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HRID 583417作成日:2026年10月27日

Triethylamine → 4-[N'-Methyl-N'-(3,5-bistrifluoromethyl-benzoyl)-amino]-5-(naphth-2-yl)-pentanoic acid N-propyl-N-phenyl-amide

https://huagongshe.com/reaction/583417

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Potassium CarbonateHCID 11430—
反応物Benzenamine, N-propyl-HCID 12153—
反応物4-[N-Methyl-N-(3,5-bistrifluoromethyl-benzoyl)-amino]-5-(naphth-2-yl)-pentanoic acidHCID 21310529—
溶媒DichloromethaneHCID 6344—
生成物4-[N'-Methyl-N'-(3,5-bistrifluoromethyl-benzoyl)-amino]-5-(naphth-2-yl)-pentanoic acid N-propyl-N-phenyl-amideHCID 86754326—

反応手順

A mixture consisting of 100 mg of 4-[N-methyl-N-(3,5-bistrifluoromethyl-benzoyl)-amino]-5-(naphth-2-yl)-pentanoic acid, 29.9 mg of N-propyl-aniline, 85.3 mg of propanephosphonic acid anhydride, 154 νl of triethylamine and 2 ml of methylene chloride is left to stand at room temperature for 18 hours. 0.5 ml of 1N potassium carbonate solution is then added and the mixture is shaken vigorously. After separation of the phases, the organic phase is separated off and concentrated by evaporation. Chromatography of the residue over silica gel with methylene chloride/methanol 19:1 yields the title compound in the form of a yellow foam. Rf value=0.63 (methylene chloride/methanol 19:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929067
出典データセットuspto-grants-1999_07
ORD IDord-9a099cbfe32d42a4b9f05ae2dcf3400c
出典メモuspto-grants-1999_07