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HRID 2406114作成日:2026年10月27日

Ammonia → 5-amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/2406114

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrogen PeroxideHCID 784—
反応物5-Amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carbonitrileHCID 12150554—
溶媒EthanolHCID 702—
溶媒DichloromethaneHCID 6344—
生成物5-amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carboxamideHCID 12150561—

反応手順

2 g (9.4 mmol) of 5-amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carbonitrile (Example 1A) are dissolved in 25 ml of ethanol, and a mixture of 20 ml of 30% strength hydrogen peroxide and 40 ml of 25% strength ammonia is added. The solution is stirred at room temperature overnight and then concentrated to about 15 ml in a rotary evaporator. The oily emulsion resulting thereby is taken up in dichloromethane. It is washed several times with water and saturated sodium thiosulphate solution. Drying over magnesium sulphate is followed by removal of the solvent in vacuo. The residue is purified by preparative HPLC (YMC Gel ODS-AQ S 5/15 μm; eluent A: water, eluent B: acetonitrile; gradient: 0 min 30% B, 5 min 30% B, 50 min 95% B). 0.88 g (40% of theory) of the product is obtained as colourless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08809348B2
出典データセットuspto-grants-2014_08
ORD IDord-b70d72d0679b414e8e11547f6923af31
出典メモuspto-grants-2014_08