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HRID 522082作成日:2026年10月26日

Diisopropylethylamine → HCID 178434562、化合物

https://huagongshe.com/reaction/522082

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物5-(2,4-dichloro-5-(pyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acidHCID 118497035—
反応物HCID 178434557HCID 178434557—
反応物HCID 178484293HCID 178484293—
溶媒DimethylformamideHCID 6228—
生成物HCID 178434562HCID 17843456269.4%

反応手順

To a solution of 5-(2,4-dichloro-5-(pyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acid (Example 111, 210 mg, 0.46 mmol), 3-methyl-1H-pyrazol-4-amine (68 mg, 0.69 mmol) and DIPEA (0.32 mL, 1.85 mmol) in anhydrous DMF (4 mL) was added 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (264 mg, 0.69 mmol). The reaction was stirred at room temperature for 1 hour under nitrogen. The reaction was partitioned between EtOAc (20 mL) and water (20 mL). The organic layer was collected, washed with brine (15 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by elution through an SCX-2 column using MeOH followed by 7N ammonia in MeOH, followed by purification using silica gel column chromatography eluting with EtOAc followed by 10% MeOH in DCM to afford the title compound (170 mg, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328096B2
出典データセットuspto-grants-2016_05
ORD IDord-c553713fe9f2471fab68a2f3750d1598
出典メモuspto-grants-2016_05