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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 522082Erstellt: 24. Oktober 2026

Diisopropylethylamine → HCID 178434562, Verbindung

https://huagongshe.com/de/reaction/522082

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt5-(2,4-dichloro-5-(pyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acidHCID 118497035—
EduktHCID 178434557HCID 178434557—
EduktHCID 178484293HCID 178484293—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178434562HCID 17843456269,4%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328096B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-c553713fe9f2471fab68a2f3750d1598
Quellennotizuspto-grants-2016_05