Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Aminopyridine → 2-(5-Bromo-2-fluorophenyl)-4-(4-pyridylamino)pteridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Aminopyridine | HCID 1727 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | PyBOP | HCID 2724699 | — |
| 반응물 | 2-(5-Bromo-2-fluoro-phenyl)-3H-pteridin-4-one | HCID 136109958 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(5-Bromo-2-fluorophenyl)-4-(4-pyridylamino)pteridine | HCID 11962218 | 32.9% |
반응 단계
Triethylamine (1.04 mL, 7.17 mmol) was added to a solution of 2-(5-bromo-2-fluoro-phenyl)pteridin-4-one 104 (800 mg, 2.49 mmol), 4-aminopyridine (469 mg, 4.98 mmol) and PyBOP (2.59 g, 4.98 mmol) in CH2Cl2. After 12 h, the reaction mixture was partitioned between CH2Cl2/Petroleum ether (2:1, 300 mL) and ice-cold 1N HCl (300 mL). The pH of the water phase was adjust to 12 with conc. NaOH and extracted with AcOEt, dried (Na2SO4) and evaporated. The residue was triturated in CH2Cl2/Petroleum ether (2:1, 15 mL), filtered off, and washed with ether. The product was purified by column chromatography (AcOEt/CH2Cl2/MeOH, 5:4:1) to give 325 mg of the title product 1 as a yellow powder (LCMS analysis).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09290502B2 |
| 출처 데이터셋 | uspto-grants-2016_03 |
| ORD ID | ord-e424538959524fd3a03095ac2cf1a4bf |
| 출처 메모 | uspto-grants-2016_03 |