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HRID 75606作成日:2026年10月24日

3-Bromophenylhydrazine hydrochloride → 1-(3-Bromophenyl)-3-tert-butyl-1H-pyrazol-5-amine

https://huagongshe.com/ja/reaction/75606

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromophenylhydrazine hydrochlorideHCID 33757—
反応物Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
溶媒EthanolHCID 702—
生成物1-(3-Bromophenyl)-3-tert-butyl-1H-pyrazol-5-amineHCID 1844987854%

反応手順

A mixture of 3-bromophenylhydrazine hydrochloride (5.00 g, 22.4 mmol) and 4,4-dimethyl-3-oxo-pentanenitrile (4.29 g, 33.6 mmol) in absolute ethanol (55 mL) was stirred at reflux for 18 h and cooled, then concentrated in vacuo. The residue was suspended in sat. aq. NaHCO3 (50 mL) and extracted with EtOAc (3×50 mL). The combined organics were dried (Na2SO4) and concentrated in vacuo. The residue was purified by FCC, using 0-5% [2M NH3 in MeOH] in DCM, to give the title compound (3.56 g, 54%). LCMS (Method 1): Rt 3.33 min, m/z 294, 296 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835431B2
出典データセットuspto-grants-2014_09
ORD IDord-c70ba990100341a893ddcfbb212b4c89
出典メモuspto-grants-2014_09