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HRID 31379作成日:2026年10月24日
2-(Ethoxymethylene)propanedinitrile → 5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrile
https://huagongshe.com/ja/reaction/31379
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| 反応物 | [2-Fluoro-4-(methylsulfonyl)phenyl]hydrazine | HCID 2782739 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrile | HCID 21897593 | — |
反応手順
To a stirred suspension of 2-fluoro-4-methylsulfonylphenyl hydrazine (1) (4.0336 Kg; 1 eq) (commercially available from, e.g., Peakdale Molecular, Ltd.) in methanol (12.7723 Kg) was added a suspension of ethoxymethylene malononitrile (2.6564 Kg, 1.101 equivalents) in methanol (11.212 Kg) at a rate sufficiently slow to maintain the reaction mixture at −10° to 0° C. with reactor jacket cooling. After the addition had been completed, the reaction mixture was stirred for 1 hour at −6° C. and then heated to reflux for 5 hours, at which time the reaction mixture gave a pyrazole (3): hydrazine (1) HPLC peak area ratio of 105:1. Solvent (20.5153 Kg) was then distilled off the reaction mixture at atmospheric pressure, leaving a residue having less than 20% of the original volume. The resulting mixture was used directly in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07425630B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-2cf28deae1a344dd9efb094b5ca7a968 |
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| 出典メモ | uspto-grants-2008_09 |
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