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4,5-Dichloro-3-hydroxypyridazine → N-[3-(o-chlorophenoxy)-2-hydroxypropyl]-N'-[4-chloro-3-oxopyridaz-5-yl]-ethylenediamine hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4,5-Dichloro-3-hydroxypyridazine | HCID 73247 | — |
| 反応物 | 1-[(2-Aminoethyl)amino]-3-(2-chlorophenoxy)propan-2-OL | HCID 15580997 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-[3-(o-chlorophenoxy)-2-hydroxypropyl]-N'-[4-chloro-3-oxopyridaz-5-yl]-ethylenediamine hydrochloride | HCID 15580998 | 78% |
反応手順
4.9 g of N-[3-(o-chlorophenoxy)-2-hydroxy-propyl]-ethylenediamine ##STR15## are dissolved in 50 ml of ethanol. A solution of 3.3 g of 4,5-dichloropyridazin-3-one ##STR16## in 50 ml of ethanol is added to the above solution, and the mixture is then heated under reflux for 12 hours. The mixture is then concentrated in vacuo, the residue is digested with a little ethyl acetate and decanted off from the ethyl acetate, and the residue is finally recrystallised from ethanol. The N-[3-(o-chlorophenoxy)-2-hydroxypropyl]-N'-[4-chloro-3-oxopyridaz-5-yl]-ethylenediamine hydrochloride ##STR17## is thus obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04532239 |
| 出典データセット | uspto-grants-1985_07 |
| ORD ID | ord-a15f75c8df9f41408cae84706636688f |
| 出典メモ | uspto-grants-1985_07 |