NZ762057B2 - Fluoropiperidine compounds as pure 5-ht6 receptor antagonists - Google Patents

Abstract

The present invention relates to fluoropiperidine compounds of formula (I), their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof as 5-HT6 receptor antagonists. In particular the present invention discloses the methods of preparation, pharmaceutical composition, combinations and use of fluoropiperidine compounds, their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof. In formula (I), R1 represents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups selected from halogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R2 represents hydrogen or (C1-6)-alkyl; R3 represents hydrogen or (C1-6)-alkyl; or R2 and R3 can combine together to form (C3-6)-cycloalkyl; R4 represents hydrogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R5 represents hydrogen, (C1-6)-alkyl, halo(C1-6)-alkyl or -(CH2)0-3-(C3-6)-cycloalkyl. The compounds can be used in the treatment of cognitive disorder mediated by the 5-Hydroxytryptamine 6 receptor, wherein said cognitive disorder is selected from the group consisting of dementia in Alzheimer's disease, dementia in Parkinson's disease, dementia in Huntington's disease, dementia associated with Down syndrome, dementia associated with Tourette's syndrome, dementia associated with post menopause, frontotemporal dementia, Lewy body dementia, Vascular dementia, dementia in HIV, dementia in Creutzfeldt-Jakob disease, substance-induced persisting dementia, dementia in Pick's disease, dementia in schizophrenia, dementia in general medical conditions and senile dementia. ns and use of fluoropiperidine compounds, their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof. In formula (I), R1 represents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups selected from halogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R2 represents hydrogen or (C1-6)-alkyl; R3 represents hydrogen or (C1-6)-alkyl; or R2 and R3 can combine together to form (C3-6)-cycloalkyl; R4 represents hydrogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R5 represents hydrogen, (C1-6)-alkyl, halo(C1-6)-alkyl or -(CH2)0-3-(C3-6)-cycloalkyl. The compounds can be used in the treatment of cognitive disorder mediated by the 5-Hydroxytryptamine 6 receptor, wherein said cognitive disorder is selected from the group consisting of dementia in Alzheimer's disease, dementia in Parkinson's disease, dementia in Huntington's disease, dementia associated with Down syndrome, dementia associated with Tourette's syndrome, dementia associated with post menopause, frontotemporal dementia, Lewy body dementia, Vascular dementia, dementia in HIV, dementia in Creutzfeldt-Jakob disease, substance-induced persisting dementia, dementia in Pick's disease, dementia in schizophrenia, dementia in general medical conditions and senile dementia.

Description

The t invention relates to fluoropiperidine compounds of formula (I), their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof as 5-HT6 receptor nists.

In particular the present invention discloses the methods of preparation, pharmaceutical composition, combinations and use of fluoropiperidine compounds, their stereoisomers, ic forms or pharmaceutically acceptable salts thereof. In formula (I), R1 represents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups ed from halogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R2 represents hydrogen or (C1-6)-alkyl; R3 represents hydrogen or (C1-6)-alkyl; or R2 and R3 can combine together to form -cycloalkyl; R4 represents hydrogen, (C1-6)-alkyl or halo(C1-6)-alkyl; R5 represents en, (C1-6)-alkyl, halo(C1-6)-alkyl or 0(C3-6)-cycloalkyl. The compounds can be used in the treatment of cognitive er mediated by the 5-Hydroxytryptamine 6 receptor, wherein said cognitive disorder is selected from the group consisting of dementia in Alzheimer's disease, dementia in Parkinson's e, dementia in Huntington's disease, dementia associated with Down syndrome, dementia associated with te's syndrome, dementia associated with post menopause, frontotemporal dementia, Lewy body dementia, Vascular dementia, dementia in HIV, dementia in Creutzfeldt-Jakob disease, nce-induced persisting dementia, dementia in Pick's disease, dementia in schizophrenia, dementia in general medical conditions and senile dementia. 762057 B2 FLUOROPIPERIDINE COMPOUNDS AS PURE 5-HT6 RECEPTOR ANTAGONISTS FIELD OF THE INVENTION The present invention relates to fluoropiperidine nds, their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof as 5—Hydroxytryptamine 6 receptor (5—HT6R) antagonists. In particular the present invention ses the methods of preparation, pharmaceutical composition, combinations and use of iperidine compounds, their stereoisomers, isotopic forms or pharmaceutically acceptable salts thereof.

BACKGROUND OF INVENTION The disturbance in the neurotransmitter, 5—hydroxytryptamine (5—HT) or serotonin was implicated in various l nervous system disorders such as anxiety, depression, neurodegenerative ers, cognitive disorders or motor dination disorders.

Serotonin is localized in the central and peripheral nervous systems (CNS & PNS) and is known to play a vital role in many ical processes. The up regulation or de—regulation of it is involved in conditions including cognitive disorders, psychiatric disorders, motor incoordination, feeding behavioral disorders, sexual disorders, neuroendocrine regulation disorders and among others. The 5—HT receptor subtypes include 5—HT1, 5—HT; 5—HT3, 5— HT4, 5—HT5, 5—HT6, 5—HT7 and the isoforms such as 5—HT2A, 5—HTZB, , 5—HT4A, 5— HT4B, 5-HT4D and 5-HT4E.

The 5—Hydroxytryptamine 6 or R) subtype was first identified in 1993 and is a member of GPCR family. The 5—HT6R is almost exclusively expressed in the brain, particularly in hippocampus and frontal cortex which are associated with cognition (Molecular cology, 1993, 43, 320—327). Activation of 5—HT6R usually represses cholinergic function (British Journal of Pharmacology, 1999, 126, 1537—1542), whereas blockade of the receptor improves the cognitive functions.

Recent studies have shown that antagonism of this or by several investigational compounds improved learning and memory in animal models (CNS & ogical Disorders - Drug Targets, 2004, 3, 59—79). Therefore, the antagonism of the —HT6 receptor can potentially provide an effective treatment for different cognitive disorders.

The US7378415 patent disclosed the benzoxazine and quinoxaline compounds, as shown below, having 5—HT6 and 5—HT2A receptor affinity for the treatment of certain CNS disorders.

The clinical candidates, Idalopirdine (Lu AE58054) and Cerlapirdine (SAM—531), which are 5—HT6R antagonists and also showed affinity towards 5—HT2A receptors, are discontinued from the clinical trials.

Therefore, the aim of the present invention is to provide the nds having potent 5—HT6 receptor affinity with minimal or no affinity s 5—HT2A receptor and also to provide the nds having good safety profile. The instant invention es the fluoropiperidine compounds that are highly selective towards 5—HT6 receptor with minimal or no affinity towards 5—HT2A receptor. A person ordinary skilled in the art would not have thought that the introduction of specific group (fluoro) at a ic position of the fluoropiperidine derivatives will result in improvement of selectivity over 5—HT2A receptor and possess better safety profile. These observations were highly surprising and unexpected.

SUMMARY OF THE INVENTION In first aspect, the present ion relates to fluoropiperidine compound of formula (I), o 0 O\|s—/ R3 wherein: WO 30641 R1 represents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups ed from halogen, (C1_6)—alkyl or 1_6)—alkyl; R2 ents hydrogen or (C1_6)—alkyl; R3 represents hydrogen or (C1_6)—alkyl; or R2 and R3 can combine together to form (C3_6)— cycloalkyl; R4 represents hydrogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R5 represents hydrogen, (C1_6)—alkyl, halo(C1_6)—alkyl or —(CH2)0-3—(C3_6)—cycloalkyl; or a isomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In another aspect, the present invention relates to the processes for preparing the compound of formula (I), or a stereoisomer or an isotopic form, or a pharmaceutically acceptable salt thereof.

In yet another aspect, the present invention relates to pharmaceutical composition containing a therapeutically effective amount of at least one nd of a (I), or a stereoisomer or an isotopic form, or a pharmaceutically acceptable salt thereof and pharmaceutically acceptable ents or carriers.

In yet another aspect, the t ion relates to the combination of compound of formula (I) or a pharmaceutical salt f, an acetylcholinesterase inhibitor and a NMDA receptor antagonist, for use in the treatment of cognitive disorders.

In yet another aspect, the present ion relates to the combination of compound of formula (I) or a pharmaceutical salt thereof and an acetylcholinesterase inhibitor, for use in the treatment of cognitive disorders.

In yet another aspect, the present ion relates to the ation of compound of formula (I) or a pharmaceutical salt thereof and a NMDA receptor antagonist, for use in the treatment of cognitive disorders.

In yet another aspect, the present invention relates to compound of formula (I), or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof, for use as 5— HT6 receptor antagonist.

In yet another aspect, the present invention relates to compound of formula (I), or a stereoisomer or an isotopic form or a ceutically acceptable salt thereof, for use in the treatment of cognitive disorders.

In another aspect, the present invention s to a method for the treatment of cognitive disorders, comprising administering to a patient in need thereof, a therapeutically effective amount of a compound of formula (I), or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In yet another aspect, the present invention relates to use of the compound of formula (I), or a stereoisomer, or an isotopic form or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment of cognitive disorders.

BRIEF DESCRIPTION OF THE DIAGRAMS Figure 1 depicts the effect of example 1 and donepezil combination on extracellular levels of acetylcholine in ventral hippocampus of male Wistar rats.

Figure 2 s the effect of example 1, zil and memantine ation on extracellular levels of choline in ventral hippocampus of male Wistar rats.

DETAILED DESCRIPTION OF THE INVENTION Unless otherwise stated, the following terms used in the specification and claims have the meanings given below: The term, "(C1_6)—alkyl" as used herein refers to ed or straight chain tic hydrocarbon containing 1 to 6 carbon atoms. Examples of (C1_6)—alkyl include methyl, ethyl, n—propyl, isopropyl, n—butyl, isobutyl, tyl, tert—butyl, pentyl and hexyl.

The term, "halogen" or "halo" as used herein refers to fluorine, chlorine, bromine or . Preferably, halogen is fluorine, ne or bromine. More preferably halogen is fluorine.

The term "halo(C1_6)—alkyl" as used herein refers to —alkyl as defined above wherein one or more hydrogens of the same or different carbon atom is tuted with same or different halogens. Examples of halo(C1_6)—alkyl include fluoromethyl, chloromethyl, fluoroethyl, difluoromethyl, dichloromethyl, trifluoromethyl, difluoroethyl, chlorofluoroethyl and the like.

