関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Pyridazine | HCID 9259 | — |
| 反応物 | Phenyl chloroformate | HCID 15891 | — |
| 反応物 | Aminopyridazine | HCID 230373 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Pyridazinyl carbamate | HCID 20239911 | — |
反応手順
The reaction of a haloformate, such as phenyl chloroformate, and a pyridazineamine generally is carried out by combining a slight excess of haloformate with the pyridazine in an organic solvent, such as pyridine or triethylamine, and stirring the mixture for about 1 to about 24 hours at a temperature of about 0° to about 30° C. The product of the reaction, a pyridazinyl carbamate, is generally isolated by acidifying the reaction mixture, for instance by the addition of a mineral acid, such as hydrochloric acid or sulfuric acid, and collecting by filtration the precipitate which forms. The carbamate normally needs no further purification, but if desired it can be crystallized from common solvents, such as benzene, acetone, ethyl acetate, and the like.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04604127 |
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| 出典データセット | uspto-grants-1986_08 |
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| ORD ID | ord-492eae2209534bc4af5cb4e1d76c9009 |
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| 出典メモ | uspto-grants-1986_08 |
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