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HRID 634935作成日:2026年10月27日

2,3,5,6-Tetrafluorophenol → tert-Butyl pentanoate

https://huagongshe.com/reaction/634935

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,5,6-TetrafluorophenolHCID 69858—
反応物Potassium FluorideHCID 522689—
反応物N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl esterHCID 86756359—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl pentanoateHCID 520048371.5%
生成物N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl EsterHCID 86756358—

反応手順

Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-carbonyl)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-carbonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetral]uorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06184244B2
出典データセットuspto-grants-2001_02
ORD IDord-6da38b4177ff47fe80c51126986009bb
出典メモuspto-grants-2001_02