戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 228028作成日:2026年10月26日

4-(Piperidin-1-yl)aniline → (2S,4S)-4-fluoro-1-[[N-[4-[N-(4-piperidinylphenyl)amino]carbonylbicyclo[2.2.2]oct-1-yl]amino]acetyl]pyrrolidine-2-carbonitrile

https://huagongshe.com/reaction/228028

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Piperidin-1-yl)anilineHCID 413501—
反応物(2S,4S)-1-[[N-(4-carboxybicyclo[2,2,2]oct-1-yl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrileHCID 57634365—
生成物(2S,4S)-4-fluoro-1-[[N-[4-[N-(4-piperidinylphenyl)amino]carbonylbicyclo[2.2.2]oct-1-yl]amino]acetyl]pyrrolidine-2-carbonitrileHCID 5775685719.6%

反応手順

In a similar manner to Example 63, (2S,4S)-1-[[N-(4-carboxybicyclo[2.2.2]oct-1-yl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile (50.0 mg) and N-(4-aminophenyl)piperidine (61.4 mg) were used to obtain (2S,4S)-4-fluoro-1-[[N-[4-[N-(4-piperidinylphenyl)amino]carbonylbicyclo[2.2.2]oct-1-yl]amino]acetyl]pyrrolidine-2-carbonitrile (14.6 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560569B2
出典データセットuspto-grants-2009_07
ORD IDord-0e990551bf114d7fa04613718aa3609e
出典メモuspto-grants-2009_07