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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724729생성일: 2026년 10월 25일

Acetonitrile → 4-(4-Fluorophenyl)-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/724729

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 197747—
반응물2,3-dimethyl-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1H-imidazol-3-ium trifluoromethanesulfonateHCID 10872832—
용매WaterHCID 962—
생성물4-(4-Fluorophenyl)-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1,2,3,6-tetrahydropyridineHCID 2187868552%

반응 단계

A solution of 4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochloride (150 mg, 700 μmol), 2,3-dimethyl-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1H-imidazol-3-ium trifluoromethanesulfonate (410 mg, 1.05 mmol), acetonitrile (5 mL) and triethylamine (98 μL, 700 μmol) was stirred at 25° C. for 24 h. The reaction was diluted with water and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by preparative LCMS to yield the desired product (117 mg, 52%). MF=C15H16FN3O2S; LCMS found for C15H17FN3O2S(M+H)+: m/z=322.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141596B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-43b866aa4e534fa891134f373c1754f0
출처 메모uspto-grants-2006_11