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HRID 902197作成日:2026年10月26日

Acetonitrile → HCID 178482579、化合物

https://huagongshe.com/reaction/902197

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物3,3-DiphenylacroleinHCID 71027—
反応物9-AminominocyclineHCID 54676112—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物HCID 178482579HCID 17848257997.1%

反応手順

9-aminominocycline sulfate salt (0.500 g, 0.748 mmol) is dissolved in anhydrous DMF and treated with β-phenylcinnamaldehyde (0.779 g, 3.74 mmol, 5 equivalents) The solution is then treated with DDQ (0.085 g, 0.374 mmol, 0.5 equivalents) and stirred at room temperature for 5 min. ES+ mass spectrometry showed a 1:1 ratio of product and starting material. A second portion of DDQ (0.068 g, 0.300 mmol, 0.4 equivalents) is added. After approximately 5 minutes, acetonitrile (7.5 mL) is added, and the entire reaction mixture is poured slowly into ether (750 mL.) The pink solid is removed by filtration and washed with fresh ether to yield 0.480 g of the crude product. This material is dissolved in water (75 mL) to give a solution at pH 2.2, which is extracted with dichloromethane (2×100 mL.) The pH of the aqueous layer is raised to 3.0 with aqueous ammonia, and the solution is again extracted with dichloromethane (2×100 mL.) The four organic extracts are dried (Na2SO4), filtered and concentrated to a volume of about 2 mL. A small portion of methanol (1 mL) is added, and the concentrated solution is treated dropwise with 1M HCl in ether. The solid precipitate is filtered, washed with fresh ether and dried under vacuum the product as its HCl salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365087B2
出典データセットuspto-grants-2008_04
ORD IDord-7db64fe582f040dfbc10e4ea06ba3808
出典メモuspto-grants-2008_04