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HRID 852445作成日:2026年10月25日

N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide → 4'-Trifluoromethyl-biphenyl-2-carboxylic acid [4-(piperazinyl)-phenyl]-amide

https://huagongshe.com/reaction/852445

反応式

関与物質

役割名称HCID仕込み量
反応物N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499401—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物4'-Trifluoromethyl-biphenyl-2-carboxylic acid [4-(piperazinyl)-phenyl]-amideHCID 1120109949.5%

反応手順

A mixture of intermediate (5) (0.19 mole) in methanol (600 ml) and THF (600 ml) was hydrogenated overnight with Pd/C 10% (3 g) as a catalyst. After uptake of hydrogen (1 equivalent), the catalyst was filtered off and the filtrate was evaporated. The residue was triturated in DIPE. The precipitate was filtered off, dried, and dissolved in water. The mixture was alkalinized with Na2CO3 and then extracted with DCM. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 40 g of N-[4-(1-piperazinyl)phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 6).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253157B2
出典データセットuspto-grants-2007_08
ORD IDord-4007bb0b67744df3894341ce59f0a6d3
出典メモuspto-grants-2007_08