US20150111853A1

US20150111853A1 - Cephalosporin compositions and methods of manufacture

Info

Publication number: US20150111853A1
Application number: US14/521,421
Authority: US
Inventors: Jan-Ji Lai; Pradip M. Pathare; Laxma Kolla; Adrien F. Soret
Original assignee: Calixa Therapeutics Inc
Current assignee: Merck Sharp and Dohme LLC
Priority date: 2013-03-14
Filing date: 2014-10-22
Publication date: 2015-04-23
Also published as: US20140274999A1; US20140274958A1; WO2014152763A1; US9006421B2

Abstract

Provided herein is a method for the synthesis of cephalosporin antibiotic compounds comprising the conversion of a protected 7-amino group into a 7-carboxamide moiety in a single step.

Description

RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No. 61/782,365, filed Mar. 14, 2013. The entire content of this application is incorporated herein by reference in its entirety.

TECHNICAL FIELD

The present disclosure relates to cephalosporin compositions and the manufacture thereof.

BACKGROUND

Cephalosporin compounds containing the chemical substructure of formula (I) are important antibacterial therapeutic agents. The manufacture of these cephalosporin compounds is typically performed in a series of synthetic chemical reactions. Reducing the number of synthetic chemical