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HRID 1633719作成日:2026年10月26日

Ammonium Chloride → HCID 178526507、化合物

https://huagongshe.com/reaction/1633719

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物4-Iodo-1-tritylimidazoleHCID 618252—
反応物5-Nitro-3,4-dihydronaphthalen-1(2H)-oneHCID 10261946—
反応物HCID 178418443HCID 178418443—
溶媒DichloromethaneHCID 6344—
生成物HCID 178526507HCID 178526507—

反応手順

A solution of 4-iodo-1-trityl-1H-imidazole (5.5 g, 13 mmol) (prepared as described by Kirk, K. J. Heterocyclic Chem. (1985), 22, 57-59) in dichloromethane (50 mL) was treated with ethylmagnesium bromide (3.0 M in diethyl ether, 4.2 mL) over 4 minutes, stirred for 30 minutes, treated with 5-nitrotetralone (prepared as described by Zhang, M J. Amer. Chem. SoC, (1994), 116, 4852-4857), stirred for 6 hours, treated with ammonium chloride solution (50 mL) and extracted with a mixture of diethyl ether (300 mL) and ethyl acetate (50 mL). The organic layer was isolated, treated with dichloromethane (500 mL) to dissolve the product which started to crystallize, dried (MgSO4), filtered, concentrated, treated with trifluoroacetic acid (80 mL), stirred for 48 hours, concentrated to an oil, neutralized with sodium bicarbonate solution and extracted twice with dichloromethane. The combined dichloromethane layers were dried (MgSO4), filtered and concentrated. The residue was purified on silica gel with a gradient of 5%-10% methanol/dichloromethane to provide the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06503935B1
出典データセットuspto-grants-2003_01
ORD IDord-45768ce4f2fd4507887223018fed9d04
出典メモuspto-grants-2003_01