Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 527978Erstellt: 25. Oktober 2026

3-((Tert-butyldimethylsilyl)oxy)propanal → (RS)-1-[([3-(tert-butyl-dimethyl-silanyloxy)-propy]-{2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethyl}-amino)-methyl]-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-one

https://huagongshe.com/reaction/527978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—
Edukt(1RS)-9-fluoro-1-({2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethylamino}-methyl)-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 67348543—
Produkt(RS)-1-[([3-(tert-butyl-dimethyl-silanyloxy)-propy]-{2-[(S)-2-oxo-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-oxazolidin-5-yl]-ethyl}-amino)-methyl]-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-oneHCID 6713443287%

Reaktionsschritte

Starting from the compound of Example 4 and 3-(tert-butyldimethylsilyloxy)-propionaldehyde and using procedure E, the title compound was obtained as a yellow foam (82 mg; 87% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346804B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-b5c13323cddb46b1984cbfbe290d9f76
Quellennotizuspto-grants-2016_05