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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279352생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/279352

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물delta-Oxobenzenepentanoic acidHCID 73914—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 18426239—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물1-(4-Chlorobenzyl)-3-[(4-benzoylbutyryl)amino]homopiperidineHCID 9823008—

반응 조건

온도25 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-e90615f838734037a6c71d400c1016f1
출처 메모uspto-grants-2002_03