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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 661902Erstellt: 25. Oktober 2026

1,2-Dichloroethane → 4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamide

https://huagongshe.com/reaction/661902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt1-MethylpiperazineHCID 53167—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt5-bromo-8-carbamoyl-9H-carbazole-2-carboxylic acidHCID 59375082—
Lösungsmitteldichloromethane tetrahydrofuran DMFHCID 86642945—
Produkt4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamideHCID 4683352276,1%

Reaktionsschritte

A suspension of 5-bromo-8-carbamoyl-9H-carbazole-2-carboxylic acid (Intermediate 49-1, 1.84 g, 4.97 mmol), EDC (1.334 g, 6.96 mmol), and HOBT (1.066 g, 6.96 mmol) in THF-DCM-DMF (4:1:1) (124 mL) was treated with 1-methylpiperazine (1.656 mL, 14.91 mmol) and the mixture was stirred at rt for 3 days. The mixture was concentrated and the residue was partitioned between DCM and NaHCO3 (aq). The organic phase was washed with brine, dried and concentrated to afford an oil. This was purified by column chromatography (DCM-2 M methanolic ammonia, 100:0 to 95:5 to 92.5:7.5). The resulting solid was suspended in EtOAc, collected by filtration and dried to provide 4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamide (1.57 g, 76%). 1H NMR (400 MHz, DMSO-d6) δ 11.83 (s, 1H) 8.57 (d, J=8.13 Hz, 1H) 8.20 (br. s., 1H) 7.84 (d, J=8.35 Hz, 1H) 7.79 (s, 1H) 7.56 (br. s., 1H) 7.42 (d, J=8.13 Hz, 1H) 7.22 (d, J=8.13 Hz, 1H) 3.30-3.70 (m, 4H) 2.19-2.39 (m, 4H) 2.16 (s, 3H). Mass spectrum m/z 415, 417 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084620B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-8523230392b840b5b5de5c2e8b7a95e6
Quellennotizuspto-grants-2011_12