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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874463Erstellt: 26. Oktober 2026

Tetrahydrofuran → N-[5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktThionyl ChlorideHCID 24386—
Edukt1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
EduktN-[6-(3-amino-4-methylphenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749401—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-[5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamideHCID 5774928947%

Reaktionsschritte

In the same manner as in Example 55 and using 1-methyl-1H-pyrazole-5-carboxylic acid (86.0 mg, 0.686 mmol), tetrahydrofuran (5 mL), thionyl chloride (118 μL, 1.36 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-methylphenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (200 mg, 0.619 mmol) and N,N-dimethylacetamide (6 mL) as starting materials, the title compound (125 mg, 47%) was obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304557B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-8d59a6b06a25475ba5a142d1c09ad1d1
Quellennotizuspto-grants-2012_11