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1028634-76-5

Atazanavir Impurity 8 synthesis

1synthesis methods
methyl N-(1-{[4-(2-{[(benzyloxy)carbonyl]amino}-3,3-dimethyl-N'-{[4-(pyridin-2-yl)phenyl]methyl}butanehydrazido)-3-hydroxy-1-phenylbutan-2-yl]carbamoyl}-2,2-dimethylpropyl)carbamate

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Atazanavir Impurity 8

1028634-76-5
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Yield:-

Reaction Conditions:

with ammonium formate;5%-palladium/activated carbon in methanol at 40; for 2 h;

Steps:

5

Example 5 - Preparation of compound (8); Compound 7 (12.2 g), obtained as described in example 4, was suspended in methanol (90 mL), then added with 1.33 g of Pd-C 5% and the suspension was heated to reflux. The mixture was then cooled to 40°C, and a solution of 4.93 g of ammonium formate in methanol/water was added over about one hour. The reaction was heated at 40°C for about one hour, then cooled to about 25-30°C. The suspension was filtered and the filtrate was evaporated in vacuo to a solid residue, which was added with 100 mL of EtOAc and washed with a 5% aqueous solution of NaHCO3. The organic phase was dried over anhydrous sodium sulphate, filtered, and evaporated in vacuo to yield 9.47 of compound 8 as a white solid, which was used for the next step without further purification.

References:

EP1930324,2008,A1 Location in patent:Page/Page column 7

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