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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28893생성일: 2026년 10월 24일

Triethylamine → N-[4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]-1-pyrrolidinecarboxamide

https://huagongshe.com/ko/reaction/28893

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PyrrolidineHCID 31268—
반응물Isopropenyl chloroformateHCID 93846—
반응물4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)anilineHCID 68998168—
용매TetrahydrofuranHCID 8028—
생성물N-[4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]-1-pyrrolidinecarboxamideHCID 5898002237%

반응 조건

온도50 °C

반응 단계

A solution of [4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]amine (0.204 mmol) in tetrahydrofuran (1 mL) was treated with triethylamine (0.8 mmol) and isopropenyl chloroformate (0.3 mmol). The reaction was stirred for 3 h then pyrrolidine (2 mmol) was added and the reaction heated at 50° C. for 18 h. The reaction was concentrated in vacuo and redissolved in methylene chloride (20 mL) and washed with water (2×10 mL). The methylene chloride was evaporated to give the crude produce which was purified using a Gilson reverse phase HPLC to provide the title product (37%). ESMS [M+H]+: 576.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419988B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c52e79243172441e981407178261ad9f
출처 메모uspto-grants-2008_09