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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18103생성일: 2026년 10월 25일

Diisopropylethylamine → (S)-2-[(4-Cyano-2,6-difluorophenylamino)-methyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/18103

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3,4,5-TrifluorobenzonitrileHCID 593814—
반응물tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
용매O-XyleneHCID 7237—
생성물(S)-2-[(4-Cyano-2,6-difluorophenylamino)-methyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 670905627.2%

반응 단계

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.36 g) and 3,4,5-trifluorobenzonitrile (1.00 g) were heated under argon in xylene (10 ml) containing diisopropylethylamine (3.3 ml) for 16 h. The reaction mixture was cooled and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried and evaporated to give a solid which was triturated with pentane-ether to afford the title product (0.16 g) as an off white powder. Chromatography of the mother liquors on silica gel eluting with ethyl acetate-pentane mixtures afforded further title product (0.92 g). Mass Spectrum (API+): Found 252 (MH+-tBoc). C18H23F2N3O2 requires 351.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741329B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9220fc6e22924dd5bda96f7b809804ba
출처 메모uspto-grants-2010_06