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o-CRESYL GLYCIDYL ETHER → 1-(2-Methylphenoxy)-3-[1,1-dimethyl-3-(chloro-6-pyridazinyloxy)propylamino]-2-propanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | o-CRESYL GLYCIDYL ETHER | HCID 16640 | — |
| 反応物 | 3-(3-Amino-3-methylbutoxy)-6-chloropyridazine | HCID 10036235 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(2-Methylphenoxy)-3-[1,1-dimethyl-3-(chloro-6-pyridazinyloxy)propylamino]-2-propanol | HCID 10362358 | 82.6% |
反応手順
A mixture of 645 mg of 3-(3-amino-3-methylbutoxy)-6-chloropyridazine, 650 mg of 1-(2-methylphenoxy)-2,3-epoxypropane and 15 ml of methanol was refluxed for 5 hours, and the solvent was evaporated under reduced pressure. A solution of the residue in benzene was extracted with 1N hydrochloric acid. The aqueous layer was extracted with chloroform, and the organic layer was washed with 5% sodium carbonate, and dried over anhydrous sodium sulfate. The solvent was evaporated to give 938 mg of 1-(2-methylphenoxy)-3-[1,1-dimethyl-3-(chloro-6-pyridazinyloxy)propylamino]-2-propanol as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04599333 |
| 出典データセット | uspto-grants-1986_07 |
| ORD ID | ord-e53fe69f9f624a768ba47b67fbbb6b00 |
| 出典メモ | uspto-grants-1986_07 |