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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244717Erstellt: 26. Oktober 2026

5-methyl-1H-pyrazole-3-carboxylic acid → N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-5-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/244717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-methyl-1H-pyrazole-3-carboxylic acidHCID 9822—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt6-(1H-Indol-4-yl)-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-amineHCID 58267995—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDiisopropylethylamineHCID 81531—
ProduktN-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-5-methyl-1H-pyrazole-3-carboxamideHCID 44540242—

Reaktionsschritte

5-Methyl-1H-pyrazole-3-carboxylic acid (10 mg) in DMF (0.2 ml) was treated with N-[(dimethylamino)(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yloxy)methylidene]-N-methylmethanaminium hexafluorophosphate (27 mg) in DMF (0.2 ml) and DIPEA (0.03 ml). The reaction mixture was shaken for five min prior to treatment with 6-(1H-indol-4-yl)-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-amine (20 mg) in DMF (0.2 ml). The reaction mixture was shaken for five min and left to stand at 22° C. for 18 h. The solvent was removed in vacuo and the product re-dissolved in methanol (1 ml) prior to application on to an SCX SPE cartridge (1 g). The product was eluted after 1 h with 2M ammonia in methanol (2×3 ml), the fractions were combined and concentrated under a stream of nitrogen using blow down apparatus. Purification by mass directed preparative HPLC (Method C) afforded the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658635B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-222ac297bb7d4c768557abf89a2cb8ca
Quellennotizuspto-grants-2014_02