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HRID 1449727作成日:2026年10月25日

Isopropylamine → 3,5-Dichloro-4-(1-methylethylamino)pyridazine

https://huagongshe.com/reaction/1449727

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropylamineHCID 6363—
反応物3,4,5-TrichloropyridazineHCID 70111—
溶媒TolueneHCID 1140—
生成物3,5-Dichloro-4-(1-methylethylamino)pyridazineHCID 10822136—

反応手順

A solution of 3,4,5-trichloropyridazine (9.2 g) and isopropylamine (16.5 g) in toluene (25 ml) is refluxed for 18 hr. Excess isopropylamine is removed by atmospheric distillation. The residual solution is cooled and diluted with dichloromethane and aqueous sodium hydroxide solution (5%). The phases are separated. The organic phase is washed with water and then with saline. The organic phase is dried over sodium sulfate and concentrated under reduced pressure to give a liquid which contains a mixture of isomeric products. The isomers are separated by flash chromatography on silica gel eluting with ether/hexane (30/70). The appropriate fractions are pooled and concentrated to give the desired isomer, NMR (CDCl3) 1.33, 4.59, 4.87 and 8.60δ; CMR (CDCl3) 24.2, 46.4, 117.1,139.3, 145.5 and 151.3 δ.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05599930
出典データセットuspto-grants-1997_02
ORD IDord-9adad594ddb14b948b0d17328d8fd0ca
出典メモuspto-grants-1997_02