HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chloroacetaldehyde → 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chloroacetaldehyde | HCID 33 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 2,4-Diamino-6-oxodihydropyrimidine | HCID 19967567 | — |
| Produkt | 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08372852B2 |
| Quelldatensatz | uspto-grants-2013_02 |
| ORD ID | ord-067ea87fcd8a4978adfd23af028b0ae6 |
| Quellennotiz | uspto-grants-2013_02 |