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HRID 926884作成日:2026年10月25日

2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide → 2-amino-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide

https://huagongshe.com/reaction/926884

反応式

関与物質

役割名称HCID仕込み量
反応物2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamideHCID 68069774—
触媒PalladiumHCID 23938—
溶媒Dichloromethane methanolHCID 21226129—
生成物2-amino-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamideHCID 6658741194.4%

反応手順

Into a 100-mL round-bottom flask, was placed a solution of 2-nitro-5-(piperidin-1-yl)-N-(1-(3-(trifluoromethyl)phenyl)-1H-imidazol-4-yl)benzamide (600 mg, 1.11 mmol, 1.00 equiv, 85%) in methanol/dichloromethane (10/5 mL). The mixture was treated with Pd/C (600 mg) and stirred under an atmosphere of hydrogen overnight at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum to give 450 mg (85%) of product as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09289430B2
出典データセットuspto-grants-2016_03
ORD IDord-042e25c968224bbfa85304435eb5a051
出典メモuspto-grants-2016_03