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HRID 601993作成日:2026年10月25日

Triethylamine → N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamide

https://huagongshe.com/reaction/601993

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(S)-(+)-1-CyclohexylethylamineHCID 5325951—
反応物3-Fluoro-4-(2-propynyloxy)benzoyl chlorideHCID 57445684—
溶媒Ethyl AcetateHCID 8857—
生成物N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamideHCID 5770121086.4%

反応手順

To a mixture of 5 ml of ethyl acetate and 0.30 g of 3-fluoro-4-(2-propynyloxy)benzoyl chloride were added 0.22 g of (1S)-1-(cyclohexyl)ethylamine and 0.20 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 washed with hexane to obtain 0.37 g of N-((1S)-1-cyclohexylethyl)-3-fluoro-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 37 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-2a5bf7b9c734421d8ef49376c9eceadf
出典メモuspto-grants-2011_03