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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2234492Erstellt: 25. Oktober 2026

4-Amino-3-fluorobenzoic acid → 4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamide

https://huagongshe.com/reaction/2234492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Amino-3-fluorobenzoic acidHCID 9971—
EduktDiisopropylethylamineHCID 81531—
Edukt1-Ethylpiperidin-4-amineHCID 3734990—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamideHCID 5510278222,7%

Reaktionsschritte

4-amino-3-fluorobenzoic acid (2.115 g, 13.6 mmol), 4-Amino-1-Ethyl Piperidine (Fluorochem; 1.923 g, 15 mmol), HATU (5.7 g, 15 mmol) and DIPEA (7.1 mL, 40.8 mmol) were combined in DMA (60 mL) and the resulting yellow solution stirred at room temperature for 20 minutes. The reaction was left over the weekend at room temperature, solvent evaporated and the residue dissolved in methanol (10 mL) and loaded onto an SCX-2 column (50 g) which pre-wet with MeOH (40 mL), flushed with MeOH (4×30 ml) and eluted with 7N ammonia in MeOH (4×30 mL). Product containing, ammoniacal fractions were combined to yield the title compound as a brown solid (0.819 g, 22%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07709471B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-60cb88dc051744b899d25578ed6a4372
Quellennotizuspto-grants-2010_05