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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

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(3-Methyl-1,2-oxazol-5-yl)methanamine hydrochlorideHCID 45792534—
반응물5-bromo-2-chloro-N-(5-methyl-1H-pyrazol-3-yl)-4-PyrimidinamineHCID 50993645—
용매1-ButanolHCID 263—
생성물5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidineHCID 6015428531%

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521453B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-cf5dbee485fe4d8dbb0df7bc2ba3b85d
출처 메모uspto-grants-2009_04