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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58220생성일: 2026년 10월 24일

Adenine → 2-[1-(6-amino-9H-purin-9-yl)ethyl]-3-bromo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/ko/reaction/58220

반응식

참여 물질

역할이름HCID투입량
반응물AdenineHCID 190—
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물3-bromo-2-(1-chloroethyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 66864030—
용매DimethylformamideHCID 6228—
생성물2-[1-(6-amino-9H-purin-9-yl)ethyl]-3-bromo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 6686477210.7%

반응 단계

A mixture of 3-bromo-2-(1-chloroethyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (1.24 g, 4.11 mmol), adenine (Sigma, 1.08 g, 8.04 mmol), and potassium carbonate (1.11 g, 8.04 mmol) in N,N-dimethylformamide (20 mL) was stirred at room temperature overnight. The suspension was then poured into water and extracted with methylene chloride. The combined organic layers were washed with water, brine, and then the organic layers dried and evaporated to dryness. The residue was chromatographed on silica gel, eluting with 0 to 10% MeOH in methylene chloride, to provide the desired product (176 mg, 10.7%). LCMS calculated for C16H15BrN7O (M+H)+: m/z=400.1. Found: 400.1. 1H NMR (DMSO-d6, 300 MHz) δ 8.44 (1H, s), 8.07 (1H, s), 7.67 (1H, dd, J=8.7 and 7.2 Hz), 7.30 (1H, br d, J=8.7 Hz), 7.20 (2H, s), 6.99 (1H, br d, J=7.2 Hz), 6.15 (1H, q, J=7.2 Hz), 2.91 (3H, s), 1.84 (3H, d, J=7.2 Hz) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434746B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-12a77f0195e34611a0daedc0d4367fed
출처 메모uspto-grants-2016_09