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HRID 353429作成日:2026年10月26日

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

https://huagongshe.com/reaction/353429

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(2,6-Dichlorophenyl)hydrazine monohydrochlorideHCID 2723909—
反応物(1-Chloro-2-methylpropylidene)propanedinitrileHCID 23513711—
溶媒TetrahydrofuranHCID 8028—
生成物5-Amino-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole-4-carbonitrileHCID 2351371662.2%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06753329B2
出典データセットuspto-grants-2004_06
ORD IDord-75ffd4f0abad41cd87f7ac51ad6f9247
出典メモuspto-grants-2004_06