NZ275121A - N-[[[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio] ethyl]amino]methylene]-4-bromo-benzenesulphonamide, and medicaments - Google Patents

Description

New Zealand No. 275121 International No. PCT/ESS4/00109 TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION Priority dates: Complete Specification Filed: 04.11.1994 Classification:^) C07D277/48; A61K31/425 Publication date: 24 June 1997 Journal No.: 1417 NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION Title of Invention: Forms A and B of N-[[[2-[I[2-[(diaminomethylen)amino]-4-thiazolyl] methyl]thio]ethyl]amino]methylen]-4- bromobenzenosulphonamide Name, address and nationality of applicant(s) as in international application form: FERRER INTERNACIONAL SA, a Spanish company of Gran Via Carlos III, 94, ES-08028 Barcelona, Spain New Zealand No. 275121 International No. PCT/ES94/00109 NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION Title of Invention: Forms A and B of N-[[[2-[[[2-$diaminomethylen)amino]-4-thiazolyl] methyl]thio]ethyl]amino]methylen}-4- bromobenzenosulphonamide Name, address and nationality of applicant(s) as in international application form: FERRER INTERNACIONAL SA, a Spanish company of Gran Via Carlos III, 94, ES-08028 Barcelona, Spain 275121 ^ i I,, ■— T N.Z. PATEfc"' '[ 13 JUM ra" J" BSC61VED l^jesffw FORMS A AMD B OF N- f f t2 - f f T2 - T (DIAMINOMETHYLENE) AMINOI -4 -THIAZOLYL]METHYL] THIOl ETHYLl AMINO] METHYLEMEl -4-BROMO-BENZENESULFONAMIDE The present invention relates to novel Forms A and B of N-t t[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl] thio]ethyl]]amino]methylene]-4-bromo-benzenesulfonamide compound known as ebrotidine (WHO).

Brief description of the drawings Figure 1 is an infrared (IR) spectrum of ebrotidine Form A.

Figure 2 is an X-ray powder diffractogram of a) Ebrotidine Form A. b) Ebrotidine Form B.

Figure 3 is a differential scanning calorimetry (DSC) thermogram of Ebrotidine Form A.

Figure 4 is a infrared (IR) spectrum of Ebrotidine Form B.

Figure 5 is a differential scanning calorimetry (DSC) thermogram of Ebrotidine Form B. 2 Detailed description of the Invention N-[[[2- t [ [2 - t (diaminomethylene)amino]- 4 -thiazolyl] methyl]thio]ethyl] amino]methylene]-4-bromobenzenesulfonamide, 5 ebrotidine, is a compound which is active as a histamine H2-receptor antagonist, thus becoming useful in therapy as an acid secretion inhibitor. The preparation of this compound was disclosed in European Patent No. 0159012 and US Patent No. 4728655. The applicants have found out that ebrotidine 10 exhibits two novel forms, A and B, having a melting point in the range of 74-78°C and 142.5-146°C respectively. The present invention provides a process for obtaining selectively Forms A and B of ebrotidine. In the aforesaid patents, ebrotidine was obtained with a melting point of 107-15 110°C. By performing the same experimental method in those patents (Example 23 in both of them), the applicants have found out in the course of different crystallization assays that if to the methanol filtrate resulting from the reaction between [4- [ [ (2-aminoethyl) thio]methyl] -2-thiazolyl] guanidine 20 and ethyl 4-bromobenzene-sulfonyl-formimidate is added isopropanol and allowed to crystallize, ebrotidine isopropanolate is obtained, which is a useful intermediate for the preparation of Forms A and B of ebrotidine. Thus, the applicants have found out that Form A of ebrotidine can be 25 obtained in a pure state by treating ebrotidine isopropanolate with a mixture of methanol and water. Treatment of the obtained Form A of ebrotidine with methanol N.Z. PATENT office 1 3 JUN 1996 f1£CElV€D 3 leads to Form B of ebrotidine in a pure staJte. In turn, if Form B of ebrotidine is preferred to be obtained directly from the methanol solution, which is obtained according to the experimental method in the aforesaid example, the medium 5 may be seeded with crystals of Form B, thus constituing an extremely practical variation.