The term, "(C3_6)—cycloalkyl" as used herein refers to saturated monocyclic hydrocarbon ring containing three to six carbon atoms. Examples of (C3_6)—cycloalkyl group include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

The phrase, "therapeutically effective amount" is defined as an amount of a compound of the present invention that (i) treats the particular disease, condition or disorder (ii) eliminates one or more symptoms of the particular e, condition or disorder (iii) attenuates the symptoms of the particular e, condition or disorder (iv) delays the onset of one or more symptoms of the particular disease, condition or disorder described herein.

The term, "isotopic form" as used herein refers to the compound of formula (I) n one or more atoms of compound of formula (I) are substituted by their respective isotopes. For example, isotopes of hydrogen include 2H (deuterium) and H (tritium).

The term, "stereoisomers" as used herein refers to isomers of compound of formula (I) that differ in the arrangement of their atoms in space. nds disclosed herein may exist as single stereoisomer, racemate and/or mixtures of enantiomers and/or diastereomers. All such single stereoisomer, tes and mixtures thereof are ed to be within the scope of the present invention.

The term, "pharmaceutically acceptable salt" as used herein refers to salts of the active compound Le. the compound of formula (I), and are prepared by reaction with the appropriate acid or acid derivative, depending on the ular substituents found on the compounds described herein.

The term, "cognitive er" as used herein refers to a group of mental health disorders that pally affect learning, memory, perception, m g, and include amnesia, dementia, and delirium. Cognitive disorders can be idiopathic or result due to disease, disorder, ailment or toxicity. Preferably the cognitive disorder mentioned here is ia. Examples of dementia includes but not limited to, dementia in Alzheimer's disease, ia in Parkinson's disease, dementia in Huntington's disease, dementia associated with Down syndrome, dementia associated with Tourette’s syndrome, dementia associated with post menopause, frontotemporal dementia, Lewy body ia, Vascular dementia, dementia in HIV, dementia in Creutzfeldt—Jakob disease, substance— induced persisting dementia, dementia in Pick’s e, dementia in schizophrenia, dementia in general medical conditions and senile dementia.

EMBODIMENTS The present invention asses all the compounds described by the compound of formula (I) without any limitation, r, preferred aspects and elements of the invention are discussed herein in the form of the following embodiments.

In second aspect, the present invention relates to the compound of formula (I) o 0 0\l_/ R3 Rl/ \ wherein: R1 represents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups selected from halogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R2 represents hydrogen or (C1_6)—alkyl; R3 represents hydrogen or (C1_6)—alkyl; or R2 and R3 can combine together to form (C3_6)— cycloalkyl; R4 represents hydrogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R5 represents en, (C1_6)—alkyl, halo(C1_6)—alkyl or —(CH2)0-3—(C3_6)—cycloalkyl; or a stereoisomer or an isotopic form or a ceutically acceptable salt thereof.

In another aspect, the present invention relates to the nd of formula (Ia), derived from the compound of formula (I), O\\//0 R2 R1 R3 R5 (Ia) wherein: R1 ents phenyl or pyridyl; wherein the phenyl or pyridyl is optionally substituted with one or more groups selected from halogen, —alkyl or halo(C1_6)—alkyl; R2 represents hydrogen or (C1_6)—alkyl; R3 represents hydrogen or (C1_6)—alkyl; or R2 and R3 can combine er to form (C3_6)— cycloalkyl; R4 represents hydrogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R5 represents hydrogen, —alkyl, halo(C1_6)—alkyl or —(CH2)0-3—(C3_6)cycloalkyl; or a stereoisomer, or an isotopic form or a pharmaceutically acceptable salt thereof.

In another aspect, the present invention relates to the compound of formula (Ib), derived from the compound of formula (I), S N // \\ R4 O O wherein: R1 represents phenyl or pyridyl; n the phenyl or pyridyl is optionally substituted with one or more groups selected from halogen, (C1_6)—alkyl or 1_6)—alkyl; R2 represents hydrogen or (C1_6)—alkyl; R3 represents hydrogen or (C1_6)—alkyl; or R2 and R3 can combine together to form (C3_6)— cycloalkyl; R4 ents hydrogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R5 represents hydrogen, (C1_6)—alkyl, halo(C1_6)—alkyl or 0_3—(C3_6)—cycloalkyl; or a stereoisomer, an isotopic form or a pharmaceutically able salt thereof.

In another aspect, the present invention relates to the nd of formula (I), n: R1 represents phenyl optionally substituted with one or more groups selected from halogen, (C1_6)—alkyl or halo(C1_6)—alkyl; or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In another aspect, the present invention relates to the nd of formula (I), wherein R1 represents pyridyl optionally substituted with one or more groups selected from halogen, (C1_6)—alkyl or halo(C1_6)—alkyl; or a isomer, or an isotopic form, or a pharmaceutically acceptable salt thereof.

In r aspect, the present invention relates to the compound of formula (I), wherein: R1 represents phenyl or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In r aspect, the t invention relates to the compound of formula (I), 0 o O\s| / R3 / I R1 \ wherein: R1 represents phenyl optionally substituted with one or more groups selected from halogen, (C1_6)—alkyl or halo(C1_6)—alkyl; R2 represents en; R3 represents hydrogen; R4 represents hydrogen or (C1_6)—alkyl; R5 represents hydrogen; or a stereoisomer, an isotopic form or a pharmaceutically acceptable salt thereof.

In another embodiment, the compound of the invention is selected from the group consisting of: 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4] oxazine; 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4] oxazine; luoropiperidin—4—yl)—7—(pyridine—2—sulfonyl)—3,4—dihydro—2H—benzo[l,4]oxazine; 4—(3—Fluoropiperidin—4—yl)—7—(pyridine—4—sulfonyl)—3,4—dihydro—2H—benzo[l,4]oxazine; 7—Phenylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4] oxazine; 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine; and 7—Phenylsulfonyl—4— [3—fluoro— l —(2—fluoroethyl)piperidin—4—yl] —3 ,4—dihydro—2H— benzo[ l ,4] e; or a stereoisomer or a pharmaceutically acceptable salt thereof.

In another embodiment, the preferred compound of the invention is selected from the group consisting of: Racemic—7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine; 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine (Peak I); ylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine (Peak II); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[ l ,4]oxazine (Peak III); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine (Peak IV); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak I); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak II); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hloride (Peak III); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak IV); Racemic—7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H— benzo[ l ,4] oxazine; 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine (Peak I); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine (Peak II); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine (Peak III); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine (Peak IV); luorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak I); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hloride (Peak II); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak III); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak IV); Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—2—sulfonyl)—3,4—dihydro—2H— benzo[ l ,4] oxazine; Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—2—sulfonyl)—3,4—dihydro—2H— benzo[ l ,4] oxazine hydrochloride; Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—4—sulfonyl)—3,4—dihydro—2H— benzo[l,4]oxazine; Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—4—sulfonyl)—3,4—dihydro—2H— benzo[ l ,4] oxazine hydrochloride; Racemic—7—Phenylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3,4—dihydro—2H— benzo[ l ,4] oxazine; ylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (First eluting ); 7—Phenylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Second eluting isomer); Racemic—6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine; Racemic—6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l zine hydrochloride; 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak I); 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak II); ylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak III); 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak IV); 7—Phenylsulfonyl—4— [3—fluoro— l uoroethyl)piperidin—4—yl] —3 ,4—dihydro—2H— benzo[ l ,4] oxazine (Peak III); 7—Phenylsulfonyl—4— [3—fluoro— l uoroethyl)piperidin—4—yl] —3 ,4—dihydro—2H— benzo[ l ,4]oxazine (Peak IV); or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In r embodiment, the preferred compound of the invention is selected from the group consisting of: 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak III); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak I); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak II); 7—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Peak IV); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hloride (Peak 1); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak 11); luorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak III); 7—(3—Fluorophenylsulfonyl)—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4]oxazine hydrochloride (Peak IV); Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—2—sulfonyl)—3,4—dihydro—2H— benzo[ l ,4] oxazine hydrochloride; Racemic—4—(3—Fluoropiperidin—4—yl)—7—(pyridine—4—sulfonyl)—3,4—dihydro—2H— benzo[ l ,4] oxazine hydrochloride; 7—Phenylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hloride (First eluting isomer); 7—Phenylsulfonyl—4—(3—fluoro—3—methylpiperidin—4—yl)—3 ,4—dihydro—2H—benzo[ l ,4]oxazine hydrochloride (Second eluting isomer); c—6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3 ydro—2H—benzo[ l zine hydrochloride; 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak 1); 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak 11); 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak III); 6—Phenylsulfonyl—4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[l,4] oxazine (Peak IV); 7—Phenylsulfonyl—4— [3—fluoro— l —(2—fluoroethyl)piperidin—4—yl] —3 ,4—dihydro—2H— benzo[l,4]oxazine (Peak III); and 7—Phenylsulfonyl—4— [3—fluoro— l uoroethyl)piperidin—4—yl] —3 ,4—dihydro—2H— benzo[ l ,4]oxazine (Peak IV); or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

Experimental Procedures: The scheme—l depicts the general process for preparation of the compounds of formula (1), wherein R1, R2, R3, R4 and R5 are as defined in the first aspect.

Scheme-1 \ / \ / \ / \ N02 R1 No2 No2 R1 NH2 (1 ) (2) (3) (4) 0°" / O O O O Step4 /S_\ I Step5 O¢§_/ Step—6 O¢§_/ R3 ' I I R1 NH i R4 1/ \ NH R1/ \ N F R4 R4 F F (6) l" (7) N (8) N BOC I I Boo Boo 2 R2 0 o O O O‘g—\ / fR3 OQII / 3 Step—7 | Step—8 S— | —> / \ _> 1/ \ TR 1 N N R4 R4 N N Fll5 Fli5 Compound of formula (I) Compound of formula (I) wherein R5 is H wherein R5 is (C1_G)—alkyl, na|o(C1_6)—a|kyl, —(CH2)0_3—(03—6) Cycloalkyl Step-1: Preparation of compound of formula (2) The compound of formula (1) is reacted with a compound, RISH (wherein R1 is as defined in first aspect) in presence of base selected from um carbonate, cesium carbonate, potassium carbonate and sodium carbonate in solvent selected from dimethlylsulfoxide (DMSO), dichloromethane (DCM), tetrahydrofuran (THF), acetonitrile (ACN) and dimethylformamide (DMF) at the temperature in the range of 25—3OOC for 2 to 4 hours to obtain the compound of a (2).

