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HRID 279352作成日:2026年10月26日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-(4-Chlorobenzyl)-3-[(4-benzoylbutyryl)amino]homopiperidine

https://huagongshe.com/reaction/279352

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物delta-Oxobenzenepentanoic acidHCID 73914—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 18426239—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物1-(4-Chlorobenzyl)-3-[(4-benzoylbutyryl)amino]homopiperidineHCID 9823008—

反応条件

温度25 °C

反応手順

A solution of 3-amino-1-(4-chlorobenzyl)homopiperidine (24 mg, 0.10 mmol) and 4-benzoylbutyric acid (1.2 equiv.) in CHCl3 (1 mL) was treated with EDCI (23 mg), HOBt (16.2 mg) and Et3N (15.2 μL), and stirred at 25° C. for 16 h. The reaction mixture was diluted with CH2Cl2 (0.5 mL), washed with 2 N aqueous NaOH solution (2×0.75 mL), dried by filtration through a PTFE membrane and concentrated to afford 1-(4-chlorobenzyl)-3-[(4-benzoylbutyryl)amino}homopiperidine (compound No. 994) (43 mg, 99%): The purity was determined by RPLC/MS (98%); ESI/MS m/e 413 (M++H, C24H29ClN2O2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362177B1
出典データセットuspto-grants-2002_03
ORD IDord-e90615f838734037a6c71d400c1016f1
出典メモuspto-grants-2002_03