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HRID 42601作成日:2026年10月24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/ja/reaction/42601

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US08536194B2
出典データセットuspto-grants-2013_09
ORD IDord-04e337fc91c94a5184a2716db9c83c69
出典メモuspto-grants-2013_09