関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Bis(4-methoxybenzyl)amine | HCID 714952 | — |
| 反応物 | 5-Bromo-3-fluoro-N-methyl-2-nitroaniline | HCID 71652038 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-Bromo-N,N-bis-(4-methoxy-benzyl)-N'-methyl-2-nitro-benzene-1,3-diamine | HCID 118235376 | — |
反応手順
A mixture of bis-(4-methoxy-benzyl)-amine (346 mmol), 5-bromo-3-fluoro-N-methyl-2-nitroaniline (297 mmol) and Et3N (891 mmol) was stirred at 120° C. for 16 h. The mixture was then cooled. The crude was combined with another one obtained following the same procedure described above. The resulting mixture was diluted in EtOAc and washed (2×0.2 M HCl, H2O and sat. NaHCO3). The organic phase was dried (Na2SO4) and concentrated to afford the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09440929B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-77d2bf5a1eea489e882ac6cc015a40cc |
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| 出典メモ | uspto-grants-2016_09 |
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