돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2067908생성일: 2026년 10월 26일

Methyl isonipecotate → Methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/2067908

반응식

참여 물질

역할이름HCID투입량
반응물Methyl isonipecotateHCID 424914—
반응물2-(5-(5-Bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl methanesulfonateHCID 86660123—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylateHCID 58542307—

반응 조건

온도90 °C

반응 단계

2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl methanesulfonate 46b (0.24 mmol) and methyl piperidine-4-carboxylate (0.48 mmol) are dissolved in NMP (2 mL) and heated to 90° C. for 3 h. The reaction mixture is cooled to rt and diluted with water and extracted with EtOAc (2×30 mL). The organic layer is washed with water, brine, dried over sodium sulfate, and concentrated to dryness. The crude product is purified by short SiO2 chromatography using DCM:hexane=9:1 as eluant to yield methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylate 47 as light brown solid. MS (m/z) (M+1)+: 454.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08293757B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-5eacd9c8f44141448122ab8b1c12f878
출처 메모uspto-grants-2012_10