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Acetylacetone → 6-Bromo-2-methyl-4-nitro-1H-benzo[d]imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetylacetone | HCID 31261 | — |
| 反応物 | 5-Bromo-3-nitrobenzene-1,2-diamine | HCID 45789403 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Bromo-2-methyl-4-nitro-1H-benzo[d]imidazole | HCID 66976770 | 90% |
反応手順
A mixture of 5-bromo-3-nitrobenzene-1,2-diamine (464 mg) and pentane-2,4-dione (400 mg) in EtOH (27 mL) and 5 N HCl (7.4 mL) was refluxed for 3 h. The mixture was cooled to room temperature and the solvent was removed in-vacuo. The residue was dissolved in EtOAc and washed with aqueous NaHCO3 solution and brine. The organic layer was concentrated to afford the desired product as a solid (460 mg, 90%). 1H NMR (300 MHz, CDCl3) δ ppm 2.73 (s, 3H), 8.11 (d, 1H, J=1.8 Hz), 8.24 (d, 1H, J=1.8 Hz), 10.20 (s, 1H, s); LC-MS: m/e=256 [M+1]+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08541411B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-8db289205d6e4a8c89958eb31095a8e8 |
| 出典メモ | uspto-grants-2013_09 |