Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450380생성일: 2026년 10월 25일
Diisopropylethylamine → N2-[(1S)-1-(5-Fluoropyrimidin-2-yl)ethyl]-N4-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidine-2,4-diamine
https://huagongshe.com/reaction/450380
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (S)-1-(5-Fluoropyrimidin-2-yl)ethanamine hydrochloride | HCID 66624037 | — |
| 반응물 | HCID 178458615 | HCID 178458615 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N2-[(1S)-1-(5-Fluoropyrimidin-2-yl)ethyl]-N4-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidine-2,4-diamine | HCID 178458663 | 74% |
반응 단계
A mixture of 2-chloro-N-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidin-4-amine (Intermediate 30, 0.2 g) and [(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]amine hydrochloride (Intermediate 15, 0.15 g) in n-BuOH (5 mL) with diisopropylethylamine (1 mL) was stirred at 70° C. for 4 hours. The resulting mixture was diluted with ethyl acetate (20 mL), and washed with brine (10 mL×3). The organic layer was dried and concentrated. The resulting residue was separated by silica gel column (Hexane/Ethyl acetate) to yield 0.2 g of title compound. MS (electrospray): 404 (M+1) for C16H18FN9O3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08486966B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-56b663976e9048a18946e34c79d06c3a |
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| 출처 메모 | uspto-grants-2013_07 |
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