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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1284411생성일: 2026년 10월 23일

1,3-Dioxolane, 2-(bromomethyl)- → 4-(1,3-Dioxolan-2-ylmethoxy)-6-methoxy-2-pyrimidinamine

https://huagongshe.com/ko/reaction/1284411

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-Amino-6-methylpyrimidin-4-oneHCID 135402055—
용매DimethylformamideHCID 6228—
생성물4-(1,3-Dioxolan-2-ylmethoxy)-6-methoxy-2-pyrimidinamineHCID 2025150016.9%

반응 단계

A solution of 8.5 g (0.060 mol) 2-amino-6-methyl-4-pyrimidinone in 45 mL anhydrous dimethylformamide (DMF) was treated with 6.7 g (0.060 mol) potassium t-butoxide then stirred for 10 minutes at ambient temperature. Subsequently, 7.6 mL (0.073 mol) of 2-bromomethyl-1,3-dioxolane was added and the mixture heated to 120° for 3 hours. The DMF was then evaporated under reduced pressure and the residue partitioned between water and ethyl acetate. The aqueous phase was extracted with two additional portions of ethyl acetate then the combined organic phase was washed with water, brine, then dried (MgSO4) and evaporated to an oil. Chromatography on silica gel with 10% ethyl acetate/CH2Cl2 as the eluant afforded 2.3 g of the title compound as a viscous oil. NMR (CDCl3): δ 3.9 (s, 3H), 4.0 (m, 4H), 4.3 (d, J=4 Hz, 2H), 5.15 (NH, br), 5.27 (t, J=4 Hz, 1H), 5.55 (s, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04563211
출처 데이터셋uspto-grants-1986_01
ORD IDord-1e0c63b1eb114db292b9c1ff6a270ba1
출처 메모uspto-grants-1986_01