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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 369398Erstellt: 25. Oktober 2026

Acetic Anhydride → N-{2-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]pyridin-5-yl}-acetamide

https://huagongshe.com/reaction/369398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktMethyl 1-methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetateHCID 118468—
Edukt{2-[5-(4-Chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]pyridin-5-yl}amineHCID 15870202—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-{2-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]pyridin-5-yl}-acetamideHCID 5377608988%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of N-{2-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]pyridin-5-yl} amine (0.3 g, 0.88 mmol) [prepared by the method described in Example 5, but substituting zomepirac methyl ester for tolmetin methyl ester in Step (a)] and acetic anhydride (0.375 ml, 3.96 mmol) in THF was stirred at 60° C. for 4 h. The solvents were removed under reduced pressure and the residue was crystallized from hexane-chloroform to give N-{2-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-ylmethyl]pyridin-5-yl}-acetamide (295 mg, 88%) as a solid, mp 194-195° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06136844
Quelldatensatzuspto-grants-2000_10
ORD IDord-bc0f24cfd8ec4f79b687c2b913ae2263
Quellennotizuspto-grants-2000_10