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HRID 612486作成日:2026年10月25日

Dimethylcarbamoyl Chloride → 2,3-Dihydro-4-fluoro-2-(4-pyridinylamino)-1H-isoindol-5-yl dimethylcarbamate hydrochloride

https://huagongshe.com/reaction/612486

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethylcarbamoyl ChlorideHCID 6598—
反応物TriethylamineHCID 8471—
反応物Sodium BicarbonateHCID 516892—
反応物2,3-dihydro-4-fluoro-2-(4-pyridinylamino)-1H-isoindol-5-ol hydrobromideHCID 19595201—
溶媒ChloroformHCID 6212—
生成物2,3-Dihydro-4-fluoro-2-(4-pyridinylamino)-1H-isoindol-5-yl dimethylcarbamate hydrochlorideHCID 1959520269.3%

反応手順

To a mixture of 2,3-dihydro-4-fluoro-2-(4-pyridinylamino)-1H-isoindol-5-ol hydrobromide (600 mg), triethylamine (614 mg), and chloroform (10 ml), dimethylcarbamyl chloride (237 mg) in chloroform (5 ml) was added dropwise, with stirring at ambient temperature, under nitrogen. The reaction mixture was stirred under reflux for 5 hrs, at ambient temperature overnight and poured into dilute sodium bicarbonate solution (100 ml). The layers were separated. The aqueous phase was extracted with chloroform, and the combined organic layers were dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated in vacuo. The residue was flash chromatographed (silica), eluting with 7% methanol-dichloromethane followed by 185:14:1 dichloromethane-methanol-ammonium hydroxide. The appropriate fractions were collected and evaporated. The residue was dissolved in absolute ethanol and excess ethereal hydrogen chloride was added. Ether was added and the solution was cooled. The precipitate was collected to give 450 mg (69%) of product, mp 250-252° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06004977
出典データセットuspto-grants-1999_12
ORD IDord-84bb95d4e2c54ec2a49bf346cd8dcd44
出典メモuspto-grants-1999_12