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HRID 875783作成日:2026年10月26日

Triethylamine → N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/875783

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
反応物1-[(4-methoxyphenyl)methyl]-1H-pyrazole-4-carboxylic acidHCID 43565362—
反応物5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amineHCID 60205276—
溶媒DichloromethaneHCID 6344—
生成物N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxamideHCID 6020547639.8%

反応手順

A mixture of 5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (300 mg, 1.30 mmol, Example 1, Step H), 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylic acid (636 mg, 2.74 mmol), BOP-Cl (697 mg, 2.74 mmol), and triethylamine (0.909 mL, 6.52 mmol) in DCM (5 mL) was processed as described in Example 62, Step A, to provide N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxamide (230 mg, 39% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08981085B2
出典データセットuspto-grants-2015_03
ORD IDord-97608d6f8ee64417b5ecad63dd3db4f0
出典メモuspto-grants-2015_03