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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1626761Erstellt: 27. Oktober 2026

Sodium Iodide → 5-Chloro-2-({[4-(diphenylmethyl)piperazine-1-yl]acetyl}amino)benzoic acid

https://huagongshe.com/reaction/1626761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktBenzhydrylpiperazineHCID 70048—
EduktDiisopropylethylamineHCID 81531—
Edukt5-Chloro-2-((2-chloroacetyl)amino)benzoic acidHCID 4179825—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-Chloro-2-({[4-(diphenylmethyl)piperazine-1-yl]acetyl}amino)benzoic acidHCID 6668013411%

Reaktionsschritte

1.0 g (4.0 mmol) of 5-chloro-2-[(chloroacetyl)amino]benzoic acid obtained in Example 72-(i), 1.0 g (4.0 mmol) of 1-benzhydrylpiperazine, 1.1 g (8.8 mmol) of N,N-diisopropylethylamine, and 60 mg (0.4 mmol) of sodium iodide were stirred in 5 mL of DMF solution at 80° C. for 3 hours. Thereafter, the solvent was distilled off under reduced pressure, H2O was added to the residue, and solids were collected by filtration and dried. The obtained crude product was separated and purified by silica gel column chromatography, and the resultant was then recrystallized using ethyl acetate/n-hexane, thereby giving 198 mg of the target 5-chloro-2-({[4-(diphenylmethyl)piperazine-1-yl]acetyl}amino)benzoic acid (yield: 11%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08785473B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-f5a441c3ef914f4c8480e170a23a89c2
Quellennotizuspto-grants-2014_07