돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745620생성일: 2026년 10월 26일

4-Methyl-2-oxovaleric acid → HCID 14303083, 화합물

https://huagongshe.com/reaction/745620

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-2-oxovaleric acidHCID 70—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물O-methyl-L-tyrosine N-MethylamideHCID 14303038—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물HCID 14303083HCID 1430308372.3%

반응 단계

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.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04599361
출처 데이터셋uspto-grants-1986_07
ORD IDord-1f725cf520964bd6aca9cf2131cdfefd
출처 메모uspto-grants-1986_07