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HRID 1194349作成日:2026年10月25日

Formaldehyde → 3-(Dimethylamino)-1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-propanone hydrochloride hemihydrate

https://huagongshe.com/reaction/1194349

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Dimethylamine, hydrochlorideHCID 10473—
反応物1-(5-Methoxy-1-methyl-1H-indol-3-yl)ethan-1-oneHCID 21270028—
溶媒EthanolHCID 702—
生成物3-(Dimethylamino)-1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-propanone hydrochloride hemihydrateHCID 70045959—

反応手順

A mixture of 1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-ethanone (0.23 g), paraformaldehyde (0.07 g) and dimethylamine hydrochloride (0.2 g) in ethanol (20 ml) was heated at reflux for 24 h, cooled, and the solvent was evaporated in vacuo. The residue was partitioned between sodium carbonate (2N; 50 ml) and ethyl acetate (2×50 ml). The combined organic extracts were dried and evaporated in vacuo to give an oil, which was purified by FCC eluting with System A to give the free base of the title compound as an oil. This was dissolved in absolute ethanol (5 ml) acidified with ethanolic hydrogen chloride, and the salt was precipitated by the addition of excess dry ether (100 ml). The salt was filtered off and dried in vacuo to give the title compound (0.1 g), m.p. 210°-211°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04814344
出典データセットuspto-grants-1989_03
ORD IDord-9b9d20f39774446f835bc8e0b6fc8660
出典メモuspto-grants-1989_03