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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349293Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → 7-(2-Formyl-6-oxo-piperidin-1-yl)-hept-5-ynoic acid methyl ester

https://huagongshe.com/reaction/349293

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
Eduktpyridine TFAHCID 9813011—
Edukt7-(2-Hydroxymethyl-6-oxo-piperidin-1-yl)-hept-5-ynoic acid methyl esterHCID 69020340—
LösungsmittelBenzeneHCID 241—
Produkt7-(2-Formyl-6-oxo-piperidin-1-yl)-hept-5-ynoic acid methyl esterHCID 86012500—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1-(3-(Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI, 530 mg, 2.76 mmol) and DMSO (0.26 mL, 3.68 mmol) were added sequentially to a solution of 7-(2-hydroxymethyl-6-oxo-piperidin-1-yl)-hept-5-ynoic acid methyl ester (246 mg, 0.92 mmol) in benzene (7.0 mL) at rt. The mixture was cooled to 0° C. and pyridinium trifluoroacetate (196 mg, 1.01 mmol) was added. The reaction was allowed to warm to rt and then was stirred at rt for 2.5 h. The solution was decanted from the oily residue and the residue was washed with benzene (3×5 mL). The combined benzene phases were concentrated in vacuo to afford crude 7-(2-formyl-6-oxo-piperidin-1-yl)-hept-5-ynoic acid methyl ester that was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179820B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-5b34f265fd4543b1879cc269ea10dbe1
Quellennotizuspto-grants-2007_02