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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2297053생성일: 2026년 10월 26일

2,3,5,6-Tetrafluorophenol → N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester

https://huagongshe.com/reaction/2297053

반응식

참여 물질

역할이름HCID투입량
반응물2,3,5,6-TetrafluorophenolHCID 69858—
반응물Potassium FluorideHCID 522689—
반응물N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl esterHCID 86756359—
용매DimethylformamideHCID 6228—
생성물N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl EsterHCID 86756358—
생성물N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl esterHCID 13172366644%

반응 단계

Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (86.1 mg, 0.149 mmol) and 2,3,5, 6-tetrafluorophenol (27.0 mg, 0.163 mmol in DMF (2.0 ml). After stirring at room temperature for 3 hours, the reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, washed with saturated NaHCO3 solution, and brine, dried over sodium sulfate, and concentrated. The residue was triturated with ether to give the titled product, N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06489353B2
출처 데이터셋uspto-grants-2002_12
ORD IDord-b8a4c2d1154744018ded014a58ca1e72
출처 메모uspto-grants-2002_12