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HRID 493695作成日:2026年10月26日

Hydrochloric Acid → HCID 178482540、化合物

https://huagongshe.com/reaction/493695

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物1-(3-((6-Chloro-2-naphthyl)sulfonyl)propionyl)piperazineHCID 23130883—
反応物HCID 178482537HCID 178482537—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178482540HCID 178482540121.4%

反応手順

A suspension of 1-(3-((6-chloro-2-naphthyl)sulfonyl)propionyl)piperazine (2.5 g) obtained in Example 3a), N-((2Z)-4-chloromethyl-3-methyl-1,3-thiazol-2(3H)-ylidene)-N-methylamine hydrochloride (2.2 g) and potassium carbonate (2.4 g) in DMF (50 mL) was mixed at 65° C. for 3 hours. The solvent was distilled off under reduced pressure, the residue was diluted with an aqueous potassium carbonate solution, and extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The product, which was obtained by the purification of the residue with a basic silica gel column, was dissolved in ethyl acetate. A solution of hydrogen chloride in ether was added thereto, and the mixture was concentrated and dried to give the title compound (2.4 g) as a colorless powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534887B2
出典データセットuspto-grants-2009_05
ORD IDord-3a3fbf0254c84df7ae80a04ae775c56e
出典メモuspto-grants-2009_05