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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 337637Erstellt: 24. Oktober 2026

Benzoic acid, 3,5-dibromo- → 3,5-dibromo-N-cyclopropylbenzamide

https://huagongshe.com/de/reaction/337637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic acid, 3,5-dibromo-HCID 12063—
EduktCyclopropylamineHCID 69828—
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylformamideHCID 6228—
Produkt3,5-dibromo-N-cyclopropylbenzamideHCID 67062088—

Reaktionsschritte

To a stirred solution of 3,5-dibromobenzoic acid (1 eq.) in DMF (0.15 M) was added HATU (1.3 eq.), cyclopropylamine (1.1 eq.) and Hunig's base (3 eq.). The resulting yellow mixture was stirred at RT for 18 h. The reaction was then quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic extracts were washed further with water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Trituration of the crude product thus obtained in a mixture of ether and hexanes afforded the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889714B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-3e4244c5b4c2486dbba4e4862f388986
Quellennotizuspto-grants-2014_11