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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241557생성일: 2026년 10월 26일

Formamidine acetate → tert-Butyl 7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

https://huagongshe.com/reaction/241557

반응식

참여 물질

역할이름HCID투입량
반응물Formamidine acetateHCID 160693—
반응물Sodium ethoxideHCID 2723922—
반응물tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—
용매EthanolHCID 702—
생성물tert-Butyl 7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 22707088—

반응 단계

Formamidine acetate (472 mg, 4.52 mmol) in 15.0 mL of absolute ethanol was treated with sodium ethoxide (21 wt % solution in ethanol; 1.7 mL). After 30 min, a solution of the product from Step A above (1.15 g) in 8 mL of absolute ethanol was added, and the mixture was warmed at reflux for 18 h. The dark solution was cooled to room temperature and concentrated under reduced pressure, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate and concentrated to an orange oil. Purification by flash chromatography (silica gel; 2% methanol/dichloromethane as eluant) afforded the title compound as a light yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653059B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-03b7fd8909164bc2bac911665a874d1e
출처 메모uspto-grants-2014_02