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HRID 1893744作成日:2026年10月27日

N-(3-methoxyphenyl)piperazine → 4-Quinazolineacetic acid, 8-fluoro-3,4-dihydro-2-[4-(3-methoxyphenyl)-1-piperazinyl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-, methyl ester

https://huagongshe.com/reaction/1893744

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-methoxyphenyl)piperazineHCID 81430—
反応物Methyl (2E)-3-{3-fluoro-2-[({[2-methoxy-5-(trifluoromethyl)phenyl]imino}methylene)amino]-phenyl}-2-propenoateHCID 86597232—
溶媒DichloromethaneHCID 6344—
生成物4-Quinazolineacetic acid, 8-fluoro-3,4-dihydro-2-[4-(3-methoxyphenyl)-1-piperazinyl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-, methyl esterHCID 11983691—

反応手順

700 mg (1.78 mmol) of methyl (2E)-3-{3-fluoro-2-[({[2-methoxy-5-(trifluoromethyl)phenyl]-imino}methylene)amino]phenyl}-2-propenoate (Example 18A), 341 mg (1.78 mmol) of 1-(3-methoxyphenyl)piperazine and a spatula tip of silica gel are stirred in 20 ml of dichloromethane at room temperature for one hour and then under reflux for 35 hours. The target compound is obtained after purification on silica gel (dichloromethane, dichloromethane/ethyl acetate 10:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08513255B2
出典データセットuspto-grants-2013_08
ORD IDord-834b5122324b4f47ad12fc11010b8409
出典メモuspto-grants-2013_08