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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41350Erstellt: 24. Oktober 2026

Cyanogen Bromide → Quinazolin-2-amine

https://huagongshe.com/de/reaction/41350

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanogen BromideHCID 10476—
EduktHydrate;hydrochlorideHCID 21885828—
Eduktethyl-N-(6-amino-2,3-dichlorobenzyl)glycineHCID 67080112—
EduktAnagrelideHCID 135409400—
LösungsmittelTolueneHCID 1140—
ProduktQuinazolin-2-amineHCID 178508286—

Reaktionsschritte

Commercially, as discussed in U.S. Pat. No. 5,801,245, and as shown in FIG. 1, anagrelide has been prepared as the hydrochloride monohydrate (compound IV) from the intermediate, ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine (compound I) either by reaction with cyanogen bromide in hot alcoholic solution, or, preferentially, by reaction with cyanogen bromide in an aprotic solvent such as toluene to give the iminoquinazoline intermediate (compound II), which is isolated and then reacted with a base in a hot solution of alcohol to form anagrelide base (compound III).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530651B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-16c12e29c27c4e31ace7baeccc73080c
Quellennotizuspto-grants-2013_09