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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28894생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/28894

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isopropenyl chloroformateHCID 93846—
반응물Thiomorpholine 1,1-dioxideHCID 6484228—
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]-4-thiomorpholinecarboxamide 1,1-dioxideHCID 5898000330%

반응 단계

To a solution of 4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)aniline (0.25 mmol) in anhydrous THF (2 mL) cooled to 5° C., was added triethylamine (4 mmol) and isopropenyl chloroformate (0.5 mmol). The reaction mixture was stirred overnight at room temperature. Thiomorpholine 1,1-dioxide (2.5 mmol) was added and the reaction heated at 50° C. for three days. The crude reaction was purified by reverse phase chromatography to give the title product (30%). ESMS [M+H]+: 640.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419988B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-abf75457714741d6972343e0af14de02
출처 메모uspto-grants-2008_09