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HRID 2113078作成日:2026年10月27日

4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidine → (1H-Benzoimidazol-4-yl)-[6-(4-trifluoromethylphenyl)pyrimidin-4-yl]amine

https://huagongshe.com/reaction/2113078

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidineHCID 16747837—
反応物HCID 178507452HCID 178507452—
生成物(1H-Benzoimidazol-4-yl)-[6-(4-trifluoromethylphenyl)pyrimidin-4-yl]amineHCID 9820006—

反応手順

Analogous to the procedure used to prepare Example 5(b), 4-chloro-6-(4-trifluoromethylphenyl)pyrimidine, Example 5(a), (690 mg, 2.67 mmol) and 4-aminobenzimidazole (296 mg, 2.22 mmol, Astatech) afforded after purification by silica gel chromatography with gradient from 1% to 10% solution of (2 M NH3 in MeOH) in CH2Cl2, the title compound as a yellow solid. MS (ESI, pos. ion.) m/z: 356 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07524874B2
出典データセットuspto-grants-2009_04
ORD IDord-f3efa625d37d4f41bbad27826d4f9664
出典メモuspto-grants-2009_04