ES2548386T3 - Formas cristalinas de saxagliptina - Google Patents

Formas cristalinas de saxagliptina Download PDF

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Publication number
ES2548386T3
ES2548386T3 ES10713211.0T ES10713211T ES2548386T3 ES 2548386 T3 ES2548386 T3 ES 2548386T3 ES 10713211 T ES10713211 T ES 10713211T ES 2548386 T3 ES2548386 T3 ES 2548386T3
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Spain
Prior art keywords
saxagliptin
crystalline forms
crystalline
water content
relative humidity
Prior art date
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ES10713211.0T
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English (en)
Inventor
Arthur Pichler
Josef Wieser
Christoph Langes
Milica Vukicevic
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Sandoz AG
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Sandoz AG
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Filing date
Publication date
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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Abstract

Formas cristalinas anhidras de monoclorhidrato de saxagliptina que tienen un contenido en agua de no más del 1,5% p/p.

Description

imagen1
imagen2
imagen3
imagen4
imagen5
imagen6
imagen7
imagen8
imagen9
E10713211
25-09-2015
Tabla 1: Ángulos 2-theta, valores de d e intensidades relativas de la forma I-S
Ángulo [º 2-Theta]
Valor de d [Angstrom] Int. rel [%]
6,72
13,145 100
10,30
8,591 4
11,68
7,577 3
13,52
6,548 12
14,63
6,054 46
15,15
5,846 36
16,60
5,340 32
17,91
4,952 53
18,80
4,721 7
19,19
4,624 7
20,33
4,368 4
21,46
4,141 4
22,17
4,010 5
24,50
3,634 17
27,01
3,301 6
28,16
3,169 12
29,78
3,001 9
30,59
2,922 9
31,33
2,855 9
31,87
2,808 3
34,27
2,616 4
36,25
2,478 5
La forma cristalina I-S de monoclorhidrato de saxagliptina obtenida anteriormente tiene un espectro de IR de reflectancia total atenuada con bandas de absorción a 2907, 2853, 1637, 1589, 1462, 1391, 1318, 1045, 1014 y 775 5 cm -1 (± 2 cm-1; figura 2)
Se sometió la forma cristalina I-S obtenida a análisis térmico diferencial. Tal como puede observarse en la figura 3 (curva inferior), la forma cristalina I-S no muestra endoterma de deshidratación significativa sino sólo un pico a 241ºC (Tcomienzo de 230ºC; velocidad de calentamiento de 10ºC/minuto, cápsula perforada). Se determinó el cloro iónico como del 10,7% (en teoría el 10,08%).
10 Se determinó el contenido en agua de la forma cristalina I-S obtenida como del 1,2% p/p usando un aparato de Karl
11
imagen10
imagen11
imagen12
E10713211
25-09-2015
Ángulo [º 2-Theta]
Valor de d [Angstrom] Int. rel. [%]
4,08
21,652 100
4,72
18,738 15
6,25
14,143 29
13,91
6,368 6
14,51
6,104 23
14,89
5,948 5
15,64
5,667 39
16,69
5,312 22
18,55
4,784 29
19,37
4,582 10
19,8
4,484 6
Se sometió la forma cristalina IV-S obtenida a análisis termogravimétrico. Tal como puede observarse en la figura 11, la forma cristalina IV-S muestra una pérdida de masa de aproximadamente el 12,8% desde el comienzo hasta 100ºC. Esta pérdida de masa corresponde a 2,86 moles de agua.
5 El análisis de sorción de humedad muestra un contenido en agua del 13,1% a una humedad relativa del 40% a 25ºC correspondiente a 2,94 moles de agua. El análisis de sorción de humedad muestra un contenido en agua del 12,8% correspondiente a una humedad relativa del 2,86% a una humedad relativa del 0%. El proceso es reversible.
A una humedad relativa de más del 40%, la forma IV-S se transforma de manera irreversible en la forma de dihidrato H2-1 conocida.
10
15

Claims (1)

  1. imagen1
    imagen2
ES10713211.0T 2009-04-09 2010-04-09 Formas cristalinas de saxagliptina Active ES2548386T3 (es)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US16791809P 2009-04-09 2009-04-09
EP09157723 2009-04-09
EP09157723 2009-04-09
US167918P 2009-04-09
EP09175259 2009-11-06
EP09175259 2009-11-06
PCT/EP2010/054692 WO2010115974A1 (en) 2009-04-09 2010-04-09 Crystal forms of saxagliptin

Publications (1)

Publication Number Publication Date
ES2548386T3 true ES2548386T3 (es) 2015-10-16

Family

ID=42935672

Family Applications (1)

Application Number Title Priority Date Filing Date
ES10713211.0T Active ES2548386T3 (es) 2009-04-09 2010-04-09 Formas cristalinas de saxagliptina

