Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Phenacyl bromide → HCID 11393000, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Phenacyl bromide | HCID 6259 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-(1H-benzimidazol-2-yl)-1,2,5-oxadiazol-3-amine | HCID 738531 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | HCID 11393000 | HCID 11393000 | — |
반응 단계
Phenacylbromid (0.1 g, 0.49 mmol) is added to an efficiently stirred suspension of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.1 g, 0.4 mmol) [A. V. Sergievskii, O. A. Krasnoshek, S. F. Mel'nikova, I. V. Tselinskii, Russian Journal of Organic Chemistry, 2002, 38, 915-917] and potassium carbonate (0.172 g, 1.24 mmol) in dry DMF (5 ml) at room temperature. After 4 hours the reaction mixture is diluted with ethyl acetate and the organic phase is washed repeatedly with brine. Drying of the solvent, filtering and evaporation of the solvent under reduced pressure gives the title compound in crude form. The title compound is obtained in pure form by chromatography over silicagel, m.p. 202-204° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | USRE042890E1 |
| 출처 데이터셋 | uspto-grants-2011_11 |
| ORD ID | ord-3183b4f3c424424c9aae9d495ef6789c |
| 출처 메모 | uspto-grants-2011_11 |