Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243823Erstellt: 26. Oktober 2026

Acetohydroxamic Acid → [(Z)-1-aminoethylideneamino] 2-fluoro-6-iodobenzoate

https://huagongshe.com/reaction/243823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetohydroxamic AcidHCID 1990—
EduktDimethylformamideHCID 6228—
EduktOxalyl chlorideHCID 65578—
Edukt2-Fluoro-6-iodobenzoic acidHCID 2733302—
LösungsmittelDichloromethaneHCID 6344—
Produkt[(Z)-1-aminoethylideneamino] 2-fluoro-6-iodobenzoateHCID 87262981—

Reaktionsschritte

Alternately, acid (XXXa) is prepared by first converting 2-fluoro-6-iodobenzoic acid to the acid chloride by reaction with a chlorinating agent such as oxalyl chloride, in a solvent such as DCM, with a catalytic amount of DMF, at a temperature of 0° C. Subsequent reaction of the acid chloride with N-hydroxyacetamide in a solvent such as CH2Cl2 provides (Z)—N′-((2-fluoro-6-iodobenzoyl)oxy)acetimidamide. 5-(2-Fluoro-6-iodophenyl)-3-methyl-1,2,4-oxadiazole is prepared by reacting (Z)—N′-((2-fluoro-6-iodobenzoyl)oxy)acetimidamide with sodium acetate, in a solvent such as tert-butanol, at temperatures ranging from 100° C. to 110° C. 3-Fluoro-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (XXXa) is prepared by reacting 5-(2-fluoro-6-iodophenyl)-3-methyl-1,2,4-oxadiazole with a grignard reagent such as i-PrMgCl, in a suitable solvent such as THF and the like, at a temperature of −78° C. Subsequent addition of CO2 gas, at a temperature of −78° C. provides 3-fluoro-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (XXXa).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653263B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-b85d640b90454778885564ec29979b7f
Quellennotizuspto-grants-2014_02