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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44761Erstellt: 23. Oktober 2026

Ethyl orthopropionate → 1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanol

https://huagongshe.com/de/reaction/44761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl orthopropionateHCID 66995—
Edukt1,1,1-TrimethoxybutaneHCID 123512—
Edukt4-Chloro-3-nitroquinolineHCID 11275808—
Edukt4-Chloro-3-nitronaphthyridineHCID 12543213—
Edukt1-(Aminomethyl)cyclopropan-1-olHCID 12609623—
Edukt1-(2-Aminoethyl)cyclopropanolHCID 55285781—
Produkt1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanolHCID 57515495—

Reaktionsschritte

1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanol was prepared according to the general methods of Parts D through G of Example 84 using 1-(aminomethyl)cyclopropanol in lieu of 1-(2-aminoethyl)cyclopropanol in Part D, 4-chloro-3-nitronaphthyridine in lieu of 4-chloro-3-nitroquinoline in Part D, and trimethyl orthobutyrate in lieu of triethyl orthopropionate in Part F. The crude product was triturated with hot acetonitrile to provide a tan solid. Which was recrystallized from chloroform and hexanes and dried at 140° C. under vacuum to provide product as an off-white solid, mp 199-200° C. MS (ESI) m/z 298 (M+H)+; Anal. calcd for C16H19N5O: C, 64.63; H, 6.44; N, 23.55. Found: C, 64.32; H, 6.62; N, 23.67.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541438B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-63b69e7bbeda44119ec322bdaa6cb786
Quellennotizuspto-grants-2013_09