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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061545생성일: 2026년 10월 27일

3-ethyl-1H-pyrazol-5-amine → 4-(2,4-Dichlorophenyl)-7-ethyl-2-methyl-pyrazolo[1,5-a]-1,3,5-triazine

https://huagongshe.com/reaction/1061545

반응식

참여 물질

역할이름HCID투입량
반응물3-ethyl-1H-pyrazol-5-amineHCID 21991095—
반응물N-(1-(methylthio)ethylidene)-2,4-dichlorobenzamideHCID 22184679—
용매1,4-DioxaneHCID 31275—
생성물4-(2,4-Dichlorophenyl)-7-ethyl-2-methyl-pyrazolo[1,5-a]-1,3,5-triazineHCID 2218468914%

반응 단계

A mixture of 3-amino-5-ethylpyrazole (10.3 g, 39.3 mmol) and N-(1-(methylthio)ethylidene)-2,4-dichloro-benzamide (4.0 g, 35.7 mmol) in anhydrous dioxan (20 mL) was stirred at reflux temperature under a nitrogen atmosphere for 16 h. After being cooled to ambient temperature, the reaction mix was concentrated in vacuo and the residue was treated with dichloromethane. The resulting supsension was filtered and the filtrate was concentrated in vacuo to afford an oil (1.5 g, 14% yield): NMR (CDCl3,300 MHz): δ 7.62 (d, 1H, J=8), 7.59 (d, 1H, J=2), 7.45 (dd, 1H, J=8,2), 6.42 (s, 1H), 2.82 (q, 2H, J=8), 2.73 (s, 3H), 1.30 (t, 3H, J=8).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960583B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-3550ee809b1546f6b72375e364609e96
출처 메모uspto-grants-2005_11