Country Status (12)

Country Link
US (2) US20120088808A1 (es)
EP (1) EP2417107B1 (es)
JP (2) JP6088245B2 (es)
KR (1) KR20120006047A (es)
CN (2) CN104016902B (es)
AU (1) AU2010233718B2 (es)
BR (1) BRPI1006547A2 (es)
CA (1) CA2757934C (es)
ES (1) ES2548386T3 (es)
PL (1) PL2417107T3 (es)
RU (1) RU2539590C2 (es)
WO (1) WO2010115974A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0487425A (ja) * 1990-07-31 1992-03-19 Fujitsu Ltd 回線切り替え装置
ES2548386T3 (es) * 2009-04-09 2015-10-16 Sandoz Ag Formas cristalinas de saxagliptina
ES2546866T3 (es) 2009-12-16 2015-09-29 Hetero Research Foundation Polimorfos de darunavir
CA2799762C (en) 2010-05-20 2018-03-06 Hetero Research Foundation Crystalline hydrochloride salt of darunavir
EP2608788A1 (en) 2010-10-04 2013-07-03 Assia Chemical Industries Ltd. Polymorphs of saxagliptin hydrochloride and processes for preparing them
WO2013036213A1 (en) 2011-09-07 2013-03-14 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dpp-iv inhibitor formulations
EP2578208B1 (en) 2011-10-06 2014-05-21 Sanovel Ilac Sanayi ve Ticaret A.S. DPP-IV inhibitor solid dosage formulations
WO2013136343A1 (en) 2012-03-12 2013-09-19 Mylan Laboratories Ltd. Amorphous saxagliptin hydrochloride
EP2841419A1 (en) * 2012-04-25 2015-03-04 Enantia, S.L. Crystalline forms of saxagliptin
AU2013264925B2 (en) 2012-05-24 2017-08-17 Apotex Inc. Salts of saxagliptin with organic acids
EP2867206A2 (en) 2012-07-02 2015-05-06 Ranbaxy Laboratories Limited Saxagliptin salts
WO2015067223A1 (en) 2013-11-06 2015-05-14 Zentiva, K., S. L-tartrate salt of (1s,3s,5s)-2-[(2s)-2-amino-2-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl) acetyl]-2-azabicyclo[3.1.0]hexane-3-carbonitrile and process for preparation thereof

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6032616B2 (ja) * 1976-08-24 1985-07-29 アレクサンダ− ガラツト 高い貯蔵安定性の無水アセチルサリチル酸ナトリウム
US6395767B2 (en) * 2000-03-10 2002-05-28 Bristol-Myers Squibb Company Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method
US7420079B2 (en) * 2002-12-09 2008-09-02 Bristol-Myers Squibb Company Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof
US6995183B2 (en) * 2003-08-01 2006-02-07 Bristol Myers Squibb Company Adamantylglycine-based inhibitors of dipeptidyl peptidase IV and methods
TWI354569B (en) * 2004-05-28 2011-12-21 Bristol Myers Squibb Co Coated tablet formulation and method
AU2005264065A1 (en) * 2004-07-16 2006-01-26 Warner-Lambert Company Llc Hair growth promoting agents
US20060035954A1 (en) * 2004-08-11 2006-02-16 Sharma Padam N Ammonolysis process for the preparation of intermediates for DPP IV inhibitors
PE20090696A1 (es) * 2007-04-20 2009-06-20 Bristol Myers Squibb Co Formas cristalinas de saxagliptina y procesos para preparar las mismas
ES2548386T3 (es) * 2009-04-09 2015-10-16 Sandoz Ag Formas cristalinas de saxagliptina

Also Published As

Publication number Publication date
RU2539590C2 (ru) 2015-01-20
CA2757934C (en) 2017-12-19
BRPI1006547A2 (pt) 2016-10-18
JP6088245B2 (ja) 2017-03-01
PL2417107T3 (pl) 2016-02-29
CN104016902A (zh) 2014-09-03
WO2010115974A1 (en) 2010-10-14
RU2011145054A (ru) 2013-05-20
US9260389B2 (en) 2016-02-16
US20120088808A1 (en) 2012-04-12
CN102459170B (zh) 2014-07-23
KR20120006047A (ko) 2012-01-17
AU2010233718B2 (en) 2015-11-05
EP2417107A1 (en) 2012-02-15
JP2016006063A (ja) 2016-01-14
CN102459170A (zh) 2012-05-16
AU2010233718A1 (en) 2011-10-27
JP2012523395A (ja) 2012-10-04
CN104016902B (zh) 2017-10-20
CA2757934A1 (en) 2010-10-14
EP2417107B1 (en) 2015-08-26
US20140200252A1 (en) 2014-07-17

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