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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29009생성일: 2026년 10월 23일

Pyridine → 1,1-dimethylethyl 4-(5-{4-[3-(4-{[(dimethylamino)carbonyl]amino}phenyl)-1-methyl-1H-pyrazol-4-yl]-1H-pyrrolo[2,3-b]pyridin-2-yl}-2-pyrimidinyl)-1-piperazinecarboxylate

https://huagongshe.com/ko/reaction/29009

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참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Isopropenyl chloroformateHCID 93846—
반응물1,1-dimethylethyl 4-(5-{4-[3-(4-aminophenyl)-1-methyl-1H-pyrazol-4-yl]-1H-pyrrolo[2,3-b]pyridin-2-yl}-2-pyrimidinyl)-1-piperazinecarboxylateHCID 68998560—
생성물1,1-dimethylethyl 4-(5-{4-[3-(4-{[(dimethylamino)carbonyl]amino}phenyl)-1-methyl-1H-pyrazol-4-yl]-1H-pyrrolo[2,3-b]pyridin-2-yl}-2-pyrimidinyl)-1-piperazinecarboxylateHCID 6899905027%

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온도0 °C

반응 단계

To a solution of 1,1-dimethylethyl 4-(5-{4-[3-(4-aminophenyl)-1-methyl-1H-pyrazol-4-yl]-1H-pyrrolo[2,3-b]pyridin-2-yl}-2-pyrimidinyl)-1-piperazinecarboxylate (0.326 mmol) in pyridine (8 ml) under argon at 0° C. was added isopropenyl chloroformate (1.31 mmol) portionwise over 3 hours maintaining the reaction temperature at 0° C. The resulting solution was concentrated, purified by reverse-phase. This intermediate was dissolved in THF (10 ml) and dimethylamine (2M in THF, 20 ml) was added. After heating for 2 hours at 50° C., concentration in vacuo provided the title product (27%) as a yellow solid which was used without further purification. ESMS [M+H]+: 623.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419988B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-186d9950e3c94713a2ce7d946f82bcf6
출처 메모uspto-grants-2008_09