Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(4-Methoxybenzyl)aniline → 6-chloro-N-(4-methoxybenzyl)-N-phenylimidazo[1,2-b]pyridazin-8-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(4-Methoxybenzyl)aniline | HCID 408377 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 8-Bromo-6-chloroimidazo(1,2-b)pyridazine | HCID 46835269 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-chloro-N-(4-methoxybenzyl)-N-phenylimidazo[1,2-b]pyridazin-8-amine | HCID 59624558 | 48% |
반응 단계
A solution of potassium t-butoxide in THF (4.73 mL, 4.73 mmol) was added dropwise to a solution of N-(4-methoxybenzyl)aniline (0.92 g, 4.3 mmol) in THF (10 mL) at 0° C. The solution was warmed to RT for 15 minutes, recooled to 0° C. and a solution of 8-bromo-6-chloroimidazo[1,2-b]pyridazine (1.0 g, 4.30 mmol) from Example 1, step 1b, in THF (10 mL) was added in rapidly. The solution was stirred at 0° C. for 30 minutes and then at RT for 30 minutes. The reaction solution was concentrated in vacuo. The resulting residue was purified by flash chromatography eluting with 10% ethyl acetate/heptane to provide 0.75 g (48%) of 6-chloro-N-(4-methoxybenzyl)-N-phenyl imidazo[1,2-b]pyridazin-8-amine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07723336B2 |
| 출처 데이터셋 | uspto-grants-2010_05 |
| ORD ID | ord-f872ebe5ab9e4bf3836232c9d4280063 |
| 출처 메모 | uspto-grants-2010_05 |