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HRID 22351作成日:2026年10月25日

Potassium Carbonate → 2,3-dihydro-8-{3-[4-(2-hydroxyphenyl)-1-piperazinyl]propoxy}-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/reaction/22351

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物o-(1-Piperazinyl)phenol dihydrobromideHCID 3017100—
反応物FumarateHCID 5460307—
反応物8-(3-chloropropoxy)-2,3-dihydro-7-methoxycyclopenta[c][1]benzopyran-4(1H)-oneHCID 19927690—
溶媒AcetoneHCID 180—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物2,3-dihydro-8-{3-[4-(2-hydroxyphenyl)-1-piperazinyl]propoxy}-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992769954%

反応手順

Method A (40 h at 50° C.; 4 equivalents of potassium carbonate); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(2-hydroxyphenyl)piperazine dihydrobromide; yield 54%; fusion point 136°-139° C. (from chloroform and ethanol). Fumarate: method E; yield 84%; fusion point 196°-199° C. (from acetone).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428038
出典データセットuspto-grants-1995_06
ORD IDord-ee7f6800e5e340bb926d02bf5856a982
出典メモuspto-grants-1995_06