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HRID 502709作成日:2026年10月25日

1-Methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazine → 2-(4-Methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamine

https://huagongshe.com/reaction/502709

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazineHCID 68463407—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物2-(4-Methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamineHCID 59427881—

反応手順

1-methyl-4-(2-nitro-4-(trifluoromethyl)phenylsulfonyl)piperazine was dissolved in EtOH (20 mL) and the solution was purged with argon. Pd/C (365 mg, 0.34 mmol, 10%) was added to the solution, which was stirred for 3 days in an atmosphere of hydrogen gas. The mixture was again purged with argon, filtered through Celite and concentrated under reduced pressure to afford 2-(4-methylpiperazin-1-ylsulfonyl)-5-(trifluoromethyl)benzenamine. MS m/z=324 [M+H]+. Calc'd for C12H16F3N3O2S: 323.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07776869B2
出典データセットuspto-grants-2010_08
ORD IDord-fe3194fcb5fd4f988c4e7f92d31d19e7
出典メモuspto-grants-2010_08