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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2093684생성일: 2026년 10월 26일

Trimethyl Phosphate → (R)-8-cyclopentyl-7-ethyl-5-methyl-2-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/reaction/2093684

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl PhosphateHCID 10541—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물HCID 178455829HCID 178455829—
용매1,4-DioxaneHCID 31275—
생성물(R)-8-cyclopentyl-7-ethyl-5-methyl-2-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)-7,8-dihydropteridin-6(5H)-oneHCID 5840587950%

반응 단계

To a solution of (R)-8-cyclopentyl-7-ethyl-2-(2-hydroxypyridin-4-yl)-5-methyl-7,8-dihydropteridin-6(5H)-one (Example 14, 200 mg, 0.6 mmol) in 5 mL of 1,4-dioxane, DBU (26 mg, 3 mmol) and PO(OMe)3 (42 mg, 3 mmol) were added, and the mixture was heated to reflux for 18 h, then concentrated under reduced pressure, and extracted with EtOAc. The combined organic phase was dried with Na2SO4, concentrated under reduced pressure and the residue was chromatographed (PE:EA=1:1) to give the title compound as a yellow solid (100 mg, 50% yield). 1H NMR (CDCl3) δ: 7.95 (s, 1H), 7.53 (s, 1H) 7.35 (d, 1H), 7.11 (m, 1H), 4.54 (m, 1H), 4.29 (m, 1H), 3.6 (s, 3H), 3.38 (s, 3H), 2.2-1.6 (m, 10H) and 0.87 ppm (t, 3H); LCMS: 368.2 m/z (M+H)+; ret. Time: 1.53 min (Analytical Method E).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08445503B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-7102098fa7b84957817401185cfad9db
출처 메모uspto-grants-2013_05