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HRID 601988作成日:2026年10月26日

Tetrahydrofuran → N-cyclopentylmethyl-3,5-dimethoxy-(2-propynyloxy)benzamide

https://huagongshe.com/reaction/601988

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物CyclopentanemethylamineHCID 80153—
反応物3,5-Dimethoxy-4-(2-propynyloxy)benzoyl chlorideHCID 57445669—
溶媒Ethyl AcetateHCID 8857—
生成物N-cyclopentylmethyl-3,5-dimethoxy-(2-propynyloxy)benzamideHCID 86630486—

反応手順

To a mixture of 5 ml of THF and 0.30 g of 3,5-dimethoxy-4-(2-propynyloxy)benzoyl chloride were added 0.15 g of 1-(cyclopentyl)methylamine and 0.21 g of triethylamine in order at room temperature. The mixture obtained was stirred at room temperature for 1 hour. Then, ethyl acetate was added to the reaction mixture and the mixture was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.13 g of N-cyclopentylmethyl-3,5-dimethoxy-(2-propynyloxy)benzamide (hereinafter, described as the compound 30 of the present invention) represented by the formula:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902400B2
出典データセットuspto-grants-2011_03
ORD IDord-015122d8d0994657b0da4eacfc1f8910
出典メモuspto-grants-2011_03