophen-2-yl]-3-ethyl-6-methyl-1H-pyridin-2-oneHCID 5880859985%

반응 단계

5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with phenyl-piperidin-4-yl-methanone hydrochloride as described in Step 5, Example 24 to give the title compound as a yellow solid (85% yield). LC/MS: RT 3.27 min, m/e 471 (M+H); 1H NMR (CDCl3, δ, ppm): 11.95 (1H, s), 7.89 (2H, dd), 7.55-7.60 (1H, m), 7.44-7.52 (3H, m), 7.33 (1H, s), 7.01 (1H, d), 3.79-3.84 (2H, m), 3.27-3.36 (1H, m), 2.73-2.82 (2H, m), 2.60 (2H, q), 2.48 (3H, s), 1.89-2.05 (4H, m), 1.24 (3H, t).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173682B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-5d83e873278542a6882c7abaf8a3b2c4
출처 메모uspto-grants-2012_05