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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1607231생성일: 2026년 10월 25일

Triethylamine → N-(3,5-dimethylisoxazol-4-yl)-3-(4-chlorophenyl)-4-carbomethoxy-4-methyl-4,5-dihydro-1H-pyrazole-1-carboxamide

https://huagongshe.com/reaction/1607231

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,5-Dimethylisoxazole-4-isocyanateHCID 2736266—
반응물3-(4-chlorophenyl)-4-carbomethoxy-4-methyl-4,5-dihydro-1H-pyrazole hydrochlorideHCID 19852122—
용매DichloromethaneHCID 6344—
생성물N-(3,5-dimethylisoxazol-4-yl)-3-(4-chlorophenyl)-4-carbomethoxy-4-methyl-4,5-dihydro-1H-pyrazole-1-carboxamideHCID 1985278595%

반응 단계

3-(4-chlorophenyl)-4-carbomethoxy-4-methyl-4,5-dihydro-1H-pyrazole hydrochloride (10 mmole), triethylamine (20 mmole), methylene chloride (30 ml and 3,5-dimethylisoxazole-4-yl isocyanate (Maybridge Chemical Co. Ltd.) (10 mmole) were reacted by stirring at room temperature for 30 minutes. The reaction mixture was then washed twice with water, dried with magnesium sulfate concentrated giving a 95% yield of N-(3,5-dimethylisoxazol-4-yl)-3-(4-chlorophenyl)-4-carbomethoxy-4-methyl-4,5-dihydro-1H-pyrazole-1-carboxamide mp 214°-216° C. NMR data was consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04863947
출처 데이터셋uspto-grants-1989_09
ORD IDord-163a787293e64610890665b1deaaa9f7
출처 메모uspto-grants-1989_09