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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 900735생성일: 2026년 10월 25일

Water → Ethyl 3-methyl-1-(2-methylpropyl)-2,4-dioxo-1,2,3,4-tetrahydro-thieno[2,3-d]pyrimidine-5-carboxylate

https://huagongshe.com/reaction/900735

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl bromopyruvateHCID 66144—
반응물6-Mercapto-3-methyl-1-(2-methylpropyl)-2,4(1H,3H)-pyrimidinedioneHCID 5282567—
촉매Titanium TetrachlorideHCID 24193—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Ethyl 3-methyl-1-(2-methylpropyl)-2,4-dioxo-1,2,3,4-tetrahydro-thieno[2,3-d]pyrimidine-5-carboxylateHCID 5282568—

반응 단계

6-Mercapto-3-methyl-1-(2-methylpropyl)-pyrimidine-2,4(1H,3H)-dione (49.5 g) was dissolved in dry DMF (900 ml) and ethyl bromopyruvate (30 ml) was added, and then with stirring anhydrous potassium carbonate (15.954 g) was also added. The mixture was stirred at room temperature for 5 h, and then poured into water (5 L). The aqueous solution was acidified with dil hydrochloric acid, and then extracted thoroughly with ethyl acetate. The organic extract was dried (MgSO4) and evaporated at high vacuum to leave a semisolid mass. A portion of this semisolid mass (24 g) was dissolved in methylene chloride (500 ml) and cooled in an ice-bath under an atmosphere of nitrogen. With efficient stirring titanium tetrachloride (13.5 ml) was slowly added. The reaction mixture was stirred 1 h in the ice-bath and then 3 h at room temperature. The reaction mixture was poured slowly into vigorously stirred ice-water (1.5 L), and then the resulting suspension was extracted into methylene chloride. After drying the organic solvent was concentrated in vacuo, and the residue was chromatographed (SiO2/1:1 ethyl acetate-isohexane) to afford the sub-title compound as a pale yellow solid (15 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361660B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-c14fd4ca5aa54af1b9b253ff9abb60b3
출처 메모uspto-grants-2008_04