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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611539Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 4-[4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopent-2-enol

https://huagongshe.com/de/reaction/611539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktCyclopentadieneHCID 7612—
Edukt5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamineHCID 12042234—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopent-2-enolHCID 22736320—

Reaktionsschritte

A mixture of 5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine (600 mg) and tetrakis(triphenylphosphine) palladium (40 ml) and dry dimethyl sulphoxide (30 ml) was stirred under nitrogen in an ice/water bath and then a solution of cyclopentadiene monoepoxide (200 mg) in tetrahydrofuran (10 ml) was added via syringe under nitrogen at 0° C. The mixture was stirred at ambient temperature for 66 hours and then the tetrahydrofuran was removed under reduced pressure and water was added to the residue. The mixture was allowed to stand for 18 hours and then extracted with ethyl acetate to give a residue which was purified by flash column chromatography on silica using ethyl acetate/industrial methylated spirit (9:1) as the mobile phase to give 4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopent-2-enol, as an oil. The structure was confirmed by 1Hnmr and mass spectra.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06001839
Quelldatensatzuspto-grants-1999_12
ORD IDord-e9c3f2a7f07f44d0826af43dc1643a1f
Quellennotizuspto-grants-1999_12