IP Library Patent Application 11546303
Patent Application
App. No. 11/546,303

Stable polymorph of flibanserin

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Quick Facts
Patent No.
US None
App. No.
11/546,303
Abstract

The invention relates to the polymorph A of flibanserin, to a technical process for the preparation thereof, as well as to the use thereof for preparing medicaments.

Claims (610)

1 ) A crystalline polymorph, designated form A, of flibanserin 1,

having an endothermic maximum at about 161 ° C. which occurs during thermal analysis using DSC.

2 ) Flibanserin 1 comprising form A according to claim 1 .

3 ) A process for preparing form A of flibanserin 1 according to claim 1 ,

said process comprising:

(a) reacting a benzimidazolone 2

wherein R denotes a suitable amino protecting group,

with a piperazine 3

wherein X is a leaving group selected from chlorine, bromine, iodine, methanesulphonate, trifluoromethanesulphonate and para-toluenesulphonate, in a suitable solvent selected from water, alcohols, mixtures of water with alcohols, polar aprotic solvents and mixtures of polar aprotic solvents with water, in the presence of a suitable base, and

(b) cleaving the amino protecting group R under suitable cleaving conditions.

4 ) A process according to claim 3 , wherein the reaction of 2 with 3 is conducted at a temperature of at least 50° C.

5 ) A process according to claim 4 , wherein heating is conducted for about 10 minutes to about 12 hours.

6 ) A process for preparing flibanserin 1 according to claim 2 ,

said process comprsing:

(a) reacting a benzimidazolone 2

wherein R denotes a suitable amino protecting group,

with a piperazine 3

wherein X is a leaving group selected from chlorine, bromine, iodine, methanesulphonate, trifluoromethanesulphonate and para-toluenesulphonate, in a suitable solvent selected from water, alcohols, mixtures of water with alcohols, polar aprotic solvents and mixtures of polar aprotic solvents with water, in the presence of a suitable base, and

(b) cleaving the amino protecting group R under suitable cleaving conditions.

7 ) A process according to claim 6 , wherein the reaction of 2 with 3 is conducted at a temperature of at least 50° C.

8 ) A process according to claim 7 , wherein heating is conducted for about 10 minutes to about 12 hours.

9 ) Form A of flibanserin 1 obtained by the process according to claim 3 .

10 ) Filbanserin 1 obtained by the process according to claim 6 .

11 ) A polymorph of flibanserin 1 characterized by the following X-ray powder diffraction pattern:

d-

d-

Peak

Peak

Back.

Rel.

Angle

value

value

width

int

int

int

[°2Θ]

α1 [Å]

α2 [Å]

[°2Θ]

[counts]

[counts]

[%]

Signif.

