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HRID 40149作成日:2026年10月23日

2-Pyrrolidone → 1-Benzyl-N-(3,4-difluorobenzyl)-6-(3,4-dihydro-2H-pyrrol-5-ylamino)-5-fluoro-2-isopropyl-1H-indole-3-carboxamide

https://huagongshe.com/ja/reaction/40149

反応式

関与物質

役割名称HCID仕込み量
反応物2-PyrrolidoneHCID 12025—
反応物Phosphorus oxychlorideHCID 24813—
反応物6-amino-1-benzyl-N-(3,4-difluorobenzyl)-5-fluoro-2-isopropyl-1H-indole-3-carboxamideHCID 59762400—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物1-Benzyl-N-(3,4-difluorobenzyl)-6-(3,4-dihydro-2H-pyrrol-5-ylamino)-5-fluoro-2-isopropyl-1H-indole-3-carboxamideHCID 59762436—

反応条件

温度110 °C

反応手順

A mixture of 2-pyrrolidinone (47 mg, 0.55 mmol) and POCl3 (0.10 ml, 1.1 mmol) was stirred at 0° C. to room temperature for 2h. To the above mixture was then added a solution of 6-amino-1-benzyl-N-(3,4-difluorobenzyl)-5-fluoro-2-isopropyl-1H-indole-3-carboxamide (Compound 172, 50 mg, 0.11 mmol) in toluene (3 ml). The reaction was heated to 110° C. for 16 h and was cooled to room temperature, diluted with EtOAc, washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by reverse phase chromatography on C18 bonded silica gel (MeOH) to yield the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524917B2
出典データセットuspto-grants-2013_09
ORD IDord-87efb787dd884b16baaff4567165b540
出典メモuspto-grants-2013_09