Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| 반응물 | 3-Amino-5-bromo-2-chloropyridine | HCID 21858354 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide | HCID 86658034 | — |
반응 단계
To a solution of 5-bromo-2-chloropyridine-3-amine (3.9 g, 18.9 mmol) and triethylamine (5.3 mL, 37.9 mmol) in tetrahydrofuran (60 mL) was added 2-nitrobenzoylchloride (2.49 mL, 18.9 mmol). The reaction was stirred for 24 hours. The reaction mixture was diluted with ethyl acetate (200 mL) and saturated aqueous sodium bicarbonate (60 mL). The organic layer was separated and washed with water (50 mL), brine (50 mL), dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude product was purified by flash chromatography (SiO2, 25% ethyl acetate in hexanes). The N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide was obtained as a yellow solid (1.5 g). LCMS [M+H]: 356.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08541407B2 |
| 출처 데이터셋 | uspto-grants-2013_09 |
| ORD ID | ord-ab89fc2dc2b24ffea8f46cdcfcbc29fa |
| 출처 메모 | uspto-grants-2013_09 |