HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4,5-Dihydro-2-thiazolamine → 2,3,8,9-Tetrahydro-5-(4-methoxy-2,5-dimethylphenyl)-9-[(4-methoxy-2,5-dimethylphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4,5-Dihydro-2-thiazolamine | HCID 15689 | — |
| Edukt | Tetrahydro-3,5-bis[(4-methoxy-2,5-dimethylphenyl)methylene]-4H-pyran-4-one | HCID 53782418 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 2,3,8,9-Tetrahydro-5-(4-methoxy-2,5-dimethylphenyl)-9-[(4-methoxy-2,5-dimethylphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidine | HCID 21786682 | 46,9% |
Reaktionsschritte
A stirred solution of tetrahydro-3,5-bis[(4-methoxy-2,5-dimethylphenyl)methylene]-4H-pyran-4-one (3.0 g, 7.6 mmole) and 2-amino-2-thiazoline (1.0 g, 9.7 mmole) in 75 ml of CHCl3 is heated at reflux temperature for 72 hours. After cooling, the solution is filtered to remove a small amount of insoluble material. The solvent is evaporated to give an oily residue. A solution of this material in 25 ml of EtOH yields 1.7 g of light yellow solid, m.p. 195°-197°. Crystallization from 20 ml of 10% DMF/MeOH gives 1.3 g (35%) of cream colored solid, m.p. 196°-198°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04128648 |
| Quelldatensatz | uspto-grants-1978_12 |
| ORD ID | ord-f8d52a0270014774bde0a6d1b66b7a76 |
| Quellennotiz | uspto-grants-1978_12 |