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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 386620Erstellt: 26. Oktober 2026

Chloroacetaldehyde → 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine

https://huagongshe.com/reaction/386620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetaldehydeHCID 33—
EduktBenzyl BromideHCID 7498—
EduktPhosphorus oxychlorideHCID 24813—
Edukt2,4-Diamino-6-oxodihydropyrimidineHCID 19967567—
Produkt7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amineHCID 10587340—

Reaktionsschritte

In some embodiments, condensation of 2,6-diamino-1,2-dihydro[3H]pyrimidin-4-one with chloroacetaldehyde, followed by treatment with phosphorus oxychloride and anime protection with benzyl bromide provides 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine. In some embodiments, this is coupled with optionally substituted (R1, R2, R3, R4) para-bromo phenol or thiol (T=O, S) or para-bromoaniline (T=NH). In some embodiments, conversion of amine to fluoro is achieved by treatment with HF-pyridine, and then coupled with para-V-aniline. In some embodiments, benzyl deprotection is achieved by treatment with aluminum chloride to give the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08372852B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-067ea87fcd8a4978adfd23af028b0ae6
Quellennotizuspto-grants-2013_02