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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18082생성일: 2026년 10월 24일

Diisopropylethylamine → 2-(Quinazolin-4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl ester

https://huagongshe.com/ko/reaction/18082

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
반응물4-ChloroquinoxalineHCID 86626011—
용매TetrahydrofuranHCID 8028—
생성물2-(Quinazolin-4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl esterHCID 86626604—

반응 단계

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g), 4-chloroquinoxaline (0.768 g) and diisopropylethylamine (0.816 ml) were dissolved in tetrahydrofuran (75 ml) and heated to reflux for 6 hours under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with saturated sodium hydrogen carbonate solution, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 50 to 100% ethyl acetate in hexane. The title compound was obtained as a white foam (1.44 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741329B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-43773e5d2c34440ca5b5489610e464ec
출처 메모uspto-grants-2010_06