WO2023181076 - PROCESS FOR PREPARATION OF PURE SITAGLIPTIN AND SALTS THEREOF

National phase entry is expected:
Publication Number WO/2023/181076
Publication Date 28.09.2023
International Application No. PCT/IN2023/050283
International Filing Date 24.03.2023
Title **
[English] PROCESS FOR PREPARATION OF PURE SITAGLIPTIN AND SALTS THEREOF
[French] PROCÉDÉ DE PRÉPARATION DE SITAGLIPTINE PURE ET DE SES SELS
Applicants **
DR. REDDY'S LABORATORIES LIMITED House No. 8-2-337 Street Road No. 3, Banjara Hills Hyderabad, Telangana 500034, IN
Inventors
KURELLA, Srinivas House No. 2-66/5, Plot No.5, Gajularamaram, Qutubullapur, Hyderabad, Telangana. Hyderabad 500055, IN
PANUGANTI, Ranjeeth House No. 16-117/596, Plot No. 596, Alwyn colony, Patancheru, Hyderabad, Telangana. Hyderabad 502319, IN
Priority Data
202241016929   25.03.2022   IN
Application details
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International Searching Authority
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Entry into National Phase under
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Quotation for National Phase entry

Country StagesTotal
China Filing1512
EPO Filing, Examination11420
Japan Filing594
South Korea Filing575
USA Filing, Examination13035
MasterCard Visa

Total: 27136

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] The present application relates to substantially pure Sitagliptin and its pharmaceutically acceptable salts, and more particularly a process for preparing substantially pure Sitagliptin and its pharmaceutically acceptable salts and pharmaceutical compositions thereof. The present application also describes pharmaceutical compositions comprising sitagliptin or a salt thereof having less than about 100 ppm of compound of formula VII and/or less than about 1 ppm of Nitrosamine impurity of the compound of formula VIII.[French] La présente demande concerne de la sitagliptine sensiblement pure et ses sels pharmaceutiquement acceptables, et plus particulièrement un procédé de préparation de sitagliptine sensiblement pure et de ses sels pharmaceutiquement acceptables et des compositions pharmaceutiques associées. La présente demande concerne également des compositions pharmaceutiques comprenant de la sitagliptine ou un sel de celle-ci ayant moins d'environ 100 ppm de composé de formule VII et/ou moins d'environ 1 ppm d'impureté nitrosamine du composé de formule VIII.
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