戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 500841作成日:2026年10月26日

(7-Chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone → (7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/reaction/500841

反応式

関与物質

役割名称HCID仕込み量
反応物(7-Chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanoneHCID 11173165—
反応物7-(2-fluoro-4-nitrophenoxy)-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamideHCID 59424475—
生成物(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanoneHCID 5942455293%

反応手順

Starting from (7-chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone (139, scheme 26) and following the procedure described above for the synthesis of compound 6 (scheme 1, example 1), title compound 193 was obtained in (93% yield). LRMS (M+1) 387.4 (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772247B2
出典データセットuspto-grants-2010_08
ORD IDord-969e09178ae74772b882fc08d8db731e
出典メモuspto-grants-2010_08