戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 724729作成日:2026年10月26日

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

https://huagongshe.com/reaction/724729

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物TriethylamineHCID 8471—
反応物4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 197747—
反応物2,3-dimethyl-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1H-imidazol-3-ium trifluoromethanesulfonateHCID 10872832—
溶媒WaterHCID 962—
生成物4-(4-Fluorophenyl)-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1,2,3,6-tetrahydropyridineHCID 2187868552%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141596B2
出典データセットuspto-grants-2006_11
ORD IDord-43b866aa4e534fa891134f373c1754f0
出典メモuspto-grants-2006_11