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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18086생성일: 2026년 10월 25일

tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylate → (S)-2-[(6,7-Difluoroquinoxalin-2-ylamino)methyl]-piperidine-1-carboxylic acid tert buty ester

https://huagongshe.com/reaction/18086

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
반응물2-Chloro-6,7-difluoroquinoxalineHCID 10375543—
용매DimethylformamideHCID 6228—
생성물(S)-2-[(6,7-Difluoroquinoxalin-2-ylamino)methyl]-piperidine-1-carboxylic acid tert buty esterHCID 69980785—

반응 조건

온도90 °C

반응 단계

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (0.607 g), and 2-chloro-6,7-difluoroquinoxaline McQuaid et. al. J. Med. Chem. (1992), 35(18), 3319-24 (0.569 g) were dissolved in dimethylformamide (1 ml) and heated to 90° C. for 5 days under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 10 to 50% ethyl acetate in hexane. The title compound was obtained as a pale yellow solid (0.460 g), MH+ 379.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741329B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a91e682d1e5f4f50b13ded6fe34a9d27
출처 메모uspto-grants-2010_06