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ChemicalBook CAS DataBase List Apixaban Impurity 22
1449510-64-8

Apixaban Impurity 22 synthesis

9synthesis methods
1575-61-7 Synthesis
5-Chlorovaleryl chloride

1575-61-7
375 suppliers
$14.00/1g

1423803-24-0 Synthesis
Apixaban Impurity 17

1423803-24-0
55 suppliers
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Apixaban Impurity 22

1449510-64-8
33 suppliers
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-

Yield:1449510-64-8 5.1 g

Reaction Conditions:

with triethylamine in tetrahydrofuran at 60 - 65; for 4 h;

Steps:

9 Preparation of compound (IIB)

In 250 mL 3-neck round bottom flask equipped with mechanical stirrer, thermometer and addition funnel, compound (III) (10 g), 5-chlorovalaroyl chloride (10.27 g), triethylamine (9.4 g) and THF (70 mL) were heated at 60°C to 65°C for 4 hours. The reaction mixture was cooled at 25°C to 35°C and water (200 mL) was added. The reaction mixture was distilled to remove THF and cooled to 25°C to 35°C. The reaction mixture was stirred for 1 hour and filtered. The wet-cake was washed with water and dried to obtain 5.1 g of compound (IIB). The compound (IIB) was characterized by X-ray powder diffraction pattern (FIG.17). The solid compound was recrystallized in ethyl acetate at 65°C to obtain pure compound (IIB)

References:

WO2014/203275,2014,A2 Location in patent:Page/Page column 39

503615-03-0 Synthesis
3-Morpholino-1-(4-nitrophenyl)-5,6-dihydropyridin-2(1H)-one

503615-03-0
353 suppliers
$31.00/1g

Apixaban Impurity 22

1449510-64-8
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Apixaban Impurity 22 Related Search:

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