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HRID 501437作成日:2026年10月25日

Hexachloroethane → 3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/501437

反応式

関与物質

役割名称HCID仕込み量
反応物HexachloroethaneHCID 6214—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium diisopropylamideHCID 2724682—
反応物3-(2-Butynyl)-4-chloro-3H-imidazo[4,5-c]pyridineHCID 23070729—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridineHCID 2307098021%

反応手順

2.22 ml of a tetrahydrofuran solution of lithium diisopropylamide was added dropwise to a 5 ml tetrahydrofuran solution of 490 mg of 3-(2-butynyl)-4-chloro-3H-imidazo[4,5-c]pyridine in a dry ice-methanol bath, and the mixture was stirred below −66° C. for 20 minutes. The resulting reaction mixture was added dropwise to a 2 ml tetrahydrofuran solution of 1.13 g of hexachloroethane while the temperature of the mixture was controlled to be −63° C. or lower. The mixture was stirred for one hour and 40 minutes in the same bath, and then a saturated aqueous ammonium chloride solution was added thereto. The resulting mixture was extracted twice with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, then filtered. The filtrate was concentrated under reduced pressure. Then, the resulting residue was purified by silica gel column chromatography. Thus, 120 mg of brown oily material was obtained from the fraction eluted with hexane-ethyl acetate (2:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772226B2
出典データセットuspto-grants-2010_08
ORD IDord-8adadceae381408d99ea7a971222e9dd
出典メモuspto-grants-2010_08