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HRID 345030作成日:2026年10月26日

N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamine → N-methyl-N-(5-aminobenzoxazol-2-ylmethyl)-4-aminophenethylamine

https://huagongshe.com/reaction/345030

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethylamineHCID 19813428—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
生成物N-methyl-N-(5-aminobenzoxazol-2-ylmethyl)-4-aminophenethylamineHCID 19813431—

反応手順

N-Methyl-N-(5-nitrobenzoxazol-2-ylmethyl)-4-nitrophenethyl-amine (0.78 g, 2.2 mmole) in ethanol (50 ml) containing Raney nickel (0.1 g) was stirred under a hydrogen atmosphere (50 psi =344.7 kPa) for 18 hours, by which time thin layer chromatographic analysis showed that all the starting material had been consumed [silica chromatography plates using methylene chloride/methanol (19:1) as the solvent]. The reaction mixture was then filtered and evaporated to give an oil which was azeotroped with toluene and triturated with ether. The decanted ether was evaporated to give the title compound as an oil, which was used directly without further purification, yield 0.45 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05055473
出典データセットuspto-grants-1991_10
ORD IDord-bef763eb70a0459698faf26f3e4eec1a
出典メモuspto-grants-1991_10