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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 734321Erstellt: 24. Oktober 2026

1,2-Dichloroethane → 1-Benzyl-4-(1-tert-butoxycarbonyl-piperidine-4-carbonyl)-[1,4]-diazepane

https://huagongshe.com/de/reaction/734321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-Benzyl-1,4-diazepaneHCID 228365—
Edukt1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Benzyl-4-(1-tert-butoxycarbonyl-piperidine-4-carbonyl)-[1,4]-diazepaneHCID 6035460389%

Reaktionsschritte

1-Benzyl-[1,4]-diazepane (3.78 g) and 1-tert-butoxycarbonyl-piperidine-4-carboxylic acid (5.0 g) were dissolved in DCM (150 ml) and TEA (3.6 ml) was added followed by HOBT (1.34 g) and finally EDC (4.90 g). The reaction was stirred at rt overnight. The reaction mixture was then evaporated to a minimum, re-dissolved in DCM (50 ml) and washed with saturated sodium hydrogen carbonate solution (3×50 ml) and brine (50 ml). The organic layer was dried (MgSO4) and evaporated to a crude which was purified by column chromatography [silica gel, step gradient 0-10% MeOH (containing 10% 0.880 ammonia solution) in DCM]. Fractions containing pure desired product were combined and evaporated to give the subtitled compound as a pale brown solid (7.1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592347B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-32171a7d5ee746c5a0b602b6bdb50f56
Quellennotizuspto-grants-2009_09