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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2113469Erstellt: 25. Oktober 2026

Triethylamine → (3-Chloro-1H-indol-5-yl)-(4-isopropyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/2113469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-IsopropylpiperazineHCID 78013—
EduktLithium hydroxide, monohydrateHCID 168937—
EduktSodium BicarbonateHCID 516892—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt3-Chloro-1H-indole-5-carboxylic acid methyl esterHCID 21998728—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3-Chloro-1H-indol-5-yl)-(4-isopropyl-piperazin-1-yl)-methanoneHCID 6862202644%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of 1.05 g (5 mmol) 3-Chloro-1H-indole-5-carboxylic acid methyl ester and 1.05 g (25 mmol) LiOH.H2O in THF, methanol, water was stirred at 50° C. for 4 h. The mixture was evaporated to dryness and the corresponding acid was used without further purification in the subsequent step. 0.77 g (6 mmol) 1-(2-propyl)-piperazine, 2.4g (7.5 mmol) TBTU, 2.5 g (25 mmol) NEt3 and 20 mL DMF was added and the mixture was stirred at room temperature for 4 h. 1N NaHCO3 was added and the mixture was extracted with DCM. The combined organic layers were dried with MgSO4, filtered and evaporated. The residue was purified by flash column chromatography on silica eluting with a gradient formed from heptane, ethyl acetate, methanol and NEt3. The combined product fractions were evaporated to yield 0.67 g (44%) of the title compound as light brown solid. MS(m/e): 306.3 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07432255B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-7c4df635f0e34bab99499a35d4c8f42a
Quellennotizuspto-grants-2008_10