Step-2: Preparation of compound of formula (3) The compound of formula (2) obtained in step—1 is reacted with ing agent such as hloroperoxybenzoic acid (mCPBA) or oxone in the solvent selected from DCM, chloroform (CHC13), toluene at the temperature in the range of C for 22 to 26 hours to obtain the compound of formula (3).

Step-3: Preparation of compound of formula (4) The nitro group in compound of formula (3) ed in step—2 is reduced with Fe/NH4C1, zinc/acetic acid, or NiC1 in presence of a mixture of solvents such as anolzwater under room temperature to reflux conditions for 2 to 6 hours to obtain the compound of formula (4).

Step-4: Preparation of compound of formula (6) The compound of formula (4) obtained in step—3 is reacted with the compound of formula (5), under reductive amination conditions using reducing agents such as sodium triacetoxyborohydride, sodium orohydride, sodium borohydride in the solvents selected from DCM, dichloroethane (EDC), CHC13, methanol, acetic acid and toluene at the temperature in the range of 25—30°C for 22 to 26 hours to obtain the compound of formula (6).

: Preparation of compound of formula (7) The compound of formula (6) obtained in step—4 is d with the compound of a (A), R2 R3 )Q/Cl in presence of iodinating agents such as sodium iodide and tetrabutylammonium iodide and base such as ium ate, sodium carbonate, cesium carbonate in the solvent selected from DCM, THF, ACN and DMF under room temperature to reflux conditions for 4 to 8 hours to obtain the compound of formula (7).

Step-6: Preparation of compound of formula (8) The nd of formula (7) obtained in step—5 is cyclized using sodium iodide or tetra—butyl ammonium iodide and potassium carbonate, cesium carbonate, sodium hydride or sodium tert—butoxide in the solvent selected from THF, ACN and DMF at the temperature in the range of 25—30°C for 2 to 6 hours to obtain the compound of formula (8).

Step-7: Preparation of compound of formula (I) (wherein R5 is hydrogen) The compound of a (8) obtained in step—6 is subjected to tert— butyloxycarbonyl group removal using solvents such as methanol, ethanol, isopropanol, ethyl acetate, l,4—dioxan and acid such as hydrochloric acid, hydrobromic acid, oroacetic acid under room temperature to reflux conditions, for 2 to 6 hours, to obtain the compound of formula (I) (wherein R5 is hydrogen).

Step-8: Preparation of compound of formula (I) (wherein R5 is (C1_6)-alkyl, halo(C1_6)- alkyl or —(CH2)0_3-(C3_6)-cycloalkyl) The compound of formula (I) obtained in step—7 is optionally alkylated using formaldehyde/formic acid mixture, aldehydes, s, alkyl halides or cycloalkyl halides to obtain a compound of formula (I) (wherein R5 is (C1_6)—alkyl, halo(C1_6)—alkyl or — (CH2)0_3—(C3_6)—cycloalkyl).

Separation of enantiomers The diastereoisomers of compound of formula (8), compound of formula (I), are separated using chiral column chromatography separation to obtain the pure enantiomeric forms.

Preparation of pharmaceutically acceptable salt of compound of formula (I) The compound of formula (I) can optionally be ted into its ceutically acceptable salt by reaction with the appropriate acid or acid tive. Suitable pharmaceutically acceptable salts will be apparent to those skilled in the art. The salts are formed with inorganic acids e.g., hydrochloric, hydrobromic, sulfuric, perchloric & phosphoric acid or c acids e.g., oxalic, succinic, , acetic, fumaric, citric, malic, tartaric, benzoic, c, esulfonic, esulfonic acid, methanesulfonic or naphthalenesulfonic acid.

Scheme—2 depicts the process for preparation of compound of formula (3a).

Scheme-2 OH R1802CI,AICI3 \936go" N02 140 °C N02 (1a) (3a) The compound of formula (la) is reacted with l in presence of aluminum chloride at a temperature in the range of l30—lSOOC for 8 tol6 hours to obtain compound of formula (3a). The compound of formula (3a) can also be converted into compound of formula (I) by following the process in scheme—l, starting from step—3.

Preparation of stereoisomers of compound of formula (I) The stereoisomers of compounds of formula (I) may be prepared by one or more conventional ways presented below: a. One or more of the reagents may be used in their optically active form. b. Optically pure catalyst or chiral ligands along with metal catalyst may be employed in the reduction process. The metal catalyst may be rhodium, ium, indium and the like. The chiral ligands may ably be chiral phosphines.

C. The mixture of stereoisomers may be resolved by conventional methods such as forming diastereomeric salts with chiral acids or chiral amines or chiral amino alcohols, or chiral amino acids. The resulting mixture of diastereomers may then be separated by methods such as fractional crystallization, chromatography and the like, which is followed by an additional step of isolating the optically active product from the resolved material / salt. d. The mixture of stereoisomers may be resolved by conventional methods such as microbial resolution, resolving the diastereomeric salts formed with chiral acids or chiral bases. Chiral acids that can be employed may be tartaric acid, mandelic acid, lactic acid, camphorsulfonic acid, chiral amino acids and the like. Chiral bases that can be employed may be cinchona ids, brucine or a basic amino acid such as lysine, arginine and the like.

In another embodiment, the suitable pharmaceutically acceptable salt includes but not limited to hydrochloride, hydrobromide, oxalate, fumarate, tartrate, maleate and succinate.

In another aspect of the t invention, the compound of formula (I) are 5— Hydroxytryptamine 6 receptor (5—HT6R) antagonists.

In another aspect, the present invention relates to a method of treatment of cognitive ers comprising administering to a patient in need thereof, a therapeutically effective amount of compounds of formula (I) or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In r aspect, the present invention s to a method of treatment of cognitive ers including dementia in Alzheimer's disease, dementia in Parkinson's e, dementia in Huntington's disease, dementia associated With Down syndrome, dementia ated with Tourette’s syndrome, ia associated with post menopause, frontotemporal dementia, Lewy body dementia, Vascular dementia, dementia in HIV, dementia in Creutzfeldt—Jakob e, substance—induced persisting dementia, dementia in Pick’s disease, ia in schizophrenia, dementia in general medical ions and senile dementia comprising administering to a t in need thereof, a therapeutically effective amount of compounds of formula (I) or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof.

In yet another aspect, the present invention relates to nd of formula (I) or a stereoisomer or an isotopic form or a ceutically acceptable salt thereof, for use in the treatment of disease or disorder selected from cognitive disorders.

In yet another aspect, the present invention s to use of the compound of formula (I) or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof, in the manufacture of medicament for the treatment of cognitive disorders.

In yet r aspect, the present invention relates to use of the compound of formula (I) or a stereoisomer or an isotopic form or a pharmaceutically acceptable salt thereof, in the manufacture of medicament for the treatment of cognitive disorders.

In yet another embodiment, the present invention relates to the ation of compound of formula (I) or a pharmaceutical salt f, an acetylcholinesterase inhibitor and a NMDA receptor antagonist, for use in the treatment of cognitive disorders.

In yet another embodiment, the present invention relates to the combination of compound of formula (I) or a pharmaceutical salt thereof and an acetylcholinesterase inhibitor, for use in the ent of cognitive disorders.

In yet another embodiment, the present invention relates to the combination of compound of formula (I) or a pharmaceutical salt thereof and a NMDA receptor antagonist, for use in the ent of cognitive disorders.

In another embodiment, the present invention s to the combination wherein the acetylcholinesterase inhibitor is selected from galantamine, rivastigmine, donepezil and e or a pharmaceutically able salt thereof.

In another embodiment, the present invention relates to the combination wherein the acetylcholinesterase inhibitor in the combination is donepezil hydrochloride.

In r embodiment, the present invention relates to the combination wherein the NMDA receptor antagonist in the combination is memantine or a pharmaceutically acceptable salt thereof. In another embodiment, the present invention relates to the ation n the NMDA receptor antagonist in the combination is memantine hydrochloride.

In yet another aspect, the present invention relates to the pharmaceutical composition of the compound of a (I). In order to use the compound of formula (I), or their isomers and pharmaceutically acceptable salts thereof in therapy, they will normally be formulated into a pharmaceutical composition in accordance with standard pharmaceutical practice.

The pharmaceutical compositions of the present ion may be formulated in a conventional manner using one or more pharmaceutically acceptable ents. The pharmaceutically able ents are diluents, disintegrants, binders, lubricants, glidants, polymers, coating agents, solvents, cosolvents, preservatives, wetting agents, ning agents, antifoaming , sweetening agents, flavouring agents, antioxidants, colorants, solubilizers, plasticizer, dispersing agents and the like. Excipients are selected from microcrystalline ose, mannitol, lactose, pregelatinized starch, sodium starch glycolate, corn starch or derivatives thereof, ne, crospovidone, calcium te, glyceryl monostearate, glyceryl palmitostearate, talc, colloidal silicone dioxide, magnesium stearate, sodium lauryl sulfate, sodium stearyl fumarate, zinc stearate, stearic acid or hydrogenated vegetable oil, gum arabica, magnesia, glucose, fats, waxes, natural or hardened oils, water, physiological sodium chloride solution or alcohols, for example, ethanol, propanol or glycerol, sugar solutions, such as glucose solutions or ol solutions and the like or a mixture of the various excipients.

In yet another aspect, the active compounds of the invention may be formulated in the form of pills, tablets, coated s, capsules, powder, granules, pellets, patches, implants, films, s, semi—solids, gels, aerosols, emulsions, elixirs and the like. Such pharmaceutical compositions and processes for preparing same are well known in the art.

In yet another aspect, the pharmaceutical composition of the instant invention contains 1 to 90 %, 5 to 75 % and 10 to 60 % by weight of the compounds of the instant invention or pharmaceutically acceptable salt thereof. The amount of the active compounds or its pharmaceutically acceptable salt in the ceutical composition(s) can range from about 1 mg to about 500 mg or from about 5 mg to about 400 mg or from about 5 mg to about 250 mg or from about 7 mg to about 150 mg or in any range falling within the broader range of 1 mg to 500 mg.

The dose of the active nds can vary depending on factors such as age and weight of patient, nature and ty of the disease to be treated and such other factors.

Therefore, any reference regarding pharmacologically effective amount of the compounds of general formula (I), stereoisomers and pharmaceutically acceptable salts thereof refers to the aforementioned s.

