HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 1-(2,3-Dimethylimidazo[2,1-b][1,3]thiazol-5-yl)-3-phenylprop-2-en-1-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanone | HCID 21256502 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-(2,3-Dimethylimidazo[2,1-b][1,3]thiazol-5-yl)-3-phenylprop-2-en-1-ol | HCID 467098 | — |
Reaktionsschritte
A solution of 2,3-Dimethyl-α-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazole-5-methanone (FIG. D-2) (0.34 g) in 1:1 ethanol:THF (40 mL) was treated with a solution of NaBH4 (0.35 g) in ethanol (5 mL). The solution was reacted for 2.5 hours, evaporated in vacuo, and the residue was diluted with water. The precipitated 2,3-Dimethyl-α-(2-phenylethenyl)imidazo[2,1-b]thiazole-5-methanol (FIG. D-5) was extracted into ethyl acetate, the extract was dried and evaporated to a viscous residue. The residue was triturated with ethyl acetate to yield 2,3-Dimethyl-α-(2-phenylethenyl)imidazo[2,1-b]thiazole-5-methanol (FIG. D-5), 0.28 g, m.p. 149-151° after crystallization from acetonitrile.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06191124B1 |
| Quelldatensatz | uspto-grants-2001_02 |
| ORD ID | ord-192b789b89b84680bdc5e6522e121c9e |
| Quellennotiz | uspto-grants-2001_02 |