化工社化工社 化学情報印刷レポート · 研究参考用
Carbon Tetrachloride → Benzenemethanamine, 2,5-dichloro-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Carbon Tetrachloride | HCID 5943 | — |
| 反応物 | Benzylamine | HCID 7504 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 2-Chloro-5-iodotoluene | HCID 4200996 | — |
| 反応物 | Phthalimide potassium salt | HCID 24194345 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Benzenemethanamine, 2,5-dichloro- | HCID 457600 | — |
| 生成物 | 2-Chloro-5-iodobenzylamine | HCID 11460882 | — |
反応手順
The various benzylamine derivatives used in this study, when not commercially available, were synthesized by the methods shown in FIG. 5. 2,5-Dichlorobenzylamine 64 and 2-chloro-5-iodobenzylamine 65 were prepared from the corresponding benzyl bromides. Compound 60 was prepared from 2-chloro-5-iodotoluene by bromination with N-bromosuccinimide in CCl4. Wilson et al., J. Med. Chem 1989, 32, 1057-1062. 60 and 61 were treated with potassium phthalimide in N,N-dimethylformamide at 60° C. to obtain compounds 62 and 63 as white solids in 95% yield. Deprotection with hydrazine gave 64 and 65 in 80% yield. Treu et al., Molecules 2002, 7, 743-750.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07825126B2 |
| 出典データセット | uspto-grants-2010_11 |
| ORD ID | ord-90cacdc0e5ea44a0be82d06ded280f36 |
| 出典メモ | uspto-grants-2010_11 |