ABBREVATIONS: The following abbreviations are used : 5—HT : 5—Hydroxytryptamine —HT6 : oxytryptamine 6 -HT2A : 5—Hydroxytryptamine 2A ACN : Acetonitrile A1C13 : Aluminum chloride AUC Area under the curve Cmax Maximum concentration CSF Cerebrospinal fluid CHC13 Chloroform CDC13 Deuterated form CSzCO3 Cesium carbonate CD3OD Deuterated methanol DCM Dichloromethane DEA lamine DMF N,N—Dimethylformamide DMSO Dimethyl ide EDC Ethylene dichloride EDTA Ethylenediaminetetraacetic acid Fe Iron g Grams Water Hydrochloric acid Isopropyl alcohol Binding constant Inhibitory constant LC—MS/MS Liquid chromatography—Mass spectrometry/ Mass spectrometry MeOH Methanol NaBH4 Sodium borohydride Nal Sodium iodide NaIO4 Sodium periodate NaHC03 Sodium bicarbonate NiCl Nickel chloride NazSO4 Sodium sulphate NaBH(OAc)3 : Sodium triacetoxyborohydride NH3 a NMDA N-methyl-D-aspartate p.0. Per oral RT Retention Time ROA Route of Administration THF : Tetrahydrofuran m—CPBA : meta—chloro perbenzoic acid NaBH(OAc)3 ; Sodium triacetoxyborohydride h : Hour (s) i. v. : Intravenous NOAEL : No Observed Adverse Effect Level ng : am mg : Milligram s.c. : Sub cutaneous T1/2 : Half—life time EXAMPLES The compounds of the t invention were ed according to the following mental procedures, using appropriate materials and conditions. The following examples are ed by way of illustration only but not to limit the scope of present invention.

Intermediate 1: 2-Nitr0(phenylsulfanyl) phenol OUMS OH CSzCO3 (78 g, 0.24 mole) was added in portions to a stirred solution of 5 —fluoro—2— nitro phenol (31.4 g, 0.2 mole) and thiophenol (24.2 g, 0.22 mole) in DMF (600 mL) at 25 — 35°C. The ing mass was stirred for 1 hour at room temperature, poured on to cold water (1000 mL) during which solids precipitated. These solids were filtered and dissolved in CHC13 (1000 mL). The organic layer was washed with brine (250 mL), dried over anhydrous NaZSO4, filtered and concentrated on rotavap to obtain crude mass which was purified by column chromatography using ethyl acetate: n—hexane (30:70) to obtain 2—nitro— —(phenylsulfanyl)phenol.

Yield: 47.2 g (95 %); 1H — NMR (CDC13, 400 MHZ) 5 ppm: 6.67 — 6.68 (m, 2H), 7.47 — 7.52 (m, 3H), 7.55 — 7.58 (m, 2H), 7.93 — 7.95 (d, J = 9.52 Hz, 1H), 10.7 (s, 1H); Mass (m/z): 247.9 (M+H)+.

Intermediate 2: 5-(Phenylsulf0nyl)nitr0 phenol 0\ ,9 WO 30641 m—CPBA (82.4 g, 0.47 mole) was added in portions to a stirred solution of 2—nitro— —(phenylsulfanyl) phenol (47 g, 0.19 mole) in DCM (1000 mL) at room temperature (exothermic, mild reflux of solvent). The reaction mixture was further stirred for 18 hours at room temperature and poured on to water (500 mL). The organic layer was ted, washed with 10% aqueous NaHC03 solution (250 mL x 2), brine (250 mL), dried over anhydrous , filtered and concentrated on rotavap to obtain 5—phenylsulfonyl—2—nitro phenol.

Yield: 52.2 g (~100 %); 1H - NMR (CDCl3, 400 MHz) 6 ppm: 7.49 — 7.52 (dd, J = 1.52, 8.76 Hz, 1H), 7.55 — 7.58 (m, 2H), 7.63 — 7.67 (m, 1H), 7.76 — 7.76 (d, J = 1.36 Hz, 1H), 7.96 — 7.98 (d, J = 7.48 Hz, 2H), 8.22 — 8.24 (d, J = 8.84 Hz, 1H), 10.58 (s, 1H); Mass (m/z): 278.2 (M-H)+.

Intermediate 3: 2-Amin0(phenylsulf0nyl) phenol E‘s".

: : :OH A sion of 5—(phenylsulfonyl)—2—nitro phenol (52 g, 0.18 mole), Fe (41 g, 0.74 mole) and NH4Cl (49.8 g, 0.93 mole) in H20, l (D.S) and THF (1000 mL:250 mL:250 mL) was refluxed for ~4 h. The reaction mixture was cooled to room temperature and concentrated to obtain a residual mass. Water (500 mL) was added to the above mixture and basified with NaHC03 (pH~9) and the product was extracted with CHC13 (500 mL x 3). The organic ts were combined, washed with brine (250 mL), dried over anhydrous NaZSO4, filtered and concentrated on rotavap to obtain 2—amino—5— (phenylsulfonyl) phenol.

Yield: 41.7 g (~90 %); 1H — NMR (CD3OD, 400 MHz) 5 ppm: 6.71 — 6.71 (m, 1H), 7.13 — 7.22 (m, 2H), 7.51 — 7.53 (m, 3H), 7.83 — 7.85 (m, 2H); Mass (m/z): 250.1 (M+H)+.

Intermediate 4: tert-Butyl 4-(4-phenylsulfonyl-Z-hydroxy phenylamin0) fluoropiperidin-l-carboxylate A suspension of 2—amino—5—(phenylsulfonyl) phenol (40 g, 0.16 mole), tert—butyl 3— fluoro—4—oxo—piperidin—1—carboxylate (41.8 g, .19 mole) in EDC (1000 mL) was refluxed for 4 h to obtain a clear solution. The reaction mixture was cooled to room temperature and NaBH(OAc)3 (102 g, 0.48 mole) was added to above solution in three equal lots, each in 1 h time al. The reaction mixture was stirred for 18 h at room temperature, and again refluxed for 1 h. The on mixture was cooled to room temperature, added water (500 mL), and basified with aq. NH3 solution (pH~9). The organic layer was separated and aqueous layer was extracted with ethyl acetate (500 mL x 3). The organic extracts were combined, washed with brine (250 mL), dried over anhydrous NaZSO4, filtered and concentrated on rotavap to obtain crude mass which was purified by column chromatography using ethyl acetate: n—hexane (30:70) to obtain tert—butyl 4—(4— phenylsulfonyl—2—hydroxy phenylamino)—3—fluoro piperidin—1—carboxylate as a diastereomeric mixture.

Yield: 60.3 g (~83 %); HPLC (55.5% and 40.8%); reomeric pair; Mass (m/z): 449.4 (M-H)+.

Intermediate 5: tert-Butyl henylsulfonyl(2-chlor0eth0xy) phenylamin0] fluoropiperidin-l-carboxylate OSUO%C'NH Potassium ate (73.5 g, 0.53 mole) was added to a stirred mixture of tert—butyl henylsulfonyl—2—hydroxy phenylamino)—3—fluoro piperidin—1—carboxylate (60 g, 0.13 mole), 1—bromo—2—chloroethane and NaI (2 g, 0.013 mole) in acetonitrile (1000 mL). The reaction mixture was refluxed for 5 h, cooled to room temperature, poured on to water (1000 mL) and ted with ethyl acetate (1000 mL x 2). The organic extracts were combined, dried over anhydrous NaZSO4, filtered and concentrated on p to obtain crude mass which was purified by column chromatography. First eluting diastereomer (along with some second eluting isomer) was obtained in ethyl acetate:CHC13 (3:97) and the second eluting diastereomer (along with some first eluting isomer) was obtained in ethyl acetate:CHC13 (5:95 and then ethyl acetate was increased in gradient).

First eluting : Yield: 12.74 g (~18.6 %); HPLC 85.5%; 1H — NMR (CDC13, 400 MHz) 5 ppm: 1.49 (s, 9H), 1.53 — 1.59 (m, 1H), 2.13 — 2.16 (m, 1H), 3.12 — 3.25 (m, 2H), 3.62 — 3.65 (m, 1H), 3.85 — 3.88 (m, 2H), 4.11 — 4.15 (m, 1H), 4.31 — 4.34 (m, 3H), 4.45 — 4.46 (m, 1H), 4.92 — 4.94 (d, J = 7.38 Hz, 1H), 6.74 — 6.76 (d, J = 8.58 Hz, 1H), 7.24 — 7.25 (m, 1H), 7.46 — 7.54 (m, 4H), 7.89 — 7.91 (d, J = 7.26 Hz, 2H); Mass (m/z): 513.6, 515.5 (M+H)+.

Second eluting isomer: Yield: 24.69 g ; HPLC 91.5%; 1H — NMR (CDCl3, 400 MHz) 5 ppm: 1.49 (s, 9H), 1.79 — 1.87 (m, 2H), 2.86 — 3.12 (m, 2H), 3.55 — 3.62 (m, 1H), 3.84 — 3.87 (m, 2H), 4.12 — 4.17 (m, 1H), 4.30 — 4.33 (m, 2H), 4.41 -4.53 (m, 1H), 4.69 — 4.92 (m, 1H), 5.13 — 5.15 (d, J = 9.12 Hz, 1H), 6.59 — 6.61 (d, J = 8.46 Hz, 1H), 7.27 — 7.29 (m, 1H), 7.47 — 7.56 (m, 4H), 7.90 — 7.91 (d, J = 7.1 Hz, 2H); Mass (m/z): 513.4, 515.2 (M+H)+.

Intermediate 6: tert-Butyl 4-(7-phenylsulf0nyl-2,3-dihydr0benz0[1,4]0xazinyl) fluoropiperidin-l-carboxylate Sodium e (2.6 g, 0.064 mole, 60% dispersion in mineral oil) was added in portions to a stirred mixture of tert—butyl henylsulfonyl—2—(2—chloroethoxy) phenylamino]—3—fluoro piperidin—l—carboxylate (second eluting isomer, 22 g, 0.04 mole) and Nal (0.32 g, 0.002 mole) in DMF (220 mL) at room temperature and stirred for 18 hours. The reaction mixture was then poured on to water (500 mL) and extracted with CHC13 (300 mL x 3). The organic extracts were combined, washed with brine (50 mL), dried over anhydrous , filtered and concentrated on rotavap to obtain tert—butyl 4— (7—phenylsulfonyl—2,3—dihydro benzo[1,4]oxazin—4—yl)—3—fluoro piperidin—l—carboxylate as off white solids. These solids were triturated with n—hexane (100 mL x 3) and the product was dried in vacuum on rotavap.

