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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 874875Erstellt: 23. Oktober 2026

Aniline → 3-(3-chloro-phenyl)-5-methyl-2-[1-(9H-purin-6-ylamino)-ethyl]-3H-quinazolin-4-one

https://huagongshe.com/de/reaction/874875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktTrifluoroacetic acidHCID 6422—
Edukt3-ChloroanilineHCID 7932—
EduktSuccinimido (S)-2-((tert-butoxycarbonyl)amino)propionateHCID 100126—
Edukt(2,5-Dioxopyrrolidin-1-yl) 2-(phenylmethoxycarbonylamino)butanoateHCID 12961228—
Edukt2-[1-(2-amino-9H-purin-6-ylamino)-ethyl]-3-(3-methylphenyl)-5-methyl-3H-quinazolin-4-oneHCID 178425448—
EduktHCID 178456854HCID 178456854—
Produkt3-(3-chloro-phenyl)-5-methyl-2-[1-(9H-purin-6-ylamino)-ethyl]-3H-quinazolin-4-oneHCID 178423952—

Reaktionsschritte

Compound 66 was prepared using the general procedure described above with respect to compound 14, but 3-chloroaniline was substituted for aniline in step A, 2-tert-butoxycarbonylamino-propionic acid 2,5-dioxopyrrolidin-1-yl ester was substituted for 2-benzyloxycarbonylaminobutyric acid 2,5-dioxo-pyrrolidin-1-yl ester in step B, and the alternate procedure (TFA deprotection) was used in step C. 1H NMR (dmso-d6): 8.40-8.31 (m, 2H); 7.73-7.66 (m, 1H); 7.55-7.32 (m, 6H); 5.04-4.86 (m, 1H); 2.72 (s, 3H); 1.52-1.50 (m, 3H). Compound 65 is shown below.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08980901B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-d2d34b31afff45afab776cc95c4d365a
Quellennotizuspto-grants-2015_03