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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1934645Erstellt: 25. Oktober 2026

2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide → HCID 178522768, Verbindung

https://huagongshe.com/reaction/1934645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamideHCID 22467641—
EduktHCID 178511715HCID 178511715—
LösungsmittelPyridineHCID 1049—
ProduktHCID 178522768HCID 17852276884,2%

Reaktionsschritte

To a solution of 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide (150 mg) in anhydrous pyridine (3 mL) was added trans-4-aminocyclohexanol (81.4 mg), and the mixture was stirred for 15 hours at ambient temperature, and then for 3 hours at 60° C. The mixture was partitioned between ethyl acetate and water. The separated organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was subjected to a silica gel column chromatography eluting with a mixture of chloroform and methanol (20:1). The eluent was concentrated and the residue was triturated with diisopropyl ether to give 2-(trans-4-hydroxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide as yellow powders (164 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06384080B1
Quelldatensatzuspto-grants-2002_05
ORD IDord-51cea3d5a0df4652af0750f4f91785be
Quellennotizuspto-grants-2002_05