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HRID 1532579作成日:2026年10月25日

Iodine → 3-(3-Fluoro-5-chloro-2-pyridyl)-4-iodo-5-difluoromethoxy-1-methyl-[1H]-pyrazole

https://huagongshe.com/reaction/1532579

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物3-(3-fluoro-5chloro-2-pyridyl)-5-difluoromethoxy-1-methyl-[1H]-pyrazoleHCID 21712132—
触媒Silver nitriteHCID 160904—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物3-(3-Fluoro-5-chloro-2-pyridyl)-4-iodo-5-difluoromethoxy-1-methyl-[1H]-pyrazoleHCID 2201357991%

反応条件

温度22 °C

反応手順

3.0 g of 3-(3-fluoro-5-chloro-2-pyridyl)-5-difluoromethoxy-1-methyl-[1H]-pyrazole (Example H15) are dissolved in 30 ml of methylene chloride, and 1.83 g of silver(I) nitrite and 3.02 g of iodine are then added. The mixture is stirred overnight at 22° C. It is then diluted with diethyl ether and extracted successively with aqueous sodium metabisulfite solution and brine. After drying of the organic phase over sodium sulfate and filtration, the filtrate is concentrated in vacuo together with twice the amount of silica gel. After application of this silica gel to a flash column, the column is eluted with n-hexane/ethyl acetate (3/1). 3.97 g of the desired title compound are obtained as a beige solid of melting point 77-78° C. in this manner.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06204221B1
出典データセットuspto-grants-2001_03
ORD IDord-30c05a42368142c3b41bdb27ae10dfb3
出典メモuspto-grants-2001_03