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HRID 363987作成日:2026年10月27日

Pyridine → Pyridazinyl carbamate

https://huagongshe.com/reaction/363987

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物PyridazineHCID 9259—
反応物Phenyl chloroformateHCID 15891—
反応物AminopyridazineHCID 230373—
溶媒TriethylamineHCID 8471—
生成物Pyridazinyl carbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04604127
出典データセットuspto-grants-1986_08
ORD IDord-492eae2209534bc4af5cb4e1d76c9009
出典メモuspto-grants-1986_08