HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate → Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate | HCID 11601501 | — |
| Edukt | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate | HCID 12795552 | — |
Reaktionsschritte
A solution of 5-chloropyrimidin-2-one hydrochloride (508 mg) and methyl 5-bromoacetylsalicylate (827 mg) in triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for 13/4 hours, by which time a precipitate had formed. This suspension was chilled in ice, and the collected solid was crystallised from chloroform-ethanol to give the title pyrimidinone: yield 442 mg: m.p. 203°-204° dec: λmaxEtOH 228.5 nm (ε 40720), 269.5 nm (ε 16930), 312.5 nm (ε 6320).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04636509 |
| Quelldatensatz | uspto-grants-1987_01 |
| ORD ID | ord-b7e772985ec74490bbde9a2c4ef6b3cc |
| Quellennotiz | uspto-grants-1987_01 |