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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1897007생성일: 2026년 10월 26일

2,4-Pentanedione, 3-benzyl- → 4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine

https://huagongshe.com/reaction/1897007

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Pentanedione, 3-benzyl-HCID 97757—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amineHCID 608952—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamineHCID 22174870—

반응 조건

온도75 °C

반응 단계

A suspension of 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (5.25 g, 25.6 mmol), 3-benzylpentane-2,4-dione (5.0 g, 28.4 mmol), and p-toluenesulfonic acid monohydrate (0.475 g, 2.50 mmol) in dimethylsulfoxide (50 mL) was heated to 75° C. for 20 hours. The reaction mixture was allowed to cool to room temperature, and the suspension was dissolved in methylene chloride (700 mL). The solution was washed three times with water, once with brine, dried (magnesium sulfate), and concentrated to afford a moist solid. The crude product was suspended in ethyl acetate (50 mL), heated to reflux, allowed to cool to room temperature, and filtered (repeated three times). The final product was obtained as a white solid containing 3% dimethylsulfoxide by weight: 8.63 g (90%). 1H NMR (CDCl3) δ 8.84-8.53 (m, 1H), 8.48 (d, J=7.9 Hz, 1H), 7.86-7.91 (m, 1H), 7.46-7.50 (m, 1H), 7.13-7.30 (m, 5H), 6.61 (br s, 1H), 6.40 (br s, 1H), 3.83 (s, 2H), 2.79 (s, 3H), 2.24 (s, 3H) ppm. MS (ESI) m/z 358 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518999B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-1b737053ca0a48c0bcb7b8c98ae7615d
출처 메모uspto-grants-2013_08