戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1960445作成日:2026年10月26日

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

https://huagongshe.com/reaction/1960445

反応式

関与物質

役割名称HCID仕込み量
反応物1-Tert-butyl 2-ethyl 7-[cyclopropyl(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)indoline-1,2-dicarboxylateHCID 59136016—
溶媒Hydrogen chloride-ethyl acetateHCID 21866389—
生成物Ethyl 7-[cyclopropyl(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)indoline-2-carboxylateHCID 5913605796%

反応手順

1-tert-Butyl 2-ethyl 7-[cyclopropyl(pyridin-2-ylsulfonyl)amino]-5-(2-methoxyethoxy)indoline-1,2-dicarboxylate (1.70 g) was added to 4N hydogen chloride-ethyl acetate solution (50 mL), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to give the title compound (1.34 g, yield 96%) as a pale-yellow amorphous solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08410087B2
出典データセットuspto-grants-2013_04
ORD IDord-55858cb968b441629aeb84d44fdd1110
出典メモuspto-grants-2013_04