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HRID 230274作成日:2026年10月26日

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

https://huagongshe.com/reaction/230274

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物4-CyanobenzaldehydeHCID 66042—
反応物3-(Trifluoromethyl)phenylthioureaHCID 735844—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(4-cyanophenyl)-6-methyl-2-thioxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydro-5-pyrimidinecarboxylateHCID 57762471—

反応手順

3-Trifluoromethylphenyl thiourea (200 mg, 0.91 mmol), 4-cyanobenzaldehyde (238.2 mg, 1.82 mmol) and methyl acetoacetate (211 mg, 1.82 mmol) are dissolved in 5 ml THF. Ethyl polyphosphate (0.30 g) is added and the reaction mixture is stirred at reflux temperature overnight. After cooling to room temperature, the reaction is quenched with 10 ml of water and extracted with 10 ml ethyl acetate (2×). The combined organic layers are dried with sodium sulfate and the solvent is removed in vacuo. 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-423d44f2d1b94d9b8d882b391c16cd6f
出典メモuspto-grants-2009_07