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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353429생성일: 2026년 10월 25일

Triethylamine → 5-Amino-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/353429

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(2,6-Dichlorophenyl)hydrazine monohydrochlorideHCID 2723909—
반응물(1-Chloro-2-methylpropylidene)propanedinitrileHCID 23513711—
용매TetrahydrofuranHCID 8028—
생성물5-Amino-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole-4-carbonitrileHCID 2351371662.2%

반응 단계

A solution of (1-chloro-2-methylpropylidene)methane-1,1-dicarbonitrile (9.4 g, 61 mmol) in THF (250 mL) was treated with 2,6-dichlorophenylhydrazine hydrochloride (13.0 g, 61 mmol) followed by triethylamine (12.3 g, 122 mmol). The reaction was then heated to reilux for 18 h. The reaction was then cooled to room temp and partitioned between EtOAc (150 mL) and 1N NaOH (100 mL). The aqueous layer was extracted with EtOAc (2×150 mL) and the combined organic layers were washed with 10% aq. citric acid (150 mL), sat. aq. NaHCO3 (150 mL), and brine (150 mL). The organic layer was dried (MgSO4), filtered, and evaporated. The crude product was recrystallized from EtOAc/hexane to yield the desired pyrazole (11.2 g, 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06753329B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-75ffd4f0abad41cd87f7ac51ad6f9247
출처 메모uspto-grants-2004_06