Forms A and B of ebrotidine have different properties. Form A is an amorphous solid and Form B is a crystalline 10 solid. Therefore, Form A is useful to prepare formulations that do not require any compression, such as capsules or sachets, while Form B is useful to prepare tablets. In case that the formulations to be prepared are liquid, the use of either form will be different since the proper 15 characteristics of the solid state are lost in solution.

Forms A and B of ebrotidine mixed with pharmaceutically acceptable carriers can be administered at daily doses ranging from 50 to 2000 mg.

The following examples illustrate the preparation of Forms A and B of ebrotidine, and pharmaceutical formulations containing them. The examples are not intended to 1imitate the scope of the invention as defined hereinabove or as 25 claimed below. n.z. patent office 1 3 Hjftl 1996 ^yamplPi 1 N-[[[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl] thio]ethyl]amino]methylene]- 4-bromo-benzenesulfonamide isopropanolate (Ebrotidine isopropanolate) To a suspension of 44.04 g of [4- [ [(2-aminoethyl) thio]methyl]-2-thiazolyl]guanidine dihydrochloride in 100 ml of methanol, 145 ml of 2.05 M methanol potassium hydroxide are added at a temperature below 20°C. To the resultant solution, 42.3 g of ethyl 4-bromobenzene-sulfonyl-formimidate are added at room temperature and the mixture is stirred for 1 hour, cooled at 0-5°C and filtered. To the filtrate, 245 ml of isopropanol are added at room temperature, and allowed to crystallize for 24 hours to yield 57.9 g of N-[[[2-[[[2-t (diaminomethylene)amino] - 4 - thiazolyl] methyl] thio] thyl] amino]methylene]-4-bromo-benzenesulfonamide isopropanolate having the following physico-chemical properties: Melting point: 96-98°C.

IR (KBr) cm'1: 3450 (NH2) , 3380 (NH2) , 1605 (C=N) , 1300 (S02) and 1180 (S02) .

'H-NMR (DMSO) 6 : 1.05 (d, 6H, (CH3) 2CH2OH) , 2.6 (t, 3H, -S-CH2-CH2) , 3.4 (m, 2H, -S-CH2-CH2) , 3.54 (s, 2H, het-CH2-S) , 3.8 (m, 2H, (CHj)2CH2OH) , 6.39 (s, 1H, thiazol) , 6.85 (wide, 4H, guanidine), 7.7 (s, 4H, aromatic), 8.15 (s, 1H, NH-CH=N) , 9.05 (wide, 1H, -NH-CH=) . nx PATENT office 1 3 JUN 1996 L RECEIVED IgTrampI e 2 N-[[[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl] methyl] thio] ethyl] amino]methylene] -4-bromobenzenesulfonamide Form A (Ebrotidine A form) 57.9 g of N-t[[2 -[[[2-[(diaminomethylene)amino]-4-thiazolyl ] methyl] thio] ethyl] amino] methylene] - 4 - bromo-benzenesulf onamide isopropanolate are dissolved in 87 ml of methanol at a temperature ranging between 40 and 50°C. The resultant solution is allowed to stand till a certain degree of turbidness fades away, then filtered and poured onto 550 ml of water at 0-5°C for 4 hours under energic stirring. After the addition is completed, the mixture is stirred for further 4 hours at 0-5°C and filtered. The filtrate is washed with abundant water and dried in vacuo at a temperature below 30°C to yield 49.9 g of ebrotidine Form A.

Melting point: 74-76°C.

IR (KBr) spectrum: Fig. 1 X-ray diffractogram: Fig. 2a.

Differential scanning calorimetry thermogram; Fig. 3..

N.Z. fVT-'-./r 13 JUN (996 RECEIVED Exampple 3 - V N-[[[2-[[[2-[(diaminomethylene)amino]-4-thiazolyl] methyl] thio] ethyl] amino] methylene] -4-bromobenzenesulf onamide Form B (Ebrotidine Form B) a) 49.9 g of ebrotidine Form A are poured onto 245 ml of methanol at 30°C. The resultant suspension is heated at 50-60°C for 1 hour, and then cooled at room temperature and stirred for 2 hours to yield a solid. The solid is filtered to give 41.9 of ebrotidine Form B.

