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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30805Erstellt: 23. Oktober 2026

Diisopropylethylamine → N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide

https://huagongshe.com/de/reaction/30805

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Methylpiperidine-4-carbonyl chlorideHCID 436503—
Edukt2-Amino-4-chloropyridineHCID 581866—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A flask was flame dried and placed under a nitrogen atmosphere. 1-methylpiperidine-4-carbonyl chloride (1 eq) in anhydrous methylene chloride was added to the flask and brought to 0° C. To this was added the solution containing 4-chloropyridin-2-amine (1 eq), and diisopropylethylamine (5 eq) in anhydrous methylene chloride, which was stirred for 1 hour at 0° C. Reaction concentrated and partitioned between water and ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated to give the crude product. Purification on silica gel, 10% methanol in methylene chloride to yield N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide as a slightly yellow crystal solid. HPLC=2.39 min; MS: MH+=254.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423150B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-09769fb5fb4e43ffa1082f09d673b2a1
Quellennotizuspto-grants-2008_09