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HRID 130322作成日:2026年10月26日

Hydrochloric Acid → 1-[4-(5-Cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochloride

https://huagongshe.com/reaction/130322

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VilazodoneHCID 6918314—
溶媒TetrahydrofuranHCID 8028—
生成物1-[4-(5-Cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochlorideHCID 67300892—

反応手順

3 g of 1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine is dissolved in 100 ml of tetrahydrofuran and 10 ml of 2N or concentrated hydrochloric acid. After stirring for 2 to 3 minutes suction filtration of the precipitated crystals is effected. Drying in vacuo at room temperature to constant weight leads to 1-[4-(5-cyanoindol-3-yl)butyl]4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochloride of Form XII which present the characteristic x-ray diffraction spectrum of FIG. 25.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381726B2
出典データセットuspto-grants-2008_06
ORD IDord-511e5f91ce274eab9b37c68ed3ef861f
出典メモuspto-grants-2008_06