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HRID 1081272作成日:2026年10月27日

1-Bromo-2-Chloroethane → 1-(2-chloroethyl)-5,6-dimethoxy-1H-indole-2,3-dione

https://huagongshe.com/reaction/1081272

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-ChloroethaneHCID 7849—
反応物Potassium CarbonateHCID 11430—
反応物5,6-dimethoxy-2,3-dihydro-1H-indole-2,3-dioneHCID 4739148—
溶媒DimethylformamideHCID 6228—
生成物1-(2-chloroethyl)-5,6-dimethoxy-1H-indole-2,3-dioneHCID 23363882—

反応条件

温度70 °C

反応手順

Anhydrous potassium carbonate (2.44 g) was added to a solution of 5,6-dimethoxy-1H-indole-2,3-dione (1.2 g) in dry DMF (5 ml). 2-Bromo-1-chloroethane (4.1 g) was added and the mixture was heated at 70° C. for 2 hours. The mixture was evaporated to dryness under reduced pressure and the residue was purified by flash chromatography on silica gel. The 1-(2-chloroethyl)-5,6-dimethoxy-1H-indole-2,3-dione thus obtained was dissolved in dry DMF (5 ml) and anhydrous potassium carbonate (2.44 g), potassium iodide (100 mg) and 1-(phenylmethyl)piperazine (3.06 g) were added. The mixture was stirred and heated at 70° C. for 2 hours and then evaporated to dryness under reduced pressure. The residue was purified by chromatography to yield a red oil which on treatment with ethanolic HCl afforded 5,6-dimethoxy-1-[2-[4-(phenylmethyl)-1-piperazinyl]ethyl]-1H-indole-2,3-dione dihydrochloride (33%), m.p. 205°-207° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05585378
出典データセットuspto-grants-1996_12
ORD IDord-80dc03e70e0c4676ae16fdc3867da439
出典メモuspto-grants-1996_12