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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 428564Erstellt: 23. Oktober 2026

Acetic Acid → HCID 178480352, Verbindung

https://huagongshe.com/de/reaction/428564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanoneHCID 18414059—
Edukt6-Bromo-8-piperazin-1-yl-quinolineHCID 18414063—
Lösungsmittel1,1-DichloroethaneHCID 6365—
ProduktHCID 178480352HCID 178480352—

Reaktionsschritte

To a solution of 6-bromo-8-piperazin-1-yl-quinoline (610 mg, 2.09 mmol), 4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanone (510 mg, 2.09 mmol), and sodium triacetoxyborohydride (660 mg, 3.14 mmol) in dichloroethane (40 mL) was added acetic acid (0.24 mL, 4.18 mmol) and stirred overnight at room temperature. The reaction was quenched with 1 M NaOH (50 mL) and H2O (100 mL) then extracted in CH2Cl2 (100 mL) and EtOAc (100 mL). The organic fractions were combined, dried over Na2SO4, concentrated, filtered and chromatographed (5% MeOH/EtOAc). The majority of the cis compound precipitated out of 5% MeOH/EtOAc before application to the column and was purified by filtration affording 510 mg (47%) of the cis isomer as a pale yellow solid: mp 215-217° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313126B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-80d4d186d76f4258b0f6708d2ff5d583
Quellennotizuspto-grants-2001_11