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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1934644Erstellt: 26. Oktober 2026

1-Hydroxybenzotriazole → 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

https://huagongshe.com/reaction/1934644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktBenzo-1,3-dioxole-5-methylamineHCID 75799—
Edukt2-Fluoro-5-nitrobenzoic acidHCID 280997—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamideHCID 2246764186,1%

Reaktionsschritte

A mixture of 2-fluoro-5-nitrobenzoic acid (1.00 g), (1,3-benzodioxol-5-ylmethyl)amine (980 mg), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (1.55 g) and 1-hydroxybenzotriazole (1.09 g) in anhydrous dimethylformamide (10 mL) was stirred for 40 hours at ambient temperature. The mixture was partitioned between water and ethyl acetate. The separated organic layer was washed with an aqueous saturated sodium bicarbonate solution, 1N-hydrochloric acid, water and brine. Then, the resultant was dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide as yellow powders (1.48 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06384080B1
Quelldatensatzuspto-grants-2002_05
ORD IDord-829a96a6ccff41a995f08c54de850f1f
Quellennotizuspto-grants-2002_05