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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372760Erstellt: 26. Oktober 2026

6-Fluoro-1-methyl-1H-indole-3-carbaldehyde → Methyl (2-(6-fluoro-1-methyl-3-indolyl)-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Fluoro-1-methyl-1H-indole-3-carbaldehydeHCID 6498197—
EduktIodo benzene diacetateHCID 12217721—
EduktMethyl 2-(4-amino-3-hydroxyphenyl)acetateHCID 17858854—
LösungsmittelEthanolHCID 702—
ProduktMethyl (2-(6-fluoro-1-methyl-3-indolyl)-6-benzoxazolyl)acetateHCID 5877843093,2%

Reaktionsschritte

In ethanol (15 ml), 6-fluoro-1-methylindole-3-carbaldehyde (500 mg, 2.82 mmol) and methyl 4-amino-3-hydroxyphenylacetate (767 mg, 4.23 mmol) were stirred at room temperature for 2 hours. Iodobenzene diacetate (1.09 g, 3.38 mmol) was added and the mixture was stirred at room temperature for 1 hour. The reaction mixture was then distilled under reduced pressure to remove the solvent. The residue was purified chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (1:1, v/v) eluate fractions, methyl (2-(6-fluoro-1-methyl-3-indolyl)-6-benzoxazolyl)acetate (889 mg, 93%) was obtained as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157487B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-97a2e736cd95465483e564c7eb34cdf4
Quellennotizuspto-grants-2007_01