Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Ethylpiperazine → 4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Ethylpiperazine | HCID 79196 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 4-Amino-3-nitrobenzaldehyde | HCID 13237703 | — |
| 촉매 | HCID 178460666 | HCID 178460666 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamine | HCID 55046395 | 34% |
반응 단계
To a stirred solution of 1-ethyl-piperazine (1.37 g, 12 mmol) in MeOH (30 mL) was added Ti(OiPr)4 (1.73 g, 6 mmol). Then the solution was stirred at room temperature for 15 min. Then 4-amino-3-nitro-benzaldehyde (Procedure 2F, steps a-b, 1.5 g, 9 mmol) in MeOH (10 mL) was added and the solution was stirred at room temperature overnight. Then NaBH4 (380 mg, 10 mmol) was added and the solution was stirred at room temperature for 1 hour. The solution was diluted with EtOAc and filtered. The filtrate was washed with water and brine, dried over anhydrous Na2SO4. Concentration gave product, which was purified by flash chromatography on silica to obtain the title compound (800 mg, yield: 34%). MS (ESI): 265 [M+H]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09434697B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-09b9e11eaef04abeafbfb647896bb2e2 |
| 출처 메모 | uspto-grants-2016_09 |