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HRID 2376759作成日:2026年10月27日

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 4,6-Diphenyl-2-(2-phthalimidoethyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/2376759

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
反応物4,6-diphenyl-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridineHCID 67014853—
生成物4,6-Diphenyl-2-(2-phthalimidoethyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridineHCID 6701408331%

反応手順

Following a similar procedure to that described in examples 6 and 7, but using 4,6-diphenyl-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine (obtained in example 2) instead of 4,6-bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine and N-(2-bromoethyl)phthalimide instead of iodoethane, the title compound was obtained (yield: 31%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07468376B2
出典データセットuspto-grants-2008_12
ORD IDord-fe5aa93613964648bc6cdb15e49bc365
出典メモuspto-grants-2008_12