Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 4-(2-(2-Pyridyl)ethynyl)quinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Triphenylphosphine Oxide | HCID 13097 | — |
| 반응물 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 반응물 | 1-(Pyridin-2-yl)-2-(quinolin-4-yl)ethanone | HCID 10933856 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 4-(2-(2-Pyridyl)ethynyl)quinoline | HCID 21992637 | 43.4% |
반응 단계
A mixture of triphenyphosphine oxide (5.56 g, 10 mmol) in 1,2-dichloroethane (30 mL) is cooled in an ice bath. Trifluoromethanesulfonic anhydride (1.57 mL, 10 mmol) is added dropwise over 15 min. To this mixture is added a solution of 1-(2-pyridyl)-2-(4-quinolyl)ethan-1-one (2.5 g, 10 mmol) in 1,2-dichloroethane (10 mL) and triethylamine (2.84 mL, 20 mmol). The ice bath is removed and the mixture heated at reflux for 16 h. The mixture is diluted with dichloromethane (100 mL) and washed with water (3×100 mL), dried (magnesium sulfate), filtered, concentrated in vacuo, and chromatographed on SiO2 (0 to 100% hexane in ethyl acetate) to yield 1 g of title compound as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087626B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-6a89cb4b4dfe40218f7f1ec5cf9e62e9 |
| 출처 메모 | uspto-grants-2006_08 |