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HRID 250552作成日:2026年10月26日

1H-Pyrrolo(2,3-b)pyridine → Propane-1-sulfonic acid [3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluoro-phenyl]-amide

https://huagongshe.com/reaction/250552

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Pyrrolo(2,3-b)pyridineHCID 9222—
反応物5-bromo-1H-indazoleHCID 761929—
反応物5-Fluoro-1H-pyrrolo[2,3-b]pyridineHCID 20784462—
反応物5-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 24229213—
反応物propane-1-sulfonic acid [2-fluoro-3-(5-fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-phenyl]-amideHCID 58087704—
反応物propane-1-sulfonic acid [2-fluoro-3-(1H-pyrrolo[2,3-b]pyridin-3-carbonyl)-phenyl]-amideHCID 58087847—
生成物Propane-1-sulfonic acid [3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluoro-phenyl]-amideHCID 58086733—

反応手順

Using the protocol of Scheme 14, substituting 5-bromo-azaindole with either 5-chloro-7-azaindole (80, prepared as described in Example 9), 5-fluoro-7-azaindole (81, prepared as described in Example 9) or 7-azaindole in Step 6, propane-1-sulfonic acid [3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluoro-phenyl]-amide P-1013 (MS (ESI) [M−H+]−=394.1), propane-1-sulfonic acid [2-fluoro-3-(5-fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-phenyl]-amide P-1028 (MS (ESI) [M−H+]−=378.1), and propane-1-sulfonic acid [2-fluoro-3-(1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-phenyl]-amide P-1056 (MS (ESI) [M+H+]+=362.2) were prepared, respectively;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863288B2
出典データセットuspto-grants-2011_01
ORD IDord-0292e2944f1e4bd786619c33751fa9a7
出典メモuspto-grants-2011_01