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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1862218생성일: 2026년 10월 26일

Bromopinacolone → 5-Ethoxycarbonyl-2-methyl-3-(2-oxo-3,3-dimethyl-butyl)pyrimid-4-one

https://huagongshe.com/reaction/1862218

반응식

참여 물질

역할이름HCID투입량
반응물BromopinacoloneHCID 21642—
반응물Ethyl 4-hydroxy-2-methylpyrimidine-5-carboxylateHCID 293750—
반응물Tetrabutylammonium FluorideHCID 2724141—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-Ethoxycarbonyl-2-methyl-3-(2-oxo-3,3-dimethyl-butyl)pyrimid-4-oneHCID 18619693—

반응 단계

To a suspension of 5-ethoxycarbonyl-2-methylpyrimid-4-one (2.7 g, 14.75 mmol.) in DME (20 ml), tetrabutylammonium fluoride (22 ml, 22.0 mmol.) was added. The solution was stirred at room temperature until solids dissolved, then 1-bromopinacolone (2.2 ml, 1.1 eq., 16.22 mmol) was added. The solution was stirred overnight and concentrated to a brown oil. The crude mixture was purified by silica gel column chromatography (hexane/ethyl acetate, 100/0 to 0/100). A less polar O-alkylated by-product was eluted first (1.8 g) and then the desired N-alkylated product (1.1 g); MS (281, M+H)+. NMR (CDCl3, δ): 8.57 (1H, s) , 5.06(1H, s), 4.35(2H, q), 2.42 (3H, s), 1.34 (3H, t), 1.30 (9H,s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06537998B1
출처 데이터셋uspto-grants-2003_03
ORD IDord-48787509fcbd49089b41334e8d0e00ac
출처 메모uspto-grants-2003_03