HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenol → (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl Ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride | HCID 21249497 | — |
| Edukt | (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid | HCID 54200705 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl Ester | HCID 54508713 | — |
Reaktionsschritte
A solution of 1.30 g (5 mmols) (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid, 1.27 g (5 mmols) N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride, 0.49 g (5.2 mmols) phenol, and 1.10 g (10 mmols) triethylamine, in 10 ml dichloromethane was stirred at room temperature, under nitrogen atmosphere for 18 hours. Then, 10 ml of water (made slightly basic with sodium bicarbonate) were added. The precipitate was filtered of and the filtrate was dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. The residual orange-yellow solid was recrystallized from anhydrous ethanol. Yield--0.62 g. Mp 194°-195° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04588812 |
| Quelldatensatz | uspto-grants-1986_05 |
| ORD ID | ord-9bc3fb30f72f49fa81b82afc6e70df78 |
| Quellennotiz | uspto-grants-1986_05 |