HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34759Erstellt: 24. Oktober 2026
2-Chloroacrylonitrile → 4-Amino-2-(4-phthalimidobutyl)pyrimidine
https://huagongshe.com/de/reaction/34759
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Chloroacrylonitrile | HCID 70198 | — |
| Edukt | 1,5-Diazabicyclo(5,4,0)undec-5-ene | HCID 314112 | — |
| Edukt | 1-Amidino-4-phthalimidobutane hydrochloride | HCID 21298870 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-Amino-2-(4-phthalimidobutyl)pyrimidine | HCID 20450337 | 42,2% |
Reaktionsschritte
A solution of 2-chloroacrylonitrile (1.75 g.) in acetronitrile (10 ml.) was added over 15 minutes to an ice-cooled mixture of 1-amidino-4-phthalimidobutane hydrochloride (5.64 g.), acetonitrile (50 ml.) and 1,5-diazabicyclo[5,4,0]undec-5-ene (6.08 g.). The mixture was stirred for a further two hours and then evaporated to dryness. The residue was treated with water (50 ml.) and the mixture extracted with ethyl acetate (2×50 ml.). The combined ethyl acetate extracts were extracted with N hydrochloric acid (3×30 ml.) and the combined aqueous extracts neutralised with sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate extracts were evaporated to dryness and the residue recrystallised from acetonitrile to give 4-amino-2-(4-phthalimidobutyl)pyrimidine (2.5 g.), m.p. 139°-140°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04762932 |
|---|
| Quelldatensatz | uspto-grants-1988_08 |
|---|
| ORD ID | ord-440b1d3585c8494281a1602658ea97d9 |
|---|
| Quellennotiz | uspto-grants-1988_08 |
|---|