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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58337Erstellt: 25. Oktober 2026

1,1'-Carbonyldiimidazole → N3-(tert-butoxycarbonyl)-N3-methyl-N-[4-(triphenylphosphonio) butyl]-beta-alaninamide bromide

https://huagongshe.com/reaction/58337

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt3-(Methylamino)propanoic acid, N-BOC protectedHCID 2760952—
Edukt(4-Aminobutyl)(triphenyl)phosphonium bromideHCID 10201848—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktN3-(tert-butoxycarbonyl)-N3-methyl-N-[4-(triphenylphosphonio) butyl]-beta-alaninamide bromideHCID 131737008116,1%

Reaktionsschritte

N-(tert-butoxycarbonyl)-N-methyl-β-alanine (Matrix Scientific, 368 mg, 1.81 mmol) was dissolved in N,N-dimethylformamide (3.7 mL) and treated with N,N-carbonyldiimidazole (308 mg, 1.90 mmol). The reaction mixture was stirred at room temperature for 30 minutes. (4-Aminobutyl)(triphenyl)phosphonium bromide (1.12 g, 2.72 mmol) was added, and the reaction was stirred overnight at room temperature. The reaction was then diluted with methylene chloride and washed with 5% aqueous lithium chloride (3 times), 1N aqueous hydrogen chloride, and saturated sodium bicarbonate. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (1.26 g, 100%, 86% pure) as a white foam. Sample was used crude in next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434753B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-cdb50267135e41e7bd059917746c5047
Quellennotizuspto-grants-2016_09