Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31379생성일: 2026년 10월 23일
2-(Ethoxymethylene)propanedinitrile → 5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrile
https://huagongshe.com/ko/reaction/31379
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| 반응물 | [2-Fluoro-4-(methylsulfonyl)phenyl]hydrazine | HCID 2782739 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrile | HCID 21897593 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425630B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-2cf28deae1a344dd9efb094b5ca7a968 |
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| 출처 메모 | uspto-grants-2008_09 |
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