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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21104Erstellt: 25. Oktober 2026

1-(2-Hydroxyethyl)piperazine → 4-Chloro-7-{5-[4-(2-hydroxyethyl)piperazin-1-ylcarbonyl]-1-methylindol-2-yl}isoindolinone

https://huagongshe.com/reaction/21104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Hydroxyethyl)piperazineHCID 7677—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt4-Chloro-7-(5-carboxy-1-methylindol-2-yl)isoindolinoneHCID 68492178—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Chloro-7-{5-[4-(2-hydroxyethyl)piperazin-1-ylcarbonyl]-1-methylindol-2-yl}isoindolinoneHCID 6848748370%

Reaktionsschritte

In a similar manner to Step 1 of Example 20, Compound 157 (20.0 mg, 0.0587 mmol) was dissolved in DMF (1 mL), and the solution was treated with EDCI (23 mg, 0.12 mmol), HOBT monohydrate (7.9 mg, 0.059 mmol) and 1-(2-hydroxyethyl)piperazine (31 mg, 0.24 mmol). The mixture was added with water and ethyl acetate and extracted with 1 mol/L hydrochloric acid. The aqueous layer was added with sodium carbonate to adjust the pH to 9 and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in chloroform, and the solution was added with hexane and stirred for 30 minutes. The solid was collected by filtration and washed with hexane, followed by drying under reduced pressure to obtain Compound 159 (18.5 mg, yield 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5f6354f3c19e49c0b1987e6e923596f9
Quellennotizuspto-grants-2010_06