5.195

16.9967

17.0390

0.960

8

69

0.1

1.05

9.045

9.7689

9.7931

0.100

92

96

1.3

0.97

9.335

9.4660

9.4896

0.080

114

98

1.6

0.88

10.025

8.8160

8.8379

0.140

400

100

5.5

7.18

10.595

8.3430

8.3637

0.140

204

102

2.8

3.46

11.290

7.8309

7.8503

0.140

467

104

6.4

6.91

13.225

6.6891

6.7058

0.180

548

112

7.5

13.10

14.595

6.0642

6.0793

0.180

404

121

5.5

9.17

15.460

5.7268

5.7410

0.140

4186

125

57.3

23.20

16.655

5.3185

5.3317

0.200

515

130

7.0

12.38

17.085

5.1856

5.1985

0.100

1347

132

18.4

2.78

17.285

5.1260

5.1388

0.060

1399

135

19.1

2.26

17.420

5.0866

5.0992

0.100

1204

135

16.5

4.71

18.140

4.8863

4.8984

0.180

1043

139

14.3

13.14

18.650

4.7538

4.7656

0.120

1063

142

14.5

0.91

19.140

4.6332

4.6447

0.140

7310

144

100.0

32.77

19.820

4.4757

4.4869

0.160

3624

146

49.6

9.02

20.080

4.4184

4.4294

0.140

5402

149

73.9

21.06

20.385

4.3530

4.3638

0.160

2652

149

36.3

23.25

21.215

4.1845

4.1949

0.160

369

154

5.0

5.78

21.890

4.0570

4.0670

0.200

773

156

10.6

3.09

22.630

3.9259

3.9357

0.280

4277

161

58.5

74.66

23.210

3.8291

3.8386

0.120

484

164

6.6

3.33

24.355

3.6516

3.6607

0.060

2725

169

37.3

1.16

24.610

3.6144

3.6234

0.140

3540

172

48.4

17.08

24.995

3.5596

3.5684

0.100

529

174

7.2

1.01

25.260

3.5228

3.5316

0.120

557

174

7.6

3.02

26.575

3.3514

3.3597

0.240

2421

182

33.1

42.58

27.155

3.2811

3.2893

0.140

676

185

9.2

1.32

27.310

3.2629

3.2710

0.100

767

185

10.5

2.75

27.865

3.1991

3.2071

0.120

420

188

5.7

1.08

28.210

3.1608

3.1686

0.100

1467

190

20.1

0.79

28.325

3.1482

3.1560

0.140

1789

190

24.5

4.41

28.650

3.1132

3.1210

0.180

1204

190

16.5

11.65

29.520

3.0234

3.0309

0.220

1011

196

13.8

15.74

30.250

2.9521

2.9594

0.120

159

199

2.2

1.22

31.105

2.8729

2.8800

0.360

282

204

3.9

8.14

31.905

2.8026

2.8096

0.100

339

207

4.6

0.96

32.350

2.7651

2.7720

0.120

237

210

3.2

3.01

33.300

2.6884

2.6950

0.180

1347

216

18.4

14.06

33.640

2.6620

2.6686

0.100

404

216

5.5

1.45

34.880

2.5701

2.5765

0.200

202

222

2.8

1.04

35.275

2.5422

2.5486

0.240

299

225

4.1

4.84

36.055

2.4890

2.4952

0.280

202

228

2.8

3.78

36.910

2.4333

2.4393

0.320

169

234

2.3

0.90

37.160

2.4175

2.4235

0.120

216

234

3.0

2.14

37.680

2.3853

2.3912

0.240

240

237

3.3

1.58

39.435

2.2831

2.2888

0.280

449

246

6.1

2.67

39.675

2.2698

2.2755

0.080

396

246

5.4

0.82

40.325

2.2347

2.2403

0.160

520

250

7.1

0.95

40.930

2.2031

2.2086

0.120

480

253

6.6

2.66

41.445

2.1769

2.1823

0.240

372

256

5.1

2.65

41.990

2.1499

2.1552

0.120

538

259

7.4

1.31

42.670

2.1172

2.1225

0.160

428

262

5.9

1.45

43.145

2.0950

2.1002

0.120

433

266

5.9

1.50

44.190

2.0478

2.0529

0.160

376

269

5.1

0.89

46.095

1.9675

1.9724

0.160

279

279

3.8

0.86

46.510

1.9509

1.9558

0.240

310

282

4.2

0.87

48.305

1.8826

1.8872

0.200

506

292

6.9

2.06

48.900

1.8610

1.8657

0.240

615

296

8.4

1.67

50.330

1.8115

1.8160

0.160

437

303

6.0

1.73

51.035

1.7881

1.7925

0.080

416

306

5.7

0.93

53.550

1.7099

1.7141

0.480

177

317

2.4

2.84

54.500

1.6823

1.6865

0.400

130

324

1.8

1.37

55.420

1.6565

1.6606

0.320

130

328

1.8

1.72

56.220

1.6348

1.6389

0.320

121

331

1.7

0.87

56.770

1.6203

1.6243

0.240

142

335

1.9

1.59

57.405

1.6039

1.6079

0.240

112

339

1.5

1.19

58.500

1.5764

1.5804

0.240

67

342

0.9

1.57

12 ) A polymorph of flibanserin 1 characterized by having an X-ray powder diffraction pattern as shown in FIG. 1 .

13 ) A method for treating a disease that is treatable with a compound having an affinity for the 5-HT 1A or 5-HT 2 -receptors in a patient, comprising administering to said patient a therapeutically effective amount of form A according to claim 1 .

14 ) A method for treating a disease that is treatable with a compound having an affinity for the 5-HT 1A or 5-HT 2 -receptors in a patient, comprising administering to said patient a therapeutically effective amount of flibanserin 1 according to claim 2 .

15 ) A method for treating a disease that is treatable with a compound having an affinity for the 5-HT 1A or 5-HT 2 -receptors in a patient, comprising administering to said patient a therapeutically effective amount of a polymorph of flibanserin 1 according to claim 11 .

16 ) A method for treating a disease that is treatable with a compound having an affinity for the 5-HT 1A or 5-HT 2 -receptors in a patient, comprising administering to said patient a therapeutically effective amount of a polymorph of flibanserin 1 according to claim 12 .

17 ) A method for treating a disease selected from depression, schizophrenia, Parkinson's, anxiety, sleep disturbances, sexual and mental disorders and age associated memory impairment in a patient, comprising administering to said patient a therapeutically effective amount of form A according to claim 1 .

18 ) A method for treating a disease selected from depression, schizophrenia, Parkinson's, anxiety, sleep disturbances, sexual and mental disorders and age associated memory impairment in a patient, comprising administering to said patient a therapeutically effective amount of flibanserin I according to claim 2 .

19 ) A method for treating a disease selected from depression, schizophrenia, Parkinson's, anxiety, sleep disturbances, sexual and mental disorders and age associated memory impairment in a patient, comprising administering to said patient a therapeutically effective amount of a polymorph of flibanserin 1 according to claim 11 .

20 ) A method for treating a disease selected from depression, schizophrenia, Parkinson's, anxiety, sleep disturbances, sexual and mental disorders and age associated memory impairment in a patient, comprising administering to said patient a therapeutically effective amount of a polymorph of flibanserin 1 according to claim 12 .

21 ) A pharmaceutical composition comprising form A according to claim 1 , optionally in admixture with one or more pharmaceutical carriers, diluents or excipients.

22 ) A pharmaceutical composition comprising flibanserin 1 according to claim 2 , optionally in admixture with one or more pharmaceutical carriers, diluents or excipients.

23 ) A pharmaceutical composition comprising a polymorph of flibanserin 1 according to claim 11 , optionally in admixture with one or more pharmaceutical carriers, diluents or excipients.

24 ) A pharmaceutical composition comprising a polymorph of flibanserin 1 according to claim 12 , optionally in admixture with one or more pharmaceutical carriers, diluents or excipients.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2012
From: BIDACHEM S.P.A
To: SPROUT PHARMACEUTICALS, INC.
Reel/Frame 027527/0855 →