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HRID 568311作成日:2026年10月27日

N-methylcyclopentanamine → N-(4-pyridazinyl)-N'-cyclopentyl-N'-methylurea

https://huagongshe.com/reaction/568311

反応式

関与物質

役割名称HCID仕込み量
反応物N-methylcyclopentanamineHCID 7020624—
反応物Phenyl pyridazin-4-ylcarbamateHCID 14099147—
溶媒TetrahydrofuranHCID 8028—
生成物N-(4-pyridazinyl)-N'-cyclopentyl-N'-methylureaHCID 20150035—

反応手順

A stirred solution of 2.0 grams of phenyl N-(4-pyridazinyl)carbamate (prepared as in Example 2, Step A) and 0.9 gram of N-cyclopentyl-N-methyl amine in tetrahydrofuran is heated under reflux for 18 hours. The reaction mixture is filtered and the filtrate concentrated under reduced pressure to a residue. The residue is purified by column chromatography on silica gel to yield N-(4-pyridazinyl)-N'-cyclopentyl-N'-methylurea.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04728355
出典データセットuspto-grants-1988_03
ORD IDord-4f364a08bbb1497aba4f90badbd625b0
出典メモuspto-grants-1988_03