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HRID 13156作成日:2026年10月26日

Water → 1-(4-chlorophenyl)-5-iodo-1H-indazole

https://huagongshe.com/reaction/13156

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium carbonateHCID 10796—
反応物Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
反応物2-Fluoro-5-iodobenzaldehydeHCID 16217058—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物1-(4-chlorophenyl)-5-iodo-1H-indazoleHCID 59339754—

反応手順

4-chlorophenylhydrazine hydrochloride (5.24 g, 29.27 mmol), 2-fluoro-5-iodobenzaldehyde (7.5 g, 30.00 mmol) and cesium carbonate (22.8 g, 69.98 mmol) was suspended in NMP (120 mL) and stirred at ambient temperature for 45 min. The temperature was raised to +160° C. and the reaction mixture was stirred for 1 h, the now black suspension was allowed to reach r.t. Water was added, the slurry was extracted with EtOAc (500 mL. The organic phase was washed with brine (2×). The brine fractions and waterphase was combined and backextracted once with EtOAc. This second EtOAc phase was washed with brine (2×) before combined with the previous EtOAc phase. The organic phases were dried over Na2SO4, filtered and evaporated. The black residue were dissolved in DCM/Heptane (=1/1) and filtered through a silica column, and the column was then further eluted with DCM/Heptane (=1/1) solvent mixture. The fractions containing product was evaporated, residue was dissolved in EtOAc and Heptane was added, evaporation and diluting with Heptane afforded a slurry, the solid material was collected by filtration and washed with Heptane. Yield 2.82 g (27%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728030B2
出典データセットuspto-grants-2010_06
ORD IDord-7aa4926ed1224a53859f2146651fd925
出典メモuspto-grants-2010_06