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HRID 967378作成日:2026年10月26日

tert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylate → 1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/967378

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylateHCID 67472855—
溶媒Diethyl EtherHCID 3283—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-oneHCID 2761152150.4%

反応手順

4-(2-Oxo-2,3-dihydro-indol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (3.9 g, 12.3 mmol) was set stirring in 30 mL of 1:1 TFA/CH2Cl2. After 45 min the solvent was evaporated under reduced pressure to give a clear purple oil. The oil was brought up in diethyl ether and cooled on ice to give a precipitate. The solid was filtered, washed with ether and air dried to give 4.0 g (100%) of the title compound as a TFA salt. 1H NMR (400 MHz, DMSO-d6): 8.6 (br s, 1H), 7.27 (m, 3H), 7.03 (m, 1H), 4.45 (m, 1H), 3.56 (s, 2H), 3.42 (m, 2H), 3.09 (m, 2H), 2.53 (m, 2H), 1.78 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06953793B2
出典データセットuspto-grants-2005_10
ORD IDord-cd46555bdbc345a792d754d91f1b4e37
出典メモuspto-grants-2005_10