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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887373생성일: 2026년 10월 27일

Potassium Carbonate → N-Benzyl-4-methyl-2-(2-oxo-4-(2-oxoimidazolidin-1-yl)pyridin-1(2H)-yl)thiazole-5-carboxamide

https://huagongshe.com/reaction/1887373

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Chloroethyl isocyanateHCID 16035—
반응물2-(4-Amino-2-oxopyridin-1(2H)-yl)-N-benzyl-4-methylthiazole-5-carboxamideHCID 24985270—
용매DimethylformamideHCID 6228—
생성물N-Benzyl-4-methyl-2-(2-oxo-4-(2-oxoimidazolidin-1-yl)pyridin-1(2H)-yl)thiazole-5-carboxamideHCID 577444726%

반응 조건

온도85 °C

반응 단계

To a solution of 2-(4-amino-2-oxopyridin-1(2H)-yl)-N-benzyl-4-methylthiazole-5-carboxamide (0.14 g, 0.41 mmol) in N,N-dimethylformamide (10 mL) was added 2-chloroethyl isocyanate (0.05 mL, 0.58 mmol) at ambient temperature. The resulting reaction mixture was heated at 80-90° C. for 7 hours. Potassium carbonate (0.10 g, 0.72 mmol) was added and the reaction mixture was heated for 18 hours. The solvent was removed in vacuo, and the residue was purified by column chromatography to afford the title compound in 6% yield (0.01 g): mp>300° C.; 1H NMR (300 MHz, DMSO-d6) δ 8.76 (t, J=6.0 Hz, 1H), 8.56 (d, J=8.4 Hz, 1H), 7.64-7.17 (m, 7H), 6.08 (d, J=2.1 Hz, 1H), 4.38 (d, J=6.0 Hz, 2H), 3.85-3.79 (m, 2H), 3.42-3.37 (m, 2H), 2.60 (s, 3H); 13C NMR (75 MHz, DMSO-d6) δ 161.9, 160.7, 157.8, 153.8, 150.7, 150.4, 139.9, 130.9, 128.7, 127.7, 127.2, 123.7, 101.4, 98.8, 44.3, 43.1, 36.5, 17.5; MS (ES+) m/z 410.2 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501746B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-f3107b58f82644158e381fc4ab4c17a2
출처 메모uspto-grants-2013_08