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HRID 1035456作成日:2026年10月25日

3-tert-butyl-1-phenyl-1H-pyrazol-5-amine → HCID 44133720、化合物

https://huagongshe.com/reaction/1035456

反応式

関与物質

役割名称HCID仕込み量
反応物3-tert-butyl-1-phenyl-1H-pyrazol-5-amineHCID 770634—
反応物TrimethylaluminumHCID 16682925—
反応物Methyl 3-(3-oxo-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)benzoateHCID 44134094—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 44133720HCID 44133720—

反応手順

Method H1: A solution of AlMe3 (solution in toluene 2M, 0.85 mL, 1.68 mmol,) was added dropwise to a cooled (0 C) solution of 3-tert-butyl-1-phenyl-1H-pyrazol-5-amine (362 mg, 1.68 mmol) in THF (5.0 mL). When the addition was complete, the mixture was allowed to warm to room temperature and stirring was continued for 30 minutes. Then methyl 3-(3-oxo-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)benzoate (100 mg, 0.336 mmol) was added and the mixture was heated under reflux for 19 h. The mixture was cooled to room temperature and carefully quenched with 5% aq HCl (3.0 mL). After evaporation of solvent, the residue was retaken in CH2Cl2, washed with saturated solution of NaHCO3 and dried over MgSO4 and evaporated under vacuum. The obtained residue was chromatographied (eluent: CH2Cl2/EtOAc: 2/1 towards 1/3) and the title compound was obtained as a slightly yellow solid (29 mg, 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546387B2
出典データセットuspto-grants-2013_10
ORD IDord-66eafb60a0a346a695bd788c9242f3ad
出典メモuspto-grants-2013_10