Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate → Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl 5-(2-bromoacetyl)-2-hydroxybenzoate | HCID 11601501 | — |
| 반응물 | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | Methyl 5-(5-chloro-2-oxopyrimidin-1-yl)acetylsalicylate | HCID 12795552 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04636509 |
| 출처 데이터셋 | uspto-grants-1987_01 |
| ORD ID | ord-b7e772985ec74490bbde9a2c4ef6b3cc |
| 출처 메모 | uspto-grants-1987_01 |