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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359726Erstellt: 25. Oktober 2026

Hydrochloric Acid → N,N-dimethyl 3-indolepyruvamide

https://huagongshe.com/reaction/359726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylamineHCID 674—
EduktIndole-3-pyruvic acidHCID 803—
EduktHCID 178418300HCID 178418300—
KatalysatorGoldHCID 23985—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel4-MethylmorpholineHCID 7972—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN,N-dimethyl 3-indolepyruvamideHCID 53877758—

Reaktionsschritte

A solution of 500 mg 3-indolepyruvic acid in 25 ml anhydrous tetrahydrofuran on an ice-salt bath, under argon atmosphere and under stirring was additioned in swift succession with: 400 mg hydroxybenzotriazole (HOBt) and 570 mg 1-(3-dimethylaminopropyl)-3-ethylcarbimdie.HCl (EDC.HCl). After dissolving and still maintaining the ice-salt bath, 240 mg dimethylamine.HCl were added dissolved in 10 ml anhydrous tetrahydrofuran and 325 microliters 4-methylmorpholine (NMM). The yellowish gold solution was maintained under stirring for one night, leaving the bath temperature to rise up to room temperature. The volume was then tripled adding CH2Cl2 and the organic solution was washed in sequence with 5% NaHCO3 (10×25 ml), saturated NaCl solution (3×25 ml), 5% KHSO4 (10×25 ml) and saturated NaCl solution up to neutrality. After standing for one night on anhydrous Na2SO4, this was filtered off, the mixture was purified by flash chromatography (silica gel, eluent CH2Cl2 25/n-propanol 1,5).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05002963
Quelldatensatzuspto-grants-1991_03
ORD IDord-0086fdaf794944df91060ca4940e1dca
Quellennotizuspto-grants-1991_03