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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72669생성일: 2026년 10월 24일

2-Thiophenecarboxylic acid → 6-[4-(Methylsulfonyl)phenyl]-5-phenyl-4-[4-(2-thienyl carbonyl)piperazin-1-yl]-2-(trifluoromethyl)pyrimidine

https://huagongshe.com/ko/reaction/72669

반응식

참여 물질

역할이름HCID투입량
반응물2-Thiophenecarboxylic acidHCID 10700—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물6-[4-(Methylsulfonyl)phenyl]-5-phenyl-4-piperazin-1-yl-2-(trifluoromethyl)pyrimidineHCID 58089453—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물6-[4-(Methylsulfonyl)phenyl]-5-phenyl-4-[4-(2-thienyl carbonyl)piperazin-1-yl]-2-(trifluoromethyl)pyrimidineHCID 5808938848.6%

반응 조건

온도37 °C

반응 단계

To a solution of 6-[4-(methylsulfonyl)phenyl]-5-phenyl-4-piperazin-1-yl-2-(trifluoromethyl)pyrimidine (0.2 g, 0.43 mmol, prepared according to the procedure described in preparation 2) in DMF (20 ml) was added thiophene-2-carboxylic acid (0.149 g, 0.78 mmol) under stirring at 37° C. and then after 10 minutes EDCI (0.149 g, 0.78 mmol), and HOBt (0.023 g, 0.173 mmol) were added. Further TEA (0.179 ml, 2.9 mmol) was added to the resultant clear solution and it was stirred for 18 hours. Subsequently the reaction mixture was diluted with ethyl acetate (50 ml) and the organic layer was washed successively with water, 10% sodium bi carbonate solution (100 ml) and brine (100 ml) respectively and dried over anhydrous sodium sulphate. Evaporation of the solvent and purification by column chromatography (0.4% MeOH: DCM) gave the title compound (0.12 g, yield 48.6%); m.p. 189-194° C. 1H-NMR (CDCl3) δ: 2.98 (s, 3H), 3.4-3.41 (t, 4H), 3.66-3.68 (t, 4H), 7.02-7.77 (m, 12H); MS m/z: 573.2 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828999B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-875ce347f0ab407ea6111ea0d294befd
출처 메모uspto-grants-2014_09