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HRID 251342作成日:2026年10月27日

Sodium Hydroxide → 3-[5-amino-4-(4-methyl-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide

https://huagongshe.com/reaction/251342

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium AcetateHCID 517045—
反応物Aminomalononitrile p-toluenesulphonateHCID 563049—
反応物3-amino-N-cyclopropyl-4-methylbenzamideHCID 11983854—
溶媒WaterHCID 962—
溶媒Ethyl orthoformateHCID 31214—
生成物3-[5-amino-4-(4-methyl-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamideHCID 1116470330%

反応条件

温度120 °C

反応手順

A mixture of 3-amino-N-cyclopropyl-4-methyl-benzamide 1 (380 mg, 2.0 mmol) in 2.0 mL of triethyl orthoformate was stirred at 120° C. in microwave for 20 minutes. The solvent was removed under reduced pressure. The residue was dissolved in 5 mL of acetic acid and then was added aminomalononitrile p-toluenesulfonate (506 mg, 2.0 mmol) and sodium acetate (164 mg, 2.0 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was diluted with 20 mL of water and then its pH was adjusted to 8.0 by aqueous NaOH. The resulting mixture was extracted with EtOAc (3×50 mL). The combined organic layers were washed with water (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated in vacuo evaporated. The residue was purified by silica gel column chromatography (10/1, methylene chloride:methanol) to give 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide 3 as a colorless solid (170 mg, 30%). HPLC (4 minute gradient) tR=1.39 min; MS m/z 282 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863314B2
出典データセットuspto-grants-2011_01
ORD IDord-58d9bc116e3d41c3b7a02aebc0b2eda8
出典メモuspto-grants-2011_01