돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131554생성일: 2026년 10월 25일

6-Mercapto-3-methyl-1-(2-methylpropyl)-2,4(1H,3H)-pyrimidinedione → Methyl 1-isobutyl-3,6-dimethyl-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-5-carboxylate

https://huagongshe.com/reaction/131554

반응식

참여 물질

역할이름HCID투입량
반응물6-Mercapto-3-methyl-1-(2-methylpropyl)-2,4(1H,3H)-pyrimidinedioneHCID 5282567—
반응물Methyl 3-bromo-2-oxobutanoateHCID 11183175—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Sodium AcetateHCID 517045—
생성물Methyl 1-isobutyl-3,6-dimethyl-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-5-carboxylateHCID 528253259.2%

반응 단계

6-Mercapto-3-methyl-1-(isobutyl)-pyrimidine-2,4(1H,3H)-dione (50 g) was dissolved in a solution of sodium acetate (95.6 g) in water (1.5 L), and methyl 3-bromo-2-oxo-butanoate (44.6 g) was added dropwise with stirring. After stirring 1 h at room temperature the mixture was extracted into ethyl acetate. The organic solution was washed with brine, dried (MgSO4) and evaporated to leave an oil. The oil (75.1 g) was dissolved in methylene chloride (800 ml) and cooled in an ice-bath under an atmosphere of nitrogen. With efficient stirring titanium tetrachloride (43.3 ml) was slowly added dropwise. 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 (2 L), and then the resulting suspension was extracted into methylene chloride. After drying, the organic solvent was removed in vacuo, and the residue was chromatographed (SiO2/1:1 ethyl acetate-isohexane) to afford the sub-title compound 42 g. Trituration with isohexane gave a white powder. δ 1HCDCl3—0.98(6H,d), 2.23-2.41 (1H,m), 2.46 (3H,s), 3.4 (3H,s), 3.75 (2H,d), 3.96 (3H,s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384950B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-3a1efdf513794b83a6209311974c4226
출처 메모uspto-grants-2008_06