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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1929537생성일: 2026년 10월 27일

Hydrochloric Acid → 2-(pyridin-3-yl)-4-(2-chloro-4-fluorophenyl)-7,7-dimethyl-4,6,7,8-tetrahydroquinazolin-5(1H)-one

https://huagongshe.com/reaction/1929537

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimedoneHCID 31358—
반응물2-Chloro-4-fluorobenzaldehydeHCID 145024—
반응물Nicotinamidine hydrochlorideHCID 202042—
반응물Sodium AcetateHCID 517045—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(pyridin-3-yl)-4-(2-chloro-4-fluorophenyl)-7,7-dimethyl-4,6,7,8-tetrahydroquinazolin-5(1H)-oneHCID 2503029526%

반응 단계

3-Pyridinecarboxamidine hydrochloride (Schaefer F. C., Peters G. A., et al. J. Org. Chem.; 1961; 26(2); 412-418.) 2.164 mmol, 2-chloro-4-fluorobenzaldehyde 2.164 mmol, 5,5-dimethyl-1,3-cyclohexanedione 2.164 mmol and sodium acetate 3.2 mmol were reacted in 8 ml of anhydrous ethanol under refluxing for 18 hr, condensed, and ethyl acetate and water and 1N HCl were added to separate the layers. The water layer was adjusted with concentrated NaOH solution until the pH to be basic, then ethyl acetate was added and extracted twice. The organic layers were combined, dried over anhydrous sodium sulfate and separated by column chromatography to obtain a yellow solid of 0.22 g (yield 26%); mp 186-187° C. 1H-NMR (400 MHz, CDCl3) δ 1.15 (3H, s, CH3); 1.16 (3H, s, CH3); 2.31 (2H, s, CH2); 2.53-2.69 (2H, m, CH2); 6.07 (1H, s, CH); 6.94-6.96 (1H, m, ArH); 7.14-7.17 (1H, m, ArH); 7.23-7.26 (1H, m, ArH); 7.34-7.38 (1H, m, ArH) 8.07-8.09 (1H, m, ArH); 8.69-8.71 (1H, m, ArH); 8.89 (1H, m, ArH). MS (EI) 383.1 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188091B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-f0135dcc23d648ad9493a2fc9e0c3f90
출처 메모uspto-grants-2012_05