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HRID 905843作成日:2026年10月27日

Piperidine → acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester

https://huagongshe.com/reaction/905843

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物2-Acetoxyisobutyroyl chlorideHCID 123496—
反応物6-Amino-5-fluoroindolin-2-oneHCID 10103504—
溶媒TetrahydrofuranHCID 8028—
生成物acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl esterHCID 5925010099.5%

反応条件

温度-40 °C

反応手順

A stirred solution of 5-fluoro-6-amino-1,3-dihydro-indol-2-one (410 mg, 2.46 mmol) in 10 ml of tetrahydrofuran was added with piperidine (0.3 ml). The mixture was cooled to −40° C. in an acetone-dry ice bath and added with acetic acid 1-chlorocarbonyl-1-methyl-ethyl ester (405 mg, 2.46 mmol) in 10 ml of tetrahydrofuran dropwise. Upon the completion of the addition, the resulting mixture was stirred at the room temperature overnight until the precipitate was formed. The solid was filtered, washed with water and recrystallized from methanol to give acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester (720 mg, 99.5%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08012966B2
出典データセットuspto-grants-2011_09
ORD IDord-032d03c0b0ae423ba66aa3e635e8c7b4
出典メモuspto-grants-2011_09