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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 403411Erstellt: 23. Oktober 2026

Ethyl Acetate → (2S,4R)-tert-butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate

https://huagongshe.com/de/reaction/403411

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktDiisopropylethylamineHCID 81531—
Edukt(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
EduktVinylcyclopropylammonium tosylateHCID 86664338—
Produkt(2S,4R)-tert-butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 57892908—

Reaktionsschritte

To a stirring slurry of N-Boc-hydroxy proline (78 g), HATU (128 g), and EtOAc (558 g), at 0° C., was added diisopropylethylamine (65 g). After 45 min, a solution containing vinylcyclopropylammonium tosylate (100 g), diisopropylethylamine (65.0 g), and EtOAc (366 g) was added to the activated ester solution. After 3 h at 10° C., the reaction slurry was filtered and the resulting cake was rinsed with EtOAc (1.8 kg). The resulting filtrate was washed with a 10% aqueous solution of NaCl (5×770 g). The product-containing organic layer was filtered, concentrated under reduced pressure, diluted with EtOAc (450 g), and then filtered again. The assay yield of the final product-containing solution was determined to be 85%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08748374B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-6e8f21d4648b464387d51f17acace3f5
Quellennotizuspto-grants-2014_06