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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74904생성일: 2026년 10월 26일

Diisopropylethylamine → Tert-butyl 2-[[[2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-pyrimidin-4-yl]amino]methyl]-4,4-difluoro-piperidine-1-carboxylate

https://huagongshe.com/reaction/74904

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Chloro-3-(5-fluoro-4-methylsulfinyl-pyrimidin-2-yl)-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridineHCID 67285321—
반응물Tert-butyl 2-(aminomethyl)-4,4-difluoropiperidine-1-carboxylateHCID 67286116—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 2-[[[2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-pyrimidin-4-yl]amino]methyl]-4,4-difluoro-piperidine-1-carboxylateHCID 67285095—

반응 조건

온도130 °C

반응 단계

To a solution of tert-butyl 2-(aminomethyl)-4,4-difluoro-piperidine-1-carboxylate, 13i, (0.10 g, 0.41 mmol) and 5-chloro-3-(5-fluoro-4-methylsulfinyl-pyrimidin-2-yl)-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine (0.18 g, 0.38 mmol) in THF (2 mL) was added iPr2NEt (0.20 mL, 1.15 mmol). The reaction mixture was heated in microwave at 130° C. for 15 minutes. The reaction was cooled to room temperature and the volatiles were removed under reduced pressure. The crude residue was purified via silica gel chromatography (0-100% EtOAc/hexanes) to afford the desired product, 13j.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829007B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8df09fbaa8834d63a654d4669d088ce9
출처 메모uspto-grants-2014_09