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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378142Erstellt: 24. Oktober 2026

2-Dimethylaminopyridine → Ethyl beta-[[2-[[(3-nitrophenyl)carbonyl]amino]acetyl]amino]pyridine-3-propanoate

https://huagongshe.com/de/reaction/378142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-DimethylaminopyridineHCID 21885—
EduktGlycine, N-(3-nitrobenzoyl)-HCID 94858—
EduktDi(succinimido) carbonateHCID 676246—
Edukt3-(Ethylamino)propanoic acid hydrochlorideHCID 86759576—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelPotassium CarbonateHCID 11430—
ProduktEthyl beta-[[2-[[(3-nitrophenyl)carbonyl]amino]acetyl]amino]pyridine-3-propanoateHCID 2260859580%

Reaktionsschritte

The same procedure used in the preparation of Example C was followed substituting an equivalent amount of DL-ethyl 3-amino-3-pyridyl propionate for ethyl beta-alanine hydrochloride. N,N'-Disuccinimidyl carbonate (14 g, 5.5 mmol) was added to 3-nitro-benzoyl glycine (10 g, 4.5 mmol) in dry dimethylformamide (30 mL) followed by dimethylaminopyridine (200 mg). After a period of 1 hour DL-ethyl 3-amino-3-(3-pyridyl) propionate dihydrochloride (13 g, 4.6 mmol) in 20% aqueous potassium carbonate (50 mL) was added in one portion. After complete reaction the product was collected by filtration (11.5 g, 80% yield). MS and 1H-NMR were consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06028223
Quelldatensatzuspto-grants-2000_02
ORD IDord-b5d2c8a532754646add25af6990ac224
Quellennotizuspto-grants-2000_02