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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Isopropenyl chloroformate | HCID 93846 | — |
| 반응물 | 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 | HCID 68998560 | — |
| 생성물 | 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 | HCID 68999050 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07419988B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-186d9950e3c94713a2ce7d946f82bcf6 |
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| 출처 메모 | uspto-grants-2008_09 |
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