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HRID 2170750作成日:2026年10月26日

2-Phenyl-1H-imidazole-4-carbaldehyde → (1-((2-Phenyl-1H-imidazol-5-yl)methyl)piperidin-4-yl)(3-(trifluoromethyl)phenyl)-methanone

https://huagongshe.com/reaction/2170750

反応式

関与物質

役割名称HCID仕込み量
反応物2-Phenyl-1H-imidazole-4-carbaldehydeHCID 3539090—
反応物4-(3-Trifluoromethylbenzoyl)piperidineHCID 5086447—
溶媒DichloromethaneHCID 6344—
生成物(1-((2-Phenyl-1H-imidazol-5-yl)methyl)piperidin-4-yl)(3-(trifluoromethyl)phenyl)-methanoneHCID 7173742354%

反応手順

To piperidin-4-yl(3-(trifluoromethyl)phenyl)methanone (1-1) (147 mg, 0.50 mmol) and 2-phenyl-1H-imidazole-5-carbaldehyde (1-2) (86 mg, 0.50 mmol) in 10 mL of CH2Cl2 was added MP-BH(OAc)3 (200 mg, 0.4 mmol), and the mixture was stirred at room temperature for 16 h. The reaction was filtered to remove the resin, and the filtrate was concentrated under a stream of N2 gas. The crude product was purified by reversed phase HPLC to give 111 mg (54%) of 1-3. HRMS (ES) 414.1786 (M+H) found, 414.1788 required.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09051299B2
出典データセットuspto-grants-2015_06
ORD IDord-4842090627664c0f8e69debf2e0aa58e
出典メモuspto-grants-2015_06