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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452생성일: 2026년 10월 23일

Pyridine → 6-dimethylaminocarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone

https://huagongshe.com/ko/reaction/1452

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Dimethylamine, hydrochlorideHCID 10473—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690715—
용매TetrahydrofuranHCID 8028—
생성물6-dimethylaminocarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 1969068532%

반응 단계

To a stirred solution of 0.87 g (3.2 mmol) of crude 6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone, 0.32 g (3.9 mmol) of dimethylamine hydrochloride and 2 mL of pyridine in 10 mL of THF was added 0.74 g (3.6 mmol) of solid N,N'-dicyclohexylcarbodiimide. The mixture was stirred at room temperature for 4 days and filtered to remove insoluble material. The filtrate was diluted with 150 mL of ethyl acetate, washed with 50 mL of 5% aqueous HCl and 50 mL of saturated aqueous sodium bicarbonate and dried over MgSO4. Removal of the solvent left 0.40 g of crude product which was purified by flash chromatography on a 30 g column of silica gel, eluted with 60, 80 and 100% ethyl acetate in hexanes to furnish 0.30 g (32%) of 6-dimethylaminocarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone (compound 19), mp 137°-140° C. 1H-NMR (CDCl3) δ 2.15(3H,s), 2.40(1H,t), 3.00(3H,s), 3.10(3H,s), 4.65(2H,d), 7.55(3H,m), 7.70(2H,m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726124
출처 데이터셋uspto-grants-1998_03
ORD IDord-21393e26ab0b4c64a67d4dbe4b4c6328
출처 메모uspto-grants-1998_03