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HRID 13529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/13529

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 a suspension of 1 (270 mg, 0.9 mmol) and Lindlar catalyst (192 mg, 10 mol %) in methanol (5 mL), and was then placed on a Parr shaker. The was reaction pressurized with H2 (60 psi) and maintained for 1 h. The reaction was filtered through Celite and the remained solids were washed with methanol. The combined organics were concentrated to give 2 as a brown semi-solid which was carried forward without further purification LCMS m/z 273.3 (MH+), tR=1.56 min.

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-39232e59ed3b4d1687c551e770f893c2
出典メモuspto-grants-2010_06