돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230281생성일: 2026년 10월 25일

4-Cyanobenzaldehyde → 2-Cyanoethyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate

https://huagongshe.com/reaction/230281

반응식

참여 물질

역할이름HCID투입량
반응물4-CyanobenzaldehydeHCID 66042—
반응물3-(Trifluoromethyl)phenylthioureaHCID 735844—
반응물2-Cyanoethyl 3-oxobutanoateHCID 12360406—
반응물Trimethyl(phosphooxy)silaneHCID 16133246—
용매1,4-DioxaneHCID 31275—
생성물2-Cyanoethyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylateHCID 86605135—

반응 조건

온도80 °C

반응 단계

Under argon, trimethylsilyl polyphosphate (10.6 g) is dissolved in 75.7 ml absolute dioxane. To this solution are added 4-cyanobenzaldehyde (5.95 g, 45.4 mmol), 3-trifluoromethylphenyl thiourea (5 g, 22.7 mmol) and 2-cyanoethyl acetoacetate (6.4 g, 45.4 mmol). The reaction mixture is stirred at 80° C. for 3 hours. After evaporation of the dioxane solvent, the residue is dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate solution, 38% sodium bisulfite solution and saturated sodium chloride solution. After drying with magnesium sulfate and evaporating off the solvent, the residue is dissolved in 15 ml methanol and purified by preparative HPLC (column: Kromasil 100 C 185 μm, 30 mm×150 mm; precolumn: Gromsil ODS 4 HE 15 μm, 10 mm×20 mm; flow rate: 66 ml/min; solvent A: acetonitrile, solvent B: water; gradient: 0 min 10% A, 3 min 10% A, 11 min 90% A, 13 min 90% A, 13.2 min 10% A, 15 min 10% A; wavelength: 220 nm; injection volume: approx. 2000 μl; number of injections: 12). The product containing fractions are combined and concentrated in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566723B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-87e2a632ae6143e5a1fa27957dd45260
출처 메모uspto-grants-2009_07