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HRID 247120作成日:2026年10月26日

N-Methylbenzylamine → 3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/247120

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylbenzylamineHCID 7669—
反応物TriethylamineHCID 8471—
反応物3-(3-Amino-1,2,4-oxadiazol-5-yl)-1-azabicyclo(2.2.1)heptaneHCID 163938—
溶媒TetrahydrofuranHCID 8028—
生成物3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazoleHCID 2016122151.7%

反応手順

A stirred solution of 8.0 g of the oxadiazole prepared above, 9.26 g of N-methylbenzylamine and 10.32 g of triethylamine in 50 ml of THF was allowed to stand at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate. The resultant solution was washed with water, dried and evaporated in vacuo. The residue was chromatographed on silica gel using benzeneethyl acetate (2:1) as eluent to give 5.56 g of 3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazole as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705786
出典データセットuspto-grants-1987_11
ORD IDord-d472f0b3857543bf941249551c0b37ea
出典メモuspto-grants-1987_11