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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1409747생성일: 2026년 10월 26일

2-Chloro-5-ethylpyrimidine → (3S,4R)-N-cyclopropyl-1-(5-ethylpyrimidin-2-yl)-3-fluoropiperidin-4-amine

https://huagongshe.com/reaction/1409747

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-ethylpyrimidineHCID 3572763—
반응물tert-butyl N-cyclopropyl-N-[(3S,4R)-3-fluoropiperidin-4-yl]carbamateHCID 68290240—
생성물(3S,4R)-N-cyclopropyl-1-(5-ethylpyrimidin-2-yl)-3-fluoropiperidin-4-amineHCID 68290585—

반응 단계

The title compound is prepared from tert-butyl N-cyclopropyl-N-[(3S,4R)-3-fluoropiperidin-4-yl]carbamate and 2-chloro-5-ethylpyrimidine following a procedure analogous to that described for Intermediate 87. LC (method 20): tR=1.80 min; Mass spectrum (APCI): m/z=265 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921398B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-96d6563191d641cab620d8577d9ce3ac
출처 메모uspto-grants-2014_12