Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-(6-Chloro-3-nitro-2-pyridyl)-alanine methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,6-Dichloro-3-nitropyridine | HCID 85239 | — |
| 반응물 | Alanine methyl ester hydrochloride | HCID 2733257 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(6-Chloro-3-nitro-2-pyridyl)-alanine methyl ester | HCID 54223679 | 69.3% |
반응 단계
L-Alanine methyl ester hydrochloride (8.4 g, 0.06 mol) was dissolved in 100 ml of anhydrous N,N-dimethylformamide, and 16.6 ml (0.12 mol) of triethylamine were added. Subsequently, while stirring vigorously, 10.7 g (0.05 mol) of 2,6-dichloro-3-nitropyridine in 20 ml of anhydrous N,N-dimethylformamide were slowly added dropwise, during which the reaction temperature rose above 40° C. After a further 3 h at room temperature, the reaction mixture was poured into about 400 ml of ice-water, extracted three times with ethyl acetate, dried (sodium sulfate) and concentrated. After chromatography on silica gel (ethyl acetate/heptane=1:5 then 1:2), 9.0 g (69%) of compound A were isolated as a yellow oil,
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05424311 |
| 출처 데이터셋 | uspto-grants-1995_06 |
| ORD ID | ord-2bed1d3a2f1f4567a7156d2e388c0edc |
| 출처 메모 | uspto-grants-1995_06 |