IP Library › Granted Patent US 11,021,474
Granted Patent B2
US 11,021,474 · App. 16/464,448 · Granted Jun 1, 2021

N-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)-phenyl]-acetamide free base hemihydrate, methods of manufacture and uses thereof

Inventors: Yogeshwar Bachhav (Mumbai, IN); Wilfried Schwab (Werder, DE); Alexander Birkmann (Wuppertal, DE); Kurt Voegtli (Oberhofen AG, CH)
Assignee: AiCuris Anti-Infective Cures GmbH
C07D417/12
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,021,474
App. No.
16/464,448
Granted
Jun 1, 2021
Kind
B2
Abstract

The present invention relates to the field of anti-viral active agents, particularly the free base hemihydrate form of N-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)-phenyl]-acetamide as well as methods for the manufacture thereof. The present invention relates also to the use of the above compound in the treatment of human herpes virus infections and in the preparation of pharmaceuticals comprising said compound.

Claims (25)

1. A N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate having the molecular formula C 18 H 18 N 4 O 3 S 2 ×0.5H 2 O.

2. The N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate according to claim 1 , which comprises XRPD peaks at 5.9, 11.7, 15.5 and 18.7.

3. A pharmaceutical composition comprising N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate according to claim 1 , wherein said composition further comprises at least one pharmaceutically acceptable excipient.

4. A pharmaceutical composition obtained by formulating the N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate as defined in claim 1 with at least one pharmaceutically acceptable excipient.

5. The pharmaceutical composition as defined in claim 3 , wherein the N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate is present in an amount of about 0.1 to about 10% w/w.

6. A medicament composition comprising N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate according to claim 1 .

7. A method for the treatment of herpes virus infection, which comprises administering to a subject in need thereof a composition comprising the N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate as defined in claim 1 .

8. The method of claim 7 , wherein the herpes virus is selected from the order of simplex viruses.

9. A method according to claim 8 , wherein the herpes virus infection is selected from recurrent herpes labialis, herpes genitalis, herpes keratitis, herpes meningitis, herpes encephalitis, or herpes infections in a newborn.

10. A method of manufacturing N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide free base hemihydrate as defined in claim 1 , wherein said method comprises the following steps:

a) Mixing 4-pyridine-2yl-phenyl)-acetic acid and amionothiazole sulfonic acid amide in N-Methylpyrorrolidone (NMP);

b) Cooling the mixture obtained in step a);

c) Adding N-Ethyl-N′-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC×HCl) to said mixture obtained in step b);

d) Stirring the solution obtained in step c) and addition to purified H 2 O;

e) Filtering the solution obtained in step d);

f) Washing the product cake obtained in step e);

g) Drying the product obtained in step f);

h) Adding H 2 O to the solution obtained in step g);

i) Stirring the suspension obtained in step h);

j) Cooling the suspension obtained in step i);

k) Stirring the suspension obtained in step j);

l) Isolating the product by filtration of the suspension obtained in step k);

m) Washing the product obtained in step l) with H 2 O;

n) Drying the product obtained in step m).

11. A pharmaceutical composition comprising a free base hemihydrate of N-[5-(amino-sulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide obtained by a method according to claim 10 .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2024
From: AICURIS GMBH & CO. KG
To: AIC316 GMBH
Reel/Frame 069351/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: AICURIS ANTI-INFECTIVE CURES GMBH
To: AICURIS GMBH & CO. KG
Reel/Frame 052640/0562 →
CHANGE OF NAME Recorded Oct 9, 2019
From: PIRAMAL IMAGING SA
To: LIFE MOLECULAR IMAGING SA
Reel/Frame 050668/0158 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: BACHHAV, YOGESHWAR; SCHWAB, WILFRIED; BIRKMANN, ALEXANDER; VOEGTLI, KURT
To: AICURIS ANTI-INFECTIVE CURES GMBH
Reel/Frame 049654/0716 →
Priority Claims (1)
EP 16200967 · Nov 28, 2016 · regional
Continuity (1)
Related Publication 20200123145A1 · Apr 23, 2020
Cited By (1)
US 12,740,971