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HRID 1994878作成日:2026年10月27日

Pyridine-2-sulfonyl Chloride → 1-Tert-butyl 2-ethyl 7-[cyclopropyl(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)indoline-1,2-dicarboxylate

https://huagongshe.com/reaction/1994878

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine-2-sulfonyl ChlorideHCID 3787675—
反応物1-Tert-butyl 2-ethyl 7-(cyclopropylamino)-5-(2-methoxyethoxy)indoline-1,2-dicarboxylateHCID 59303509—
溶媒PyridineHCID 1049—
生成物1-Tert-butyl 2-ethyl 7-[cyclopropyl(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)indoline-1,2-dicarboxylateHCID 5913601667%

反応手順

To a mixture of 1-tert-butyl 2-ethyl 7-(cyclopropylamino)-5-(2-methoxyethoxy)indoline-1,2-dicarboxylate (1.9 g) and pyridine (3 mL) was added a mixture of 2-pyridylsulfonyl chloride (1.2 g) and pyridine (2 mL) at 0° C., and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate and water. The organic layer was washed with aqueous 10% aqueous citric acid solution, aqueous sodium bicarbonate solution and saturated brine, dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give the title compound (1.70 g, yield 67%) as a pale-yellow oil from a fraction eluted with ethyl acetate-hexane (9:1, volume ratio). MS: 562 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652133B2
出典データセットuspto-grants-2010_01
ORD IDord-8b9754651a974095957c155615349eab
出典メモuspto-grants-2010_01