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HRID 568303作成日:2026年10月27日

Cyclopentylamine → N-(4-pyridazinyl)-N'-cyclopentylurea

https://huagongshe.com/reaction/568303

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentylamineHCID 2906—
反応物Phenyl pyridazin-4-ylcarbamateHCID 14099147—
溶媒TetrahydrofuranHCID 8028—
生成物N-(4-pyridazinyl)-N'-cyclopentylureaHCID 1409914910.8%

反応手順

A stirred solution of 2.0 grams (0.009 mole) of phenyl N-(4-pyridazinyl)carbamate and 1.0 ml (0.010 mole) of cyclopentylamine 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. Elution is accomplished with 10% methanol in methylene chloride. The appropriate fractions are combined and concentrated under reduced pressure to yield 0.2 gram of N-(4-pyridazinyl)-N'-cyclopentylurea. This material is combined with the identical product from a previous reaction to yield 0.5 gram; m.p. 192°-195° C., dec. The nmr spectrum is consistent with the proposed structure. The reaction is repeated several times.

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-72751b774d7d4e85889ba395ee64ee29
出典メモuspto-grants-1988_03