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HRID 1695204作成日:2026年10月27日

Sodium Iodide → Way-361789

https://huagongshe.com/reaction/1695204

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DiisopropylethylamineHCID 81531—
反応物5-Bromovaleryl chlorideHCID 521173—
反応物3-Amino-5-(4-methoxyphenyl)pyrazoleHCID 2756469—
反応物N-AcetylhomopiperazineHCID 4186202—
溶媒DimethylformamideHCID 6228—
生成物Way-361789HCID 2486058299.4%

反応条件

温度-5 °C

反応手順

To a solution of 5-(4-methoxyphenyl)-1H-pyrazol-3-ylamine (12 g, 62.8 mmol) and N,N-diisopropylethylamine (10.96 mL, 62.8 mmol) in dry N,N-dimethylformamide (150 mL) at −10° C. was added a solution of 5-bromovaleryl chloride (8.4 mL, 62.8 mmol) in dry N,N-dimethylformamide (50 mL) slowly (˜40 min) and the reaction mixture was allowed to stir at −10 to 0° C. for 8 hrs. Sodium iodide (9.44 g, 62.8 mmol) was added at 0° C. and followed by N-acetylhomopiperazine (8.24 mL, 62.8 mmol) and N,N-diisopropylethylamine (10.96 mL, 62.8 mmol) and the reaction mixture was allowed to stir at 50° C. for 18 hrs. The solvent was removed in vacuo. The residue was dissolved in methylene chloride (500 mL) and saturated aqueous sodium bicarbonate (500 mL) and the mixture was stirred at room temperature for 30 minutes. The organic layer was separated, dried over sodium sulfate, and the solvent was removed in vacuo to provide 25.8 g (99%) of 5-(4-acetyl-1,4-diazepan-1-yl)-N-(5-(4-methoxyphenyl)-1H-pyrazol-3-yl)pentanamide as a thick light yellow oil (crude).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163729B2
出典データセットuspto-grants-2012_04
ORD IDord-4c097c81e0d94457b203229c0c442b8b
出典メモuspto-grants-2012_04