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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527318생성일: 2026년 10월 26일

Hydrazine hydrate (1:1) → 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/527318

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물2-Cyano-3,3-bis(methylthio)acrylamideHCID 2747746—
반응물4-(4-Methyl-1h-imidazol-1-yl)benzenamineHCID 16005170—
용매EthanolHCID 702—
생성물5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamideHCID 86701914—

반응 조건

온도75 °C

반응 단계

Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4-methyl-1-(4-aminophenyl)-1H-imidazole (1.0 eq.). Stirred reaction at 75° C. until starting amide was absent by HPLC. Once complete (18 hrs), reaction was brought to room temperature and filtered to obtain a light yellow powder as product. Product was allowed to dry under vacuum for 1 hr. Product was then suspended in 10 mL EtOH and hydrazine hydrate (1 eq.) was added dropwise. Reaction was heated at 75° C. until intermediate was absent (HPLC). Once intermediate was absent (18 hrs), reaction was brought to room temperature and filtered to obtain 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide as a yellow powder. Product was allowed to dry under vacuum for 1 hr.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346792B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-ad016818b21d49a28565f11af43437cf
출처 메모uspto-grants-2016_05