Melting point: 142.5-146°C.

IR (KBr) spectrum: Fig. 4.

X-ray diffractogram: Fig. 2b.

Differential scanning calorimetry thermogram: Fig. 5. b) To the filtered methanol solution described in Example 1, some crystals of ebrotidine Form B are added and stirred for 24 hours at room tmperature to give 37 g of ebrotidine Form B under the same physicochemical properties of section a). 7 R-irampI P» 4 Monodose sachets Composition for each 400 mg monodose sachet: Ebrotidine Form A 400 mg Ammonium glycyrrhizinate %.. . 120 mg Silicon dioxide 30 mg Aspartame 20 mg Corn starch 1600 mg Scent 80 mg Sugar to volume 5000 mg Example 5 Coated tablets Composition for each 400 mg coated tablet: Ebrotidine Form B 400 mg Croscarmellose sodium 30 mg Silicon dioxide 4 mg Magnesium stearate 12 mg Talc 60 mg Microcrystalline cellulose 30 mg Aminoethylmethacrylate copolymer and neutral esters of mathacrylic acid.. 8 mg Titanium dioxide 8 mg Polyethylene glycol 6000. . . 2 mg n.Z. PATENT office 1 3 JUN 1996 RECEIVED 275121

Claims (7)

WHAT WE CLAIM IS:

1) - A compound of the chemical name N-[[[2-[[[2-[ (diaminomethylene) amino] -4 - thiazolyl] methyl] thio] ethyl] amino]methylene] -4-bromo-benzenesulfonamide in Form A. *-m

2) - A compound of the chemical name N-[[[2-[[[2-[ (diaminomethylene) amino] -4 - thiazolyl] methyl] thio] ethyl] amino]methylene] -4-bromo-benzenesulfonamide in Form B*.

3) - A compound according to claim 1 having a melting point in the range 74-78°C, the IR spectrum as shown in Figure 1, the x-ray diffractogram as shown in Figure 2a and the differential scanning calorimetry thermogram as shown in Figure 3.

4) - A compound according to claim 2 having a melting point in the range 142.5-146°C, the IR spectrum as shown in Figure 4, the x-ray diffractogram as shown in Figure 2b and the differential scanning calorimetry thermogram as shown in Figure 5.

5) - A process for preparing Form A *of N-[[[2-[[[2-[ (diaminomethylene) amino] - 4-thiazolyl]methyl] thio] ethyl] amino]methylene]-4-bromo-benzenesulfonamide which comprises reacting [4 -[[(2-aminoethyl)thio]methyl]-2 -thiazolyl] guanidine dihydrochloride with ethyl 4-brc * (as hereinbefore defined) 17 512|j 9 sulfonyl- formimidate in methanol and in the presence of potassium hydroxide, followed by filtration and addition of isolapropanol over the filtrate, the intermediate N-[[[2-[[ [2-[(diaminomethylene)amino]-4-thiazolyl]methyl] thio]ethyl] amino]methylene]-4-bromo-benzenesulfonamide is obtained which, by dissolving in methanol, filtering, and adding the filtrate to water leads to the aforesaid Form A.

6) - A process for preparing Form B*of N-[[[2-[[[2-[ (diaminomethylene) amino] -4 - thiazolyl] methyl ] thio] ethyl] amino]methylene]-4-bromo-benzenesulfonamide which comprises pouring Form A#of said compound over methanol, followed by heating the resultant suspension at 50-60°C and subsequent cooling at room temperature.

7) - A process for preparing Form B *of N-[[[2-[[[2-[ (diaminomethylene) amino] -4 - thiazolyl] methyl ] thio] ethyl] amino]methylene]-4-bromo-benzenesulfonamide which comprises seeding some crystals of said compound on the filtrate of the methanol medium, where the reaction between [4-[ [ (2-amino-ethyl) thio] methyl ] - 2 - thiazolyl ] guanidine dihydrochloride and ethyl 4-bromo-benzene-sulfonyl-formimidate occurs according to claim 5, and subsequent stirring at room temperature. * (as hereinbefore defined) tsy mo uuioonttci agents END OF CLAIMS