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HRID 230275作成日:2026年10月27日

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

https://huagongshe.com/reaction/230275

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetoacetateHCID 8868—
反応物4-CyanobenzaldehydeHCID 66042—
反応物3-(Trifluoromethyl)phenylthioureaHCID 735844—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylateHCID 57762441—

反応手順

3-Trifluoromethylphenyl thiourea (3.00 g, 13.6 mmol), 4-cyanobenzaldehyde (3.57 g, 27.3 mmol) and ethyl acetoacetate (3.55 g, 27.3 mmol) are dissolved in 50 ml THF. Ethyl polyphosphate (4.50 g) is added and the reaction mixture is stirred at reflux temperature overnight. After cooling to room temperature, it is quenched with 50 ml of water and extracted with 100 ml ethyl acetate (2×). The combined organic layers are dried with sodium sulfate and the solvent is removed in vacua. The product is purified via preparative HPLC (RP18-column; eluent: acetonitrile-water, gradient 10:90 to 90:10).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566723B2
出典データセットuspto-grants-2009_07
ORD IDord-75a4783c934b477b8d5d8631cc587d0f
出典メモuspto-grants-2009_07