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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 544198생성일: 2026년 10월 27일

(2,4,6-Trichlorophenyl)hydrazine → 5-Cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedione

https://huagongshe.com/reaction/544198

반응식

참여 물질

역할이름HCID투입량
반응물(2,4,6-Trichlorophenyl)hydrazineHCID 79234—
반응물alpha-cyano-beta-methyl-beta-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamideHCID 70513266—
생성물5-Cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedioneHCID 13232255—

반응 단계

Following the method of Example 1, N-ethoxycarbonylcyanoacetamide is heated with triethyl orthoacetate and acetic anhydride to give α-cyano-β-ethoxy-β-methyl-N-ethoxycarbonylacrylamide, which in turn is reacted with 2,4,6-trichlorophenylhydrazine. The resulting compound α-cyano-β-methyl-β-(2,4,6-trichlorophenylhydrazino)-N-ethoxycarbonylacrylamide (m.p.=183°-184°) is cyclized, yielding 5-cyano-6-methyl-1-(2,4,6-trichloroanilino)-2,4-pyrimidinedione, m.p.=>305°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04448961
출처 데이터셋uspto-grants-1984_05
ORD IDord-8e0b1715df694670bb8bf8aa71e38e72
출처 메모uspto-grants-1984_05