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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279324생성일: 2026년 10월 26일

Acetic Acid → 4-[{N-(2-amino-4,5-difluorobenzoyl)glycyl}aminomethyl]-1-(5-bromo-2-ethoxybenzyl)piperidine

https://huagongshe.com/reaction/279324

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물5-Bromo-2-ethoxybenzaldehydeHCID 144901—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-[[N-(2-(tert-butoxycarbonylamino)-4,5-difluorobenzoyl)glycyl]aminomethyl]piperidineHCID 18426202—
용매MethanolHCID 887—
생성물4-[{N-(2-amino-4,5-difluorobenzoyl)glycyl}aminomethyl]-1-(5-bromo-2-ethoxybenzyl)piperidineHCID 508910—

반응 조건

온도50 °C

반응 단계

To a mixture of 4-[{N-(2-(tert-butoxycarbonylamino)-4,5-difluorobenzoyl)glycyl}aminomethyl]piperidine (0.050 mmol), 5-bromo-2-ethoxybenzaldehyde (0.15 mmol), methanol (1.2 mL), and acetic acid (0.030 mL) was added NaBH3CN (0.25 mmol) in methanol (0.50 mL). The reaction mixture was stirred at 50° C. for 13 h. The mixture was cooled to room temperature, loaded onto Varian™ SCX column, and washed with CH3OH (5 mL×3). Product was eluted off using 2 N NH3 in CH3OH (5 mL) and concentrated. To the resulting material were added dichloromethane (1 mL) and trifluoroacetic acid (TFA) (0.50 mL) and the solution was stirred at room temperature for 10 min. The reaction mixture was concentrated, and the residue was dissolved in methanol, loaded onto Varian™ SCX column, and washed with CH3OH (5 mL×2). Product was eluted off using 2 N NH3 in CH3OH (5 mL) and concentrated. Preparative TLC (SiO2, ethyl acetate/methanol=10/1) gave 4-[{N-(2-amino-4,5-difluorobenzoyl)glycyl}aminomethyl]-1-(5-bromo-2-ethoxybenzyl)piperidine (Compound No. 2052) (10.2 mg, 38%): The purity was determined by RPLC/MS (96%); ESI/MS m/e 539.2 (M++H, C24H29BrF2N4O3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-b999fcc9697e417ea71b96dd66618cd6
출처 메모uspto-grants-2002_03