Yield: 18.3 g (~89 %); HPLC (90.1%); 1H — NMR (CDC13, 400 MHz) 5 ppm: 1.47 (s, 9H), 1.64 — 1.65 (m, 1H), 2.21 — 2.31 (m, 1H), 2.82 — 3.05 (m, 2H), 3.37 — 3.47 (m, 1H), 3.54 — 3.57 (m, 1H), 3.78 — 3.89 (m, 1H), 4.12 — 4.18 (m, 2H), 4.42 — 4.59 (m, 2H), 4.78 — 4.90 (m, 1H), 6.58 — 6.60 (d, J = 8.74 Hz,1H), 7.31 —7.31 (d, J = 1.94 Hz, 1H), 7.41 — 7.51 (m, 4H), 7.89 — 7.90 (d, J = 7.21 Hz, 2H); Mass (m/z): 477.2 (M+H)+.

Intermediate 7: Chiral separation of utyl 4-(7-phenylsulf0nyl-2,3- dihydrobenzo[1,4]oxazinyl)—3-flu0r0piperidin-l-carboxylate Intermediate 6 (having 10% minor fraction and 90% major fraction as per HPLC) was separated by Chiral column Chromatography to Intermediate 7 as four separate peaks, using the method given below.

Method: Column ID: CHIRALPAK IC, Mobile Phase: hyl acetate (75:25), Flow rate: 1 mL/min, Temp: 25 OC, Wavelength: 320 nM.

Intermediate 7 (Peak I): Chiral HPLC 99.9%, (RT: 8.6 min); 1H — NMR (CDC13, 400 MHz) 6 ppm: 1.47 (s, 9H), 1.61 — 1.68 (m, 2H), 1.82 — 1.86 (m, 1H), 2.78 — 2.84 (m, 2H), 3.34 — 3.44 (m, 2H), 3.88 — 3.91 (m, 1H), 4.16 — 4.22 (m, 3H), 4.57 — 4.62 (m, 1H), 6.77 — 6.79 (d, J = 8.76 Hz, 1H), 7.31 — 7.31 (d, J = 1.72 Hz, 1H), 7.42 — 7.52 (m, 4H), 7.88 — 7.90 (d, J = 7.48 Hz, 2H); Mass (m/z): 477.3 (M+H)+.

Intermediate 7 (Peak II): Chiral HPLC 99.8%, (RT: 10.7 min); 1H — NMR (CDC13, 400 MHz) 6 ppm: 1.47 (s, 9H), 1.61 — 1.68 (m, 2H), 1.82 — 1.86 (m, 1H), 2.78 — 2.84 (m, 2H), 3.34 — 3.44 (m, 2H), 3.88 — 3.91 (m, 1H), 4.16 — 4.22 (m, 3H), 4.57 — 4.62 (m, 1H), 6.77 — 6.79 (d, J = 8.76 Hz, 1H), 7.31 — 7.31 (d, J = 1.72 Hz, 1H), 7.42 — 7.52 (m, 4H), 7.88 — 7.90 (d, J = 7.48 Hz, 2H); Mass (m/z): 477.5 .

Intermediate 7 (Peak III): Chiral HPLC 99.9%, (RT: 12.2 min); 1H — NMR (CDC13, 400 MHz) 6 ppm: 1.47 (s, 9H), 1.62 — 1.64 (m, 1H), 2.24 — 2.28 (m, 1H), 2.84 — 3.01 (m, 2H), 3.42 — 3.47 (m, 1H), 3.54 — 3.58 (m, 1H), 3.76 — 3.87 (m, 1H), 4.14 — 4.19 (m, 2H), 4.43 — 4.50 (m, 2H), 4.78 — 4.91 (m, 1H), 6.58 — 6.60 (d, J = 8.74 Hz, 1H),7.31— 7.32 (d, J = 1.70 Hz, 1H), 7.41 — 7.53 (m, 4H), 7.89 7.91 (d, J = 7.31 Hz, 2H); Mass (m/z): 477.1 (M+H)+.

Intermediate 7 (Peak IV): Chiral HPLC 99.7%, (RT: 17.8 min); 1H — NMR (CDC13, 400 MHz) 6 ppm: 1.47 (s, 9H), 1.62 — 1.64 (m, 1H), 2.24 — 2.28 (m, 1H), 2.84 — 3.01 (m, 2H), 3.42 — 3.47 (m, 1H), 3.54 — 3.58 (m, 1H), 3.76 — 3.87 (m, 1H), 4.14 — 4.19 (m, 2H), 4.43 — 4.50 (m, 2H), 4.78 — 4.91 (m, 1H), 6.58 — 6.60 (d, J = 8.74 Hz, 1H),7.31— 7.32 (d, J 21.70 Hz, 1H),7.41— 7.53 (m, 4H), 7.89 7.91 (d, J = 7.31 Hz, 2H); Mass (m/z): 477.1 (M+H)+.

Example 1: 7-Phenylsulf0nyl(3-flu0r0piperidinyl)-3,4-dihydr0-2H-benz0[1,4]oxazine hydrochloride (Peak III) Methanolic HCl (16% w/V solution, 1.3 mL, 0.005 mole) was added to a stirred suspension of tert—butyl (4—(7—phenylsulfonyl—2,3—dihydro benzo[1,4]oxazin—4—yl)—3—fluoro din—1—carboxylate (Intermediate 7 (Peak III), 0.5 g, 0.001 mole) in ol (10 mL) and the resuling mixture was refluxed for ~ 4 h to obtain a clear solution. The reaction mixture was cooled to room temperature and concentrated invacuum on rotavapor to obtain crystalline solid.

Yield: 0.41 g (95 %); 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.81 — 1.84 (m, 1H), 2.24 — 2.32 (m, 1H), 3.10 — 3.16 (m, 1H), 3.36 — 3.41 (m, 2H), 3.46 — 3.53 (m, 3H), 4.09 — 4.18 (m, 2H), 4.32 — 4.38 (m, 1H), 5.05 — 5.17 (d, J = 47.8 Hz, 1H), 7.04 — 7.06 (d, J = 8.89 Hz, 1H), 7.17 — 7.18 (d, J = 2.05 Hz, 1H), 7.33 — 7.36 (m, 1H), 7.55 — 7.65 (m, 3H), 7.88 — 7.89 (d, J = 7.4 Hz, 2H), 8.73 (bs, 1H), 9.52 (bs, 1H); Mass (m/z): 377.0 (M+H)+; HPLC (% purity): 99.93.

Example 2: 7-Phenylsulfonyl(3-fluoropiperidinyl)-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride (Peak I) The title compound was prepared from tert—butyl 4—(7—phenylsulfonyl—2,3— dihydrobenzo[1,4]oxazin—4—yl)—3—fluoropiperidin—1—carboxylate (Intermediate 7 (Peak 1)) by ing the experimental procedure of Example 1. 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.87 — 1.90 (m, 1H), 1.97 — 2.09 (m, 1H), 3.04 — 3.10 (m, 2H), 3.37 — 3.39 (m, 3H), 3.63 — 3.66 (m, 1H), 4.14 — 4.18 (m, 2H), 4.46 — 4.48 (m, 1H), 5.00 — 5.15 (m, 1H), 7.07 — 7.11 (d, J = 8.84 Hz, 1H), 7.15 — 7.16 (d, J = 1.69 Hz, 1H), 7.34 — 7.36 (dd, J = 1.27, 8.7 Hz, 1H), 7.55 — 7.65 (m, 3H), 7.87 — 7.89 (d, J = 7.38 Hz, 2H), 8.56 (bs, 1H), 9.38 (bs, 1H); Mass (m/z): 377.2 (M+H)+; HPLC (% ): 99.96.

Example 3: ylsulfonyl(3-fluoropiperidinyl)-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride (Peak II) The title compound was prepared from tert—butyl 4—(7—phenylsulfonyl—2,3— dihydrobenzo[1,4]oxazin—4—yl)—3—fluoropiperidin—1—carboxylate (Intermediate 7 (Peak 11)) by following the experimental procedure of Example 1. 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.89 — 1.90 (m, 1H), 1.99 — 2.02 (m, 1H), 3.07 — 3.16 (m, 2H), 3.39 — 3.40 (m, 3H), 3.64 — 3.66 (m, 1H), 4.13 — 4.19 (m, 2H), 4.46 — 4.48 (m, 1H), 5.13 — 5.15 (m, 1H), 7.09 — 7.11 (d, J = 8.91 Hz, 1H), 7.15 — 7.16 (d, J = 2.61 Hz, 1H), 7.34 — 7.36 (dd, J = 1.76, 8.75 Hz, 1H), 7.55 — 7.65 (m, 3H), 7.87 — 7.89 (d, J = 7.4 Hz, 2H), 8.53 (bs, 1H), 9.34 (bs, 1H); Mass (m/z): 377.2 (M+H)+; HPLC (% purity): 94.00.

Example 4: 7-Phenylsulfonyl(3-fluoropiperidinyl)-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride (Peak IV) The title compound was prepared from tert—butyl 4—(7—pheny1su1fony1—2,3— dihydrobenzo[1,4]oxazin—4—y1)—3—fluoropiperidin—1—carboxy1ate (Intermediate 7 (Peak IV)) by following the experimental procedure of Example 1. 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.81 — 1.84 (m, 1H), 2.27 — 2.34 (m, 1H), 3.12 — 3.15 (m, 1H), 3.37 — 3.52 (m, 5H), 4.10 — 4.16 (m, 2H), 4.31 — 4.37 (m, 1H), 5.05 — 5.17 (d, J = 47.8 Hz, 1H), 7.05 — 7.07 (d, J = 8.86 Hz, 1H), 7.17 — 7.17 (d, J = 1.99 Hz, 1H), 7.33 — 7.35 (dd, J = 1.87, 8.66 Hz, 1H), 7.56 — 7.63 (m, 3H), 7.87 — 7.89 (d, J = 7.38 Hz, 2H), 8.68 (bs, 1H), 9.66 (bs, 1H); Mass (m/z): 377.2 (M+H)+; HPLC (% purity): 99.63.

Examples 5 to 8: The nds of examples 5 to 8 were prepared by following the experimental procedures as described in the examples 1 to 4, with some non—critical variations using riate ediates.

Example 5: 7-(3-Fluorophenylsulfonyl)(3-fluoropiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (Peak 1) O"3"0 : :N01 F F 1H — NMR d6, 400 MHz) 6 ppm: 1.90 — 2.01 (m, 2H), 3.05 — 3.15 (m, 3H), 3.34 — 3.39 (m, 2H), 3.64 — 3.67 (m, 1H), 4.12 — 4.19 (m, 2H), 4.45 — 4.49 (m, 1H), 4.94 — 5.13 (m, 1H), 7.08 — 7.10 (d, J = 8.90 Hz, 1H), 7.20 — 7.21 (d, J = 2.09 Hz, 1H), 7.37 — 7.40 (dd, J = 2.04, 8.75 Hz, 1H), 7.49 — 7.51 (m, 1H), 7.61 — 7.65 (m, 1H), 7.71 — 7.75 (m, 2H), 9.09 (bs, 1H), 9.29 (bs, 1H); Mass (m/z): 395.2 (M+H)+; HPLC (% purity): 99.8.

Example 6: WO 30641 7-(3-Fluorophenylsulfonyl)(3-fluoropiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (Peak 11) 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.90 — 2.01 (m, 2H), 3.06 — 3.15 (m, 3H), 3.35 — 3.39 (m, 2H), 3.64 — 3.67 (m, 1H), 4.12 — 4.19 (m, 2H), 4.45 — 4.50 (m, 1H), 4.94 — 5.10 (m, 1H), 7.08 — 7.10 (d, J = 9.8 Hz, 1H), 7.20 — 7.21 (d, J = 2.02 Hz, 1H), 7.37 — 7.40 (dd, J = 2.02, 8.74 Hz, 1H), 7.46 — 7.51 (m, 1H), 7.59 — 7.64 (m, 1H), 7.71 — 7.75 (m, 2H), 9.09 (bs, 1H), 9.29 (bs, 1H); Mass (m/z):395.2 (M+H)+; HPLC (% purity): 99.8.

Example 7: 7-(3-Fluorophenylsulfonyl)(3-fluoropiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (Peak 111) 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.81 — 1.84 (m, 1H), 2.17 — 2.31 (m, 1H), 3.12 — 3.15 (m, 1H), 3.31 — 3.36 (m, 2H), 3.46 — 3.57 (m, 3H), 4.11 — 4.17 (m, 2H), 4.29 — 4.40 (m, 1H), 5.50 — 5.17 (d, J = 47.68 Hz, 1H), 7.02 — 7.04 (d, J = 8.87 Hz, 1H), 7.22 — 7.22 (d, J = 1.69 Hz, 1H), 7.37 — 7.39 (dd, J = 1.52, 8.68 Hz, 1H), 7.47 — 7.51 (m, 1H), 7.60 — 7.65 (m, 1H), 7.72 — 7.76 (m, 2H), 8.45 — 8.68 (bs, 1H), 9.36 (bs, 1H); Mass (m/z): 395.2 (M+H)+; HPLC (% purity): 99.39.

Example 8: 7-(3-Fluorophenylsulfonyl)(3-fluoropiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (Peak IV) 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.81— 1.84 (m, 1H), 2.25 — 2.31 (m, 1H), 3.11 — 3.13 (m, 1H), 3.32 — 3.36 (m, 2H), 3.46 — 3.57 (m, 3H), 4.13 — 4.14 (m, 2H), 4.28 — 4.40 (m, 1H), 5.05 — 5.17 (d, J = 47.71 Hz, 1H), 7.01 — 7.03 (d, J = 8.74 Hz, 1H). 7.22 — 7.22 (d, J = 1.65 Hz, 1H), 7.37 — 7.39 (m, 1H), 7.47 — 7.51 (m, 1H), 7.59 — 7.65 (m, 1H), 7.72 — 7.76 (m, 2H), 8.66 (bs, 1H), 9.24 (bs, 1H); Mass (m/z): 395.2 (M+H)+; HPLC (% purity): 98.78.

Racemic- 4-(3-Fluoropiperidinyl)(pyridinesulfonyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride Step-1: 2-Nitro(pyridinsulfonyl)phenol "s" OH / N UN, NaIO4 (29 g, 0.13 mole) was added to a stirred mixture of 2—nitro—5—(pyridin—2— anyl) phenol (6.8 g, 0.027 mole) in IPA:HZO (100 mL:200 mL) and the reaction mixture was refluxed for 24 h. The reaction mixture was then cooled to room temperature, extracted using DCM (150 mL x 3). The organic extracts were combined, dried over anhydrous NaZSO4, filtered and concentrated on rotavap to obtain crude mass which was purified by column chromatography using ethyl acetate: n—hexane (30:70) to obtain o— 5—(pyridin—2—sulfonyl)—phenol.

Yield: 6.2 g (81%); 1H — NMR (DMSO—d6, 400 MHz) 5 ppm: 7.45 — 7.48 (m, 1H), 7.69 — 7.75 (m, 2H), 8.02 — 8.04 (d, J = 8.56 Hz, 1H), 8.16 — 8.28 (m, 2H), 8.72 — 8.73 (d, J = 4.2 Hz, 1H), 11.96 (bs, 1H); Mass (m/z): 279.2 .

Racemic- 4-(3-Fluoropiperidinyl)(pyridinesulfonyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride The title compound was synthesized by following the experimental procedures as described in ediates 4 to 6, with some non—critical variations using 2—nitro—5— in—2—sulfonyl) phenol (obtained in above step) and appropriate intermediates. 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.82 — 1.85 (m, 1H), 2.24 — 2.32 (m, 1H), 3.11 — 3.15 (m, 2H), 3.47 — 3.53 (m, 4H), 4.09 — 4.18 (m, 2H), 4.30 — 4.39 (m, 1H), 5.06 — 5.18 (d, J = 47.81 Hz, 1H), 7.04 — 7.07 (d, J = 8.86 Hz, 1H), 7.17 — 7.17 (d, J = 2 Hz, 1H), 7.33 — 7.36 (dd, J = 1.84, 8.68 Hz, 1H), 7.61— 7.64 (m, 1H), 8.06 — 8.11 (m, 2H), 8.66 — 8.70 (m, 2H), 9.49 (bs, 1H); Mass (m/z): 378.2 (M+H)+; HPLC (% purity): 97.54.

Example 10: Racemic(3-Fluoropiperidinyl)(pyridinesulfonyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride Step-1: 2-Nitro(pyridinsulfonyl)phenol \ °§UOH The title compound was synthesized from 2—nitro—5—(pyridin—4—ylsulfanyl)phenol following the procedure as described in step 1 of e 9.

Yield: 1.4 g (95%); 1H - NMR d6, 400 MHz) 6 ppm: 7.53 — 7.55 (d, J = 8.04 Hz, 1H), 7.66 — 7.67 (m, 1H), 7.91 — 7.93 (m, 2H), 8.05 — 8.07 (d, J = 8.16 Hz, 1H), 8.90 — 8.92 (m, 2H), 12.03 (bs, 1H); Mass (m/z): 279.2 .

Racemic(3-Fluoropiperidinyl)(pyridinesulfonyl)-3,4-dihydro-2H- 1,4]oxazine hydrochloride The title compound was synthesized by following the experimental procedures as described in intermediates 4 to 6, with some non—critical variations using 2—nitro—5— (pyridin—4—sulfonyl)phenol (obtained in above step) and appropriate intermediates.

Mass (m/z): 378.4 (M+H)+.

Example 11: 7-Phenylsulfonyl(3-fluoromethylpiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (First eluting isomer) 0\\S//0 O (IN)O H HC1 This e was prepared by following the experimental procedures as described in intermediate 6, with some non—critical variations using appropriate intermediates. 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.46 — 1.52 (d, J = 24.5 Hz, 3H), 2.02 — 2.05 (m, 2H), 3.07 — 3.08 (m, 1H), 3.29 — 3.31 (m, 2H), 3.39 — 3.47 (m, 3H), 4.12 — 4.18 (m, 2H), 4.39 — 4.45 (m, 1H), 7.07 — 7.09 (d, J = 8.7 Hz, 1H), 7.13 (d, J = 1.81 Hz, 1H), 7.30 — 7.33 (dd, J = 1.5, 8.7 Hz, 1H), 7.54 — 7.63 (m, 3H), 7.85 — 7.87 (d, J = 7.49 Hz, 2H), 8.97 (bs, 1H), 9.63 (bs, 1H); Mass (m/z): 391.3 ; HPLC (% purity): 99.79.

Example 12: 7-Phenylsulfonyl(3-fluoromethylpiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride (Second eluting isomer) 0\\S//0 O (IN)O H HC1 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.26 — 1.32 (d, J = 22.3 Hz, 3H), 1.76 — 1.79 (m, 1H), 2.17 — 2.26 (m, 1H), 3.05 — 3.10 (m, 1H), 3.32 — 3.49 (m, 5H), 4.08 — 4.20 (m, 2H), 4.29 — 4.39 (m, 1H), 7.12 — 7.15 (, 2H), 7.31 — 7.33 (dd, J = 1.53, 8.67 Hz, 1H), 7.54 — 7.64 (m, 3H), 7.87 — 7.89 (d, J = 7.44 Hz, 2H), 8.66 (bs, 1H), 9.53 (bs, 1H); Mass (m/z): 391.3 ; HPLC (% purity): 99.07.

Example 13: Racemic- ylsulfonyl(3-fluoropiperidinyl)-3,4-dihydro-2H- benzo[1,4]oxazine hydrochloride 08¢ N o o KTF HCI Step-1: 4-Phenylsulfonylnitro phenol ©g8%©:N02OH A1C13 (7.2 g, 0.53 mole) was added to ophenol (5 g, 0.035 mole) at room temperature under mechanical stirring, maintained for ~15 min followed by the addition of benzenesulfonyl chloride (7.6 g, 0.043 mole). The reaction mixture was heated to 140 °C and maintained for 3 h to obtain a thick dark al. The reaction mixture was cooled to room temperature, added to cold water (250 mL), extracted with ethyl acetate (100 mL x 3). The organic extracts were combined, dried over anhydrous NaZSO4, filtered and concentrated on rotavap to obtain crude mass which was purified by column chromatography using ethyl acetate: ne (20:80) to obtain 4—phenylsulfonyl—2—nitro phenol.

Yield: 4.3 g (43 %); 1H - NMR (DMSO-d6, 400 MHz) 6 ppm: 7.28 — 7.30 (d, J = 8.9 Hz, 1H), 7.59 — 7.63 (m, 2H), 7.67 — 7.71 (m, 1H), 7.95 — 7.97 (d, J = 8.81 Hz, 2H), 8.02 — 8.04 (dd, J = 2.18, 8.95 Hz, 1H), 8.40 — 8.41 (d, J = 2.14 Hz, 1H).

Step-2: 2-Amin0phenylsulf0nyl phenol Yield: 3.4 g (89 %); 1H - NMR (DMSO-d6, 400 MHz) 6 ppm: 5.03 (bs, 2H), 6.74 — 6.76 (d, J = 8.2 Hz, 1H), 6.98 — 7.00 (dd, J = 2.12, 8.16 Hz, 1H), 7.07 — 7.08 (d, J = 2.08 Hz, 1H), 7.54 — 7.63 (m, 3H), 7.79 — 7.81 (d, J = 7.2 Hz, 2H), 10.2 (bs, 1H); Mass (m/z): 248.4 (M- Step-3: tert-Butyl henylsulfonyl-Z-hydroxy amin0)flu0r0 piperidin-l- ylate ©3112: The title compound was synthesized from 2—amino—4—phenylsulfonyl phenol following the procedure as described in Intermediate 4. This compound was isolated as a diastereomeric mixture.

Yield: 2.4 g (85 %); Mass (m/z): 449.1 (M—H)+.

Step-4: tert-Butyl 4-[5-phenylsulfonyl(2-chloroethoxy)phenylamino]flu0r0 piperidin-l-carboxylate S NH ’/ \\ 0 0 6F The title compound was synthesized from tert—butyl 4—(5—phenylsulfonyl—2— hydroxy—phenylamino)—3—fluoropiperidine—1—carboxylate following the procedure as described in ediate 5. This compound was isolated as a reomeric mixture.

Yield: 1.87 g (68 %); HPLC (40.3%, 53.7%); Mass (m/z): 513.2 (M+H)+.

Step-5: tert-Butyl 4-(6-phenylsulf0nyl-3,4-dihydr0 benz0[1,4]0xazinyl)flu0r0 piperidin-l-carboxylate The title compound was synthesized from tert—butyl 4—[5—phenylsulfonyl—2—(2— chloroethoxy) phenylamino]—3—fluoro piperidin—1—carboxylate following the procedure as described in Intermediate 6. This compound was isolated as a reomeric mixture.

Yield: 0.39 g (23 %); HPLC (40.3%, 53.7%); Mass (m/z): 477.2 (M+H)+.

Step-6: RacemicPhenylsulf0nyl(3-flu0r0piperidinyl)-3,4-dihydr0-2H- 1,4]0xazine hydrochloride The title compound was synthesized from utyl 4—(6—phenylsulfonyl—3,4— dihydro—benzo[1,4]oxazin—4—yl)—3—fluoropiperidin—1—carboxylate following the procedure as described in example 1. This compound was isolated as a diastereomeric mixture.

Yield: 0.62 g (87 %); HPLC (47.08%, 47.30%); Mass (m/z): 377.2 (M+H)+. e 14 to 17: The Examples 14 to 17 were obtained by chiral separation of 6— Phenylsulfonyl—4—(3—fluoro piperidin—4—yl)—3 ,4—dihydro—2H—benzo[1,4]oxazine hydrochloride (Example 13) in the form of free base using the method given below.

Method: Column ID: 250 x 4.6 mm, 5 um, PAK IC; Mobile Phase: 0.1% diethyl amine in methanol; Flow rate: 1 mL/min; Temp: 25 OC; Wavelength: 243 nM.

Example 14: 6-Phenylsulf0nyl(3-fluoropiperidinyl)-3,4-dihydr0-2H-benz0[1,4] 0xazine (Peak Chiral HPLC 93.5%, (RT: 5.2 min), Mass (m/z): 377.1 .

Example 15: 6-Phenylsulf0nyl(3-fluoropiperidinyl)-3,4-dihydr0-2H-benz0[1,4] 0xazine (Peak Chiral HPLC 98.1 %, (RT: 5.9 min), Mass (m/z): 377.5 .

Example 16: 6-Phenylsulf0nyl(3-fluoropiperidinyl)-3,4-dihydr0-2H-benz0[1,4] 0xazine (Peak Chiral HPLC 96.50%, (RT: 8.1 min), Mass (m/z): 377.1 (M+H)+.

Example 17: 6-Phenylsulf0nyl(3-fluoropiperidinyl)-3,4-dihydr0-2H-benz0[1,4] 0xazine (Peak Chiral HPLC 98.1 %, (RT: 15.1 min), Mass (m/z): 377.0 (M+H)+.

Example 18: 7-Phenylsulf0nyl[3-flu0r0(2-fluoroethyl)piperidinyl]-3,4-dihydr0-2H- benz0[1,4]0xazine (Peak III) CSzCO3 (0.097 g, 0.0003 mole) was added to a stirred solution of 7—phenylsulfonyl— 4—(3—fluoropiperidin—4—yl)—3,4—dihydro—2H—benzo[1,4]oxazine hydrochloride (0.04 g, 0.00009 mole, Example 1) and o—2—fluoroethane (0.037 g, 0.0003 mole) in acetonitrile (5 mL) and refluxed for 8 h. The reaction mixture was then cooled to room temperature, poured on to water (5 mL) and ted with ethyl acetate (15 mL x 3). The organic extracts were combined, dried over anhydrous NaZSO4, filtered and concentrated on p to obtain crude mass which was ed by column chromatography using ethyl acetate: methanol (2:98) to the title compound.

Yield: 0.028 g (70%), 1H — NMR (DMSO-d6, 400 MHz) 6 ppm: 1.26 — 1.32 (d, J = 22.3 Hz, 3H), 1.76 — 1.79 (m, 1H), 2.17 — 2.26 (m, 1H), 3.05 — 3.10 (m, 1H), 3.32 — 3.49 (m, 5H), 4.08 — 4.20 (m, 2H), 4.29 — 4.39 (m, 1H), 7.12 — 7.15 (, 2H), 7.31 — 7.33 (dd, J = 1.53, 8.67 Hz, 1H), 7.54 — 7.64 (m, 3H), 7.87 — 7.89 (d, J = 7.44 Hz, 2H), 8.66 (bs, 1H), 9.53 (bs, 1H); Mass (m/z): 423.1 (M+H)+; HPLC (% purity): 99.07.

Example 19: 7-Phenylsulf0nyl[3-flu0r0(2-fluoroethyl)piperidinyl]-3,4-dihydr0-2H- 1,4]0xazine (Peak IV) The title compound was synthesized from 7—phenylsulfonyl—4—(3—fluoropiperidin—4— yl)—3,4—dihydro—2H—benzo[1,4]oxazine hydrochloride (Example 4) following the procedure as described in Example 18.

Yield: 0.031 g (75 %); 1H — NMR (CDC13, 400 MHz) 6 ppm: 1.62 — 1.68 (m, 1H), 2.40 — 2.44 (m, 2H), 2.78 — 2.86 (m, 2H), 3.16 — 3.18 (m, 1H), 3.30 — 3.33 (m, 1H), 3.45 — 3.48 (m, 2H), 3.59 — 3.63 (m, 1H), 3.64 — 3.69 (m, 1H), 4.14 — 4.17 (m, 2H), 4.53 — 4.57 (m, 1H), 4.65 — 4.69 (m, 1H), 4.82 — 4.94 (d, J = 49.35 Hz, 1H), 6.56 — 6.58 (d, J = 8.72 Hz, 1H), 7.29 — 7.30 (m, 1H), 7.11 — 7.52 (m, 4H), 7.89 — 7.91 (d, J = 7.27 Hz, 2H); Mass (m/z): 423.4 (M+H)+; HPLC (% purity): 98.71. e 20: Determination of Kb for 5-HT6 Receptor: A stable CHO cell line expressing recombinant human 5—HT6 receptor and pCRE— Luc reporter system was used for cell based assay. The assay offers a non—radioactive based approach to determine binding of a compound to GPCRs. In this specific assay, the level of intracellular cyclic AMP which is modulated by activation or inhibition of the receptor is measured. The recombinant cells harbor luciferase reporter gene under the control of CAMP response element. The above cells were plated in 96 well clear bottom white plates at a density of 5 x 104 cells/well using Hams F12 medium containing 10% fetal bovine serum (FBS) and incubated overnight at 37°C and 5 % C02 followed by serum starvation for 18 — 20 hrs. Increasing concentrations of test compounds were added along with 10 uM serotonin in Opti—MEM to the cells. The incubation was continued at 37°C in C02 tor for 4 hours. After 4 hours cells were lysed using lysis buffer and luciferase assay buffer was added to each well and counts per second were recorded using luminescence counter. From counts per second (CPS) obtained, percent binding was calculated for each well by taking 10 uM 5—HT as 100 % bound and vehicle as 0 % bound.

The t bound values were plotted against compound concentrations and data were analyzed using a ear, iterative curve— fitting computer program of Graph pad Prism 4 software. The Kb values were calculated using concentration of the agonist used in the assay.

References: Br. J. Pharmacol. 2006, 148, 1133—1143.

Mal. Brain Res. 2001, 90, 110—117. ination of 5-HT2A Binding: Membrane preparation from recombinant human 5—HT2A cell line (Cat no.ES—313— M400UA) and radio ligand Ketanserin Hydrochloride, [Ethylene—3H]—(R—41468) (Cat no.

NET791250UC) were purchased from Perkin Elmer. All other ts used in buffer preparation were purchased from Sigma. The final ligand concentration was 1.75 nM; non— specific determinant was 1—NP [10 uM] and 5—HT2A membrane protein (5 ug/ well). 1—NP was used as a positive control. Reactions were carried out in 67 mM Tris pH 7.6 containing 0.5 mM EDTA buffer for 60 minutes at 25 0C. Reaction was stopped by rapid filtration followed by six washes of the binding mixture using 96 well harvest plate (Millipore Cat no. MSFBNXB50) pre coated with 0.33% polyethyleneimine. The plate was dried and the bound radioactivity collected on the s was determined by scintillation ng using eta TriLux. Radio ligand binding in the presence of non—labeled compound was expressed as a percent of the total binding and d against the log tration of the compound. K values were determined using a nonlinear, iterative curve—fitting computer program of Graph pad Prism 4 software.

J. Pharmacol. Exp. Ther. 1993, 265, 1272—1279.

Table l: In-vitro data —19-73 Comparator 0.1 902 Example Conclusion: Above data clearly shows that the nds of instant invention show high selectivity over 5—HT2A receptor as compared to the comparator example of US7378415.

Comparative Example: 7-Phenylsulfonyl(piperidinyl)-3,4-dihydro-2H-benzo[1,4]oxazine.

The comparative example is synthesized as per the US7378415 procedure. e 21: Rodent Pharmacokinetic Study Male Wistar rats (260 i 50 grams) were used as experimental animals. Animals were housed individually in polypropylene cage. Two days prior to study, male Wistar rats were anesthetized with isoflurane for surgical placement of jugular vein catheter. Rats were randomly divided for oral (3 mg/kg) and intravenous (1 mg/kg) dosing (n = 3/group) and fasted overnight before oral dosing (p.0.). However, rats allocated to intravenous dosing food and water was provided ad libitum.

At termined point, blood was collected h jugular vein and replenished with an equivalent volume of normal saline. Collected blood was transferred into a labeled eppendorf tube containing 10 uL of heparin as an agulant. lly blood samples were ted at following time points: 0.08, 0.25, 0.5, l, 2, 4, 6, 8, and 24 hours post dose. Blood was centrifuged at 4000 rpm for 10 minutes. Plasma was separated and stored frozen at —80 °C until analysis. The concentrations of the test compounds were quantified in plasma by qualified LC—MS/MS method using suitable tion technique. The test compounds were quantified in the calibration range around l—lOOO ng/mL in plasma. Study samples were analyzed using calibration samples in the batch and quality control s spread across the batch.

Pharmacokinetic parameters Cum, AUCt, Tm, Clearance and Bioavailability (F) were calculated by non—compartmental model using standard non—compartmental model by using Phoenix WinNonlin 6.2 or 6.4 version Software e.

Table 2: Pharmacokinetic profile Example AUC0_t Clearance ROA (ng/mL No. (ng.hr/mL) (mL/min/kg) 84 i 141004 + 15 (gavage) intravenous (bolus) Example 22: Rodent Brain Penetration Study Male Wistar rats (260 i 40 grams) were used as experimental animals. Three animals were housed in each cage. Animals were given water and food ad libitum throughout the experiment and maintained on a 12 hours light/dark cycle.

Brain penetration was determined in discrete manner in rats. One day prior to dosing day, male Wistar rats were acclimatized and randomly grouped ing to their weight. At each time point (0.50, l and 2 hours) n = 3 animals were used.

The test nds were suitably preformulated and administered orally at (free base equivalent) 3 mg/kg. Blood samples were collected via cardiac puncture by using isoflurane anesthesia. The animals were sacrificed to collect brain tissue. Plasma was separated and brain samples were homogenized and stored frozen at —20 °C until analysis.

The concentrations of the test nds in plasma and brain were determined using LC— MS/MS method.

The test compounds were quantified in plasma and brain homogenate by qualified MS method using suitable tion technique. The test compounds were quantified in the calibration range of l—lOOO ng/mL in plasma and brain homogenate.

Study samples were analyzed using calibration samples in the batch and quality control samples spread across the batch. Extent of brain—plasma ratio (Cb/Cp) was calculated.

Table 3: Blood Brain ation data Single dose rat brain penetration Example No.

(Cb/Cp) at 3 mg/kg, p.0.

Example 23: Object Recognition Task Model The cognition—enhancing properties of compounds of this invention were estimated using an animal model of cognition i.e., object recognition task.

Male Wistar rats (~230 — 280 grams) were used as experimental animals. Four animals were housed in each cage. Animals were kept on 20 % food deprivation before one day and given water ad libitam hout the experiment and maintained on a 12 hours light/dark cycle. The rats were habituated to individual arenas for 20 hour in the absence of any objects.

One group of 12 rats received vehicle (1 mL/kg) orally and r set of animals received compound of the formula (I) orally thirty s prior to ar (T1) and choice trial (T2).

The experiment was carried out in a 50 x 50 x 50 cm open field made up of acrylic.

During the familiarization phase (T1), the rats were placed individually in the open field for 3 s, in which two identical objects (plastic bottles, 12.5 cm height x 5.5 cm diameter) covered in yellow masking tape alone (a1 and a2) were positioned in two adjacent comers (10 cm from the walls). After 24 hours of the (T1) trial, the same rats were placed in the same arena as they were placed in T1 trial. During the choice phase (T2) rats were allowed to explore the open field for 3 minutes in presence of one familiar object (a3) and one novel object (b) (Amber color glass bottle, 12 cm high and 5 cm in diameter).

During the T1 and T2 trial, explorations of each object (defined as sniffing, licking, chewing or having moving sae whilst directing the nose towards the object at a distance of less than 1 cm) were recorded separately by stopwatch.

T1 is the total time spent exploring the familiar objects (a1 + a2).

T2 is the total time spent ing the familiar object and novel object (a3 +b). nce: Behavioural Brain Research, 1988, 31, 47—59.

Table 4: Object Recognition Task data Exploration time mean i S.E.M e Dose mg/kg, (sec) Inference No [7.0.

Familiar object Novel object Example 24: Non-Clinical Toxicology The safety of the example 1 of instant invention and comparator example of US7378415 were evaluated in repeated dose toxicity study in rat.

Female rats were used as experimental animals for evaluating the toxicity profile of example 1 of instant invention and the comparator e of 415.

During the study, female rats were dosed at incremental doses for minimum of 4 days. Toxicity assessment was done on the mortality, clinical observation, change in the body , feed consumption, al and anatomical pathology. Systemic exposures were also estimated for both of the compounds. All quantitative les are compared with control group using one—way ANOVA followed by Dunnet’s post—hoc test on GraphPad Prism Software version 4, 2003.

Table 5: Rat toxicity data M . Repeated dose ax1mum Compoun (4/7-Day) Tolerated Findings Tox1c1ty. . me AUC (NOAEL, mg/kg) N0 death up > 300 4'Day "peat "’X ' 38100 to the highest 2420 Example 1 NOAEL 300 ng*h/m mg/kg tested dose of ng/mL m /kg g 300 mg/kg 32:15:??? ity at P 4050 2100 mg/kg 7—Day repeat tox - 2 of 30 mg/kg ng*h/m US737841 "dim:0f NOAEL 30 mg/kg ngZ/mL Results: In tested preclinical species, example 1 showed surprisingly superior safety profile as compared to the comparator example of US7378415. In study where example 1 was dosed, no deaths were ed at doses as high as 300 mg/kg and the plasma exposures reaching as high as 38100 ng*h/mL (AUC). On the contrary, in the study where the comparator example of US7378415 evaluated, deaths were observed at doses >100 mg/kg on second day of dosing and the plasma concentrations were noted was as low as 4050 ng*h/mL (AUC).

Example 25: Evaluation of acetylcholine modulation in ventral hippocampus of male Wistar rats Experimental Procedure: Four groups of male Wistar rats (240—300 g body weight) were stereotaxically implanted with a microdialysis guide cannula in ventral hippocampus (AP: —5.2 mm, ML: + 5.0 mm, DV: —3.8 mm) under isoflurane anesthesia. Co—ordinates were taken according to atlas for the rat brain (Paxinos and Watson 2004) with nce points taken from bregma and al from the skull. The rats were allowed to recover individually for four— five days in a round bottom Plexiglas bowl with free access to feed and water.

After surgical recovery of 4—5 days, male Wistar rats were connected to dual quartz lined two—channel liquid swivel (Instech, UK) on a counter balance lever arm, which allowed unrestricted movements of the animal. Sixteen hours before start of study, a pre— equilibrated microdialysis probe (4 mm dialysis membrane) was ed into the ventral hippocampus through the guide cannula. On the day of study, probe was perfused with artificial cerebrospinal fluid (aCSF; NaCl 147 mM, KCl 3 mM, MgClz 1 mM, CaClz. 2H20 1.3 mM, NaHzPO4.2HZO 0.2 mM and NazHPO4.7HZO 1 mM, pH 7.2) at a flow rate of 1.5 uL/min and a ization period of 2 h was maintained. Five basal samples were collected at 20 min als prior to the treatment of example 1 (10 mg/kg, p.0.) or vehicle.

For two groups of the male Wistar rats, zil (1 mg/kg, s.c.) was administered 30 min after administration of example 1 and for another group of rats zil (1 mg/kg, s.c.) + memantine (1 mg/kg, s.c.) combination administered 30 min after administration of example 1. Dialysate samples were collected for an additional period of 4 h post treatment of example 1. Dialysates were stored below —50°C prior to analysis.

Quantitation of choline Acetylcholine in dialysate was quantified using LC—MS/MS method in the ation range of 0.099 nmol/L — 70.171 nmol/L. tical analysis All microdialysis data for acetylcholine was plotted as percent change from mean dialysate basal concentrations with 100 % defined as the average of five pre—dose values.

The percent change in acetylcholine levels were compared with donepezil alone and donepezil or memantine combination using two—way is of variance (time and ent), followed by Bonferroni’s posttest. Area under the curve (AUC) values for percent change in acetylcholine levels were calculated and the statistical icance between the mean AUC value were compared against donepezil alone or donepezil and memantine combination treatment using one—way ANOVA followed by Dunnett’s test.

Statistical icance was considered at a p value less than 0.05. Incorrect probe placement was ered as ia to reject the data from animal.

Reference: Paxinos G. and Watson C. (2004) Rat brain in stereotaxic coordinates.

Academic Press, New York.

Results: (1) Treatment with donepezil (1 mg/kg, s.c.) produced an increase in hippocampal choline levels and reached to the maximum of 888 i 85 % of basal levels. Example 1 (10 mg/kg, pa.) in combination with zil (1 mg/kg, s.c.) produced significant increase in acetylcholine levels and peak levels reached up to 1445 i 247 % of pre—dose levels (Figure la).

Mean area under the curve values (AUC) calculated after combination treatment of example 1 (10 mg/kg, pa.) and donepezil were significantly higher compared to donepezil (1 mg/kg, s.c.) alone (Figure lb). (11) Treatment with zil (1 mg/kg, s.c.) and ine (1 mg/kg, s.c.) combination produced an increase in hippocampal acetylcholine levels to the maximum of 1170 i 270 % of basal levels. Example 1 (10 mg/kg, pa.) in combination with donepezil (1 mg/kg, s.c.) and memantine (1 mg/kg, s.c.) produced significant increase in acetylcholine levels and peak levels reached up to 2822 i 415 % of pre—dose levels (Figure 2 (a)).

Mean area under the curve values (AUC) calculated after treatment of example 1 (10 mg/kg, p.0.), donepezil (1 mg/kg, s.c.) and memantine (1 mg/kg, s.c.) were significantly higher compared to donepezil (1 mg/kg, s.c.) and memantine (1 mg/kg, s.c.) combination (Figure 2 (b)).

We

Claims (1)

Claim:

1. A fluoropiperidine compound of a (1), 0 O 0%! / R3 / I R1