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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133572생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → 2-((N-benzoylleucyl)aminomethyl)-1-(4-chlorobenzyl)pyrrolidine

https://huagongshe.com/reaction/133572

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Benzoyl-L-leucineHCID 853887—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidineHCID 14709036—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물2-((N-benzoylleucyl)aminomethyl)-1-(4-chlorobenzyl)pyrrolidineHCID 53639429—

반응 조건

온도25 °C

반응 단계

EDCl (23 mg), HOBt (16.2 mg) and triethylamine (15.2 μL) were added to a chloroform (1 mL) solution of 2-(aminomethyl)-1-(4-chlorobenzyl)pyrrolidine (22.5 mg, 0.10 mmol) and dl-benzoylleucine (0.12 mL), and the resulting mixture was stirred at 25° C. for 16 hours. The reaction mixture was diluted with dichloromethane (0.5 mL), washed with a 2 M aqueous solution of NaOH (0.75 mL×2), filtered through a PTFE membrane, thereby dried and concentrated to provide 2-[(N-benzoylleucyl)aminomethyl]-1-(4-chlorobenzyl)pyrrolidine (Compd. No. 344) (74 mg, quantitative). The purity was determined by RPLC/MS (85%). ESI/MS m/e 442 (M++H, C23H32ClN3O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390830B1
출처 데이터셋uspto-grants-2008_06
ORD IDord-a7466de645af45ffb3bc6e7d7e745a01
출처 메모uspto-grants-2008_06