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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1808248Erstellt: 25. Oktober 2026

Dimethylformamide → 4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamide

https://huagongshe.com/reaction/1808248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt4-Amino-3-fluorobenzoic acidHCID 9971—
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
EduktHCID 28917627HCID 28917627—
Produkt4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamideHCID 57732241—

Reaktionsschritte

To a mixture of 4-amino-3-fluorobenzoic acid (200.0 mg, 1.289 mmol) and HBTU (490 mg, 1.3 mmol) in DMF (2 mL, 20 mmol) at 0° C. were added N,N-diisopropylethylamine (0.67 mL, 3.9 mmol) and 2-(4-fluorophenoxy)-2-methylpropan-1-amine (Preparation 91, 280 mg, 1.5 mmol). The reaction mixture was slowly warmed to ambient temperature. The reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic layers were washed successively with water, aqueous lithium chloride, and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, chloroform to 12% MeOH in chloroform).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08357711B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-a21d075e470f4516997390ef108200d2
Quellennotizuspto-grants-2013_01