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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 914929Erstellt: 24. Oktober 2026

(4-Methoxyphenyl)boronic acid → Formic acid;7-(4-methoxyphenyl)-2-methyl-4-pyrrolidin-1-ylquinazoline

https://huagongshe.com/de/reaction/914929

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Methoxyphenyl)boronic acidHCID 201262—
Edukt7-Bromo-2-methyl-4-pyrrolidin-1-yl-quinazolineHCID 22474939—
EduktHCID 68454173HCID 68454173—
KatalysatorHCID 178478475HCID 178478475—
LösungsmittelEthanolHCID 702—
ProduktFormic acid;7-(4-methoxyphenyl)-2-methyl-4-pyrrolidin-1-ylquinazolineHCID 8658510435%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a solution of 44 mg (0.15 mmol) 7-Bromo-2-methyl-4-pyrrolidin-1-yl-quinazoline in 1.2 ml dioxane/dimethoxyethane 1:1 was added 57 mg (0.375 mmol) 4-methoxy-phenyl-boronic acid in 0.4 ml ethanol, 7 mg (0.007 mmol) Dichloro[1,1′-Bis(diphenylphosphino)-ferrocene]-palladium (II) dichloromethan adduct, and 0.6 ml 2 M Na2CO3aq. and the mixture was heated to 85° C. for 12 h. After filtration, the mixture was purified by reversed phase column chromatography eluting with an acetonitrile/water (formic acid) gradient yielding 17 mg (35%) of the title compound. MS m/e (%): 320.4 (M+H+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265125B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-5832632b41374174addb484f008674ce
Quellennotizuspto-grants-2007_09