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HRID 1874497Erstellt: 24. Oktober 2026

Tetrahydrofuran → N-[5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-2-methylphenyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide

https://huagongshe.com/de/reaction/1874497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktThionyl ChlorideHCID 24386—
EduktDimethyl-1,3-oxazole-5-carboxylic acidHCID 1132979—
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]-2,4-dimethyl-1,3-oxazole-5-carboxamideHCID 5774940264,3%

Reaktionsschritte

In the same manner as in Example 55 and using 2,4-dimethyl-1,3-oxazole-5-carboxylic acid (56.6 mg, 0.401 mmol), tetrahydrofuran (5 mL), thionyl chloride (69.1 μL, 0.796 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-methylphenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (117 mg, 0.362 mmol) and N,N-dimethylacetamide (6 mL) as starting materials, the title compound (104 mg, 64%) was obtained as a pale-brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304557B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-86f0800f8f98406cb5fbb2cf96c7724e
Quellennotizuspto-grants-2012_11