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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Cyanobenzaldehyde | HCID 66042 | — |
| 반응물 | 3-(Trifluoromethyl)phenylthiourea | HCID 735844 | — |
| 반응물 | 2-Cyanoethyl 3-oxobutanoate | HCID 12360406 | — |
| 반응물 | Trimethyl(phosphooxy)silane | HCID 16133246 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-Cyanoethyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate | HCID 86605135 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07566723B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-87e2a632ae6143e5a1fa27957dd45260 |
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| 출처 메모 | uspto-grants-2009_07 |
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