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HRID 215916作成日:2026年10月25日

3-Piperidinecarboxamide → 1-(4-(1-(2-(Dimethylamino)-6-methoxybenzyl)piperidin-4-ylamino)quinazolin-2-yl)piperidine-3-carboxamide

https://huagongshe.com/reaction/215916

反応式

関与物質

役割名称HCID仕込み量
反応物3-PiperidinecarboxamideHCID 92980—
反応物2-Chloro-N-(1-(2-(dimethylamino)-6-methoxybenzyl)piperidin-4-yl)quinazolin-4-amineHCID 58006255—
溶媒1,4-DioxaneHCID 31275—
生成物1-(4-(1-(2-(Dimethylamino)-6-methoxybenzyl)piperidin-4-ylamino)quinazolin-2-yl)piperidine-3-carboxamideHCID 58006197—

反応手順

Compound 47 (50 mg, 0.12 mmol) and piperidine-3-carboxamide (45 mg, 0.36 mmol) in 1,4-dioxane (5 mL) were heated to 117° C. for 24 h in a sealed tube. The product (AGN-219171) was purified by basic alumina flash column chromatography using 3% MeOH and 97% CH2Cl2 solution as eluent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193203B2
出典データセットuspto-grants-2012_06
ORD IDord-6b7548b5b5d144a5b7d79804b8cda90a
出典メモuspto-grants-2012_06