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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241840생성일: 2026년 10월 26일

1,4-Dioxane → 5,6,7,8-Tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/241840

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물DiisopropylethylamineHCID 81531—
반응물2-Chloro-5-methyl-pyridineHCID 581393—
반응물5,6,7,8-Tetrahydropyrido[4,3-d]pyrimidin-4(3H)-oneHCID 135627628—
용매DimethylacetamideHCID 31374—
용매Chloroform isopropyl alcoholHCID 21906603—
생성물5,6,7,8-Tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidin-4(3H)-oneHCID 13597895748.5%

반응 조건

온도150 °C

반응 단계

Into a 20 mL microwave tube was combined 5,6,7,8-tetrahydro-3H-pyrido[4,3-d]pyrimidin-4-one (0.280 g, 1.83 mmol), 2-chloro-5-methylpyridine (0.47 g, 3.7 mmol), 1,4-dioxane (2.5 mL), N,N-diisopropylethylamine (0.64 mL, 3.7 mmol) and N,N-dimethylacetamide (0.5 mL). The mixture was heated via microwave at 150° C. for 4 hours. The mixture was reduced in vacuo and taken up in chloroform:IPA (3:1) (50 mL). The organic phase was washed with sodium bicarbonate and brine (1×50 mL), dried over sodium sulfate, and reduced in vacuo. The residue was purified by flash chromatography on silica gel (0-10% methanol/methylene chloride) to give a bright yellow solid (0.215 g, 47.9%). MS: 243.3 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653091B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-ee487f9731e740129df005f175727be1
출처 메모uspto-grants-2014_02