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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29049생성일: 2026년 10월 25일

p-Toluenesulfonic acid → 4-(2-(4-Fluorophenyl)-1H-pyrrol-1-yl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/29049

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-amino-N-methylbenzene-1-sulfonamideHCID 74368—
반응물3-(5,5-Dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-oneHCID 10635463—
용매TolueneHCID 1140—
생성물4-(2-(4-Fluorophenyl)-1H-pyrrol-1-yl)-N-methylbenzenesulfonamideHCID 1052044740%

반응 단계

A mixture of 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-one (Step 4) (400 mg, 1.5 mmol), 4-[(N-methylamino)sulfonyl]aniline (Step 6) (308 mg, 1.65 mmol) and p-toluenesulfonic acid (40 mg) in toluene (80 ml) was heated to reflux for 48 hr. The reaction mixture was cooled, filtered and concentrated. The crude yellowish solid (760 mg) was chromatographed (silica gel, hexane/ethyl acetate 7/3) to give 4-[2-(4-fluorophenyl)-1H-pyrrol-1-yl]-N-methylbenzenesulfonamide (198 mg, 40%) as a white solid: mp (DSC) 174° C. Anal Calc'd. for C17H15N2FO2S 0.25 H2O: C, 60.97; H, 4.67; N, 8.37. Found: C, 60.86; H, 4.56; N, 8.01.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420061B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-e856ec518eca4dabaf48ed51495e8a8b
출처 메모uspto-grants-2008_09