Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245689Erstellt: 25. Oktober 2026

1-Carbobenzoxy-4-piperidinecarboxylic Acid → Benzyl 4-((3-chloropyrazin-2-yl)methylcarbamoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/245689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
EduktBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
Edukt(3-Chloropyrazin-2-yl)methanamine hydrochlorideHCID 42614233—
ProduktBenzyl 4-((3-chloropyrazin-2-yl)methylcarbamoyl)piperidine-1-carboxylateHCID 4260936683,4%

Reaktionsschritte

Using the procedures described in example 16 step 16a 1-[(benzyloxy)carbonyl]piperidine-4-carboxylic acid (2.5 g) was transformed into 2.75 g of crude benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate and the latter compound was coupled with 2-aminomethyl-3-chloropyrazine hydrochloride (content 77%; 2.28 g) to give benzyl 4-((3-chloropyrazin-2-yl)methylcarbamoyl)piperidine-1-carboxylate (3.08 g) after purification by column chromatography (silica gel, dichloromethane/methanol gradient 100/0 to 90/10).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658794B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-a03bbc317db548afb1f4ea8da646b2e7
Quellennotizuspto-grants-2014_02