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Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate → Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate | HCID 11601501 | — |
| 反応物 | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate | HCID 12795552 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04636509 |
| 出典データセット | uspto-grants-1987_01 |
| ORD ID | ord-b7e772985ec74490bbde9a2c4ef6b3cc |
| 出典メモ | uspto-grants-1987_01 |