Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2111665생성일: 2026년 10월 26일
Diisopropylethylamine → 5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine
https://huagongshe.com/reaction/2111665
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (3-Methyl-1,2-oxazol-5-yl)methanamine hydrochloride | HCID 45792534 | — |
| 반응물 | 5-bromo-2-chloro-N-(5-methyl-1H-pyrazol-3-yl)-4-Pyrimidinamine | HCID 50993645 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine | HCID 60154285 | 31% |
반응 단계
A mixture of 5-aminomethyl-3-methylisoxazole hydrochloride (890 mg, 6.0 mmol), 5-bromo-2-chloro-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine (Method 1; 578 mg, 2.0 mmol) and N,N-diisopropylethylamine (1.4 ml, 8.0 mmol) in 1-butanol (10 ml) was heated at 120° C. for 18 hours. The mixture was allowed to cool to ambient temperature and volatiles removed by evaporation. The residue was triturated with ether and the product collected by filtration to give the titled compound (225 mg, 31%). 1H NMR (DMSO): δ 2.15 (s, 3H), 2.2 (s, 3H), 4.5 (m, 2H), 6.1 (br s, 2H), 7.6 (br s, 1H), 8.0 (br s, 2H), 12.05 (br s, 1H); MS: m/z 366.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07521453B2 |
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| 출처 데이터셋 | uspto-grants-2009_04 |
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| ORD ID | ord-cf5dbee485fe4d8dbb0df7bc2ba3b85d |
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| 출처 메모 | uspto-grants-2009_04 |
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