Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 1-Isobutyl-4-(5-nitro-pyridin-2-yl)-piperazine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1-(5-Nitropyridin-2-yl)piperazine | HCID 2928799 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 1-Isobutyl-4-(5-nitro-pyridin-2-yl)-piperazine | HCID 68406877 | — |
반응 단계
A mixture of 7 g (34 mmol) 1-(5-nitro-pyridin-2-yl)-piperazine (commercially available), 3.15 g (44 mmol) isobutytraldehyde, 10.7 g (50 mmol) sodium trisacetoxyborohydride in 140 ml THF and 3 ml acetic acid was stirred at room temperature for 16 h. After addition of 50 ml water, THF was removed under vacuum. The residue was taken up in 300 ml water and 400 ml ethyl acetate and made alkaline by addition of 2M aq. Na2CO3 solution. The mixture was afterwards extracted two times with 300 ml ethyl acetate each. The combined organic phases were washed two times with 200 ml water each, dried with MgSO4 and evaporated to dryness. The residue was used without further purification in the synthesis of intermediate 9. (m/e): 265.0 (MH+; 100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07528135B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-0772e6aed8594464b169c4b07f50916d |
| 출처 메모 | uspto-grants-2009_05 |