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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1430730Erstellt: 26. Oktober 2026

Nicotinic Acid → Tert-butyl 2-(nicotinamido)ethylcarbamate

https://huagongshe.com/reaction/1430730

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNicotinic AcidHCID 938—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktN-BOC-ethylenediamineHCID 187201—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 2-(nicotinamido)ethylcarbamateHCID 4745332874%

Reaktionsschritte

In a typical run, nicotinic acid (2.0 g, 16.2 mmol) was taken up in CH2Cl2 (20 mL) along with oxalyl chloride (1.4 mL, 16.2 mmol). After a few drops of DMF were added, the reaction mixture was stirred at room temperature until all the solids had dissolved and all gas evolution had ceased (1 h). This freshly prepared solution of the acid chloride was added dropwise at 0° C. to a solution containing tert-butyl 2-aminoethylcarbamate (2.6 g, 16.2 mmol) and Et3N (3.4 mL, 24.2 mmol) in CH2Cl2 (200 mL). The resulting reaction mixture was warmed to room temperature and stirred for 2 h. It was then washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by silica gel chromatography (CH2Cl2) afforded tert-butyl 2-(nicotinamido)ethylcarbamate (3.1 g, 74%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08940903B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-673eac003ba94bcb9b77b863510ceb5f
Quellennotizuspto-grants-2015_01