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1,2,3-Trichlorobenzene → 2,3-Dichloro-6-nitrobenzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2,3-Trichlorobenzene | HCID 6895 | — |
| 反応物 | 2,3,4-Trichloronitrobenzene | HCID 28697 | — |
| 反応物 | HCID 178418546 | HCID 178418546 | — |
| 反応物 | HCID 178508181 | HCID 178508181 | — |
| 生成物 | 2,3-Dichloro-6-nitrobenzonitrile | HCID 2736020 | — |
反応手順
As shown below in the Examples, a preferred process is set forth for making 2-amino-5,6-dichloro-3,4-dihydroquinazoline from commercially available starting materials. In one process 1,2,3-trichlorobenzene is used as the starting material and is nitrated using, for example, nitric/sulfuric acids to form 1,2,3-trichloro-4-nitrobenzene. This compound is then reacted with a cyanating agent such as CuCN to form 2,3-dichloro-6-nitrobenzonitrile. The nitrile is then reacted under reducing conditions using for example B2H6 to form 2,3-dichloro-6-nitrobenzylamine HCl which is then reduced and reacted with CNX to form the desired compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06194420B1 |
| 出典データセット | uspto-grants-2001_02 |
| ORD ID | ord-ef58309f84144dda8660277dd5c84248 |
| 出典メモ | uspto-grants-2001_02 |