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HRID 618804作成日:2026年10月25日

1-Methyl-4-nitro-3-propyl-1H-pyrazole-5-carboxamide → 4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/618804

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methyl-4-nitro-3-propyl-1H-pyrazole-5-carboxamideHCID 2754492—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamideHCID 3338044—

反応手順

A stirred suspension of 1-methyl4-nitro-3-n-propylpyrazole-5-carboxamide (EP-A-0463756; 237.7 g, 1.12 mol) and 5% palladium on charcoal (47.5 g) in ethyl acetate (2.02 l) was hydrogenated at 344.7 kPa (50 psi) and 50° C. for 4 hours, when the uptake of hydrogen was complete. The cool reaction mixture was filtered, then the filter pad washed with ethyl acetate, the combined filtrate and washings thus furnishing an ethyl acetate solution of the title compound (EP-A-0463756) which was of sufficient purity to use directly in the next stage of the reaction sequence (see Preparation 4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05955611
出典データセットuspto-grants-1999_09
ORD IDord-2c5b9173c24a489b801f00bda7fd8540
出典メモuspto-grants-1999_09