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HRID 13527作成日:2026年10月26日

2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamine → 3-Fluoro-4-(4-methylpiperazin-1-yl)benzene-1,2-diamine

https://huagongshe.com/reaction/13527

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamineHCID 22040816—
触媒Lindlars catalystHCID 131709914—
溶媒MethanolHCID 887—
生成物3-Fluoro-4-(4-methylpiperazin-1-yl)benzene-1,2-diamineHCID 22040743—

反応手順

A reaction tube was charged with suspension of 1 (330 mg, 1.15 mmol) and Lindlar catalyst (245 mg, 10 mol %) in methanol (5 mL), sealed, and placed on a Parr shaker. The reaction was pressurized with H2 (60 psi) and maintained for 1 h. The reaction was filtered through Celite and the remaining solids were washed with MeOH. The combined organics were concentrated to give 2 as a brown semi-solid which was taken on without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-b56fa7ba221548dbbcd91662f6c207a0
出典メモuspto-grants-2010_06