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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45085생성일: 2026년 10월 25일

Methanol → tert-Butyl 6-methyl-4-oxo-4,5,6,8-tetrahydropyrido[3,4-d]pyrimidine-7(1H)-carboxylate

https://huagongshe.com/reaction/45085

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium formateHCID 2723923—
반응물6-methyl-7-(1-phenyl-ethyl)-5,6,7,8-tetrahydro-3H-pyrido[3,4-d]pyrimidin-4-oneHCID 136158781—
촉매PalladiumHCID 23938—
생성물tert-Butyl 6-methyl-4-oxo-4,5,6,8-tetrahydropyrido[3,4-d]pyrimidine-7(1H)-carboxylateHCID 136158782—

반응 단계

To a mixture of 6-methyl-7-(1-phenyl-ethyl)-5,6,7,8-tetrahydro-3H-pyrido[3,4-d]pyrimidin-4-one, (6.8 g, 25.2 mmol), ammonium formate (7.96 g, 126 mmol), BOC-anhydride (8.27 g, 37.9 mmol), MeOH (250 mL), and THF (167 mL) is added 10% Pd/C (1.36 g, 20% w/w) and the reaction is heated at reflux for 3 h. The mixture is then filtered through a Celite® pad and the filterate is concentrated. The residue is purified via FCC (1-10% MeOH/DCM) to give the title compound. MS (ESI) m/z 266.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541432B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-655762ba74914a85a71bf69420625df8
출처 메모uspto-grants-2013_09