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HRID 745620作成日:2026年10月27日

4-Methyl-2-oxovaleric acid → N-(4-Methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-Methylamide

https://huagongshe.com/reaction/745620

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-2-oxovaleric acidHCID 70—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物O-methyl-L-tyrosine N-MethylamideHCID 14303038—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-(4-Methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-MethylamideHCID 1430308372.3%

反応手順

4-Methyl-2-oxopentanoic acid (31.3 g., 0.24 mol.) was dissolved in dry dichloromethane (50 mls.) and the resultant solution was cooled to 0° C. To the solution was added dropwise oxalyl chloride (23.2 mls., 0.265 mol.), followed by dimethylformamide (0.5 ml.). The resultant mixture was stirred at 0° C. for 1 hour, and then heated under reflux for 5 minutes and then allowed to cool. O-Methyl-L-tyrosine N-Methylamide (50.0 g., 0.24 mol.) and triethylamine (37.1 mls., 0.265 mol.) were dissolved in dichloromethane (120 mls.) and the resultant solution added dropwise to the cooled reaction mixture. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was poured into water (50 mls.) and the organic layer was removed. The aqueous layer was extracted with dichloromethane (30 mls.), the combined extracts were dried over anhydrous sodium sulfate and the solvent removed by evaporation in vacuo to yield a crude product as a yellow solid (85.1 g.). The crude product was recrystallized from tertiary butyl ethyl ether to yield N-(4-methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-methylamide (55.6 g.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04599361
出典データセットuspto-grants-1986_07
ORD IDord-1f725cf520964bd6aca9cf2131cdfefd
出典メモuspto-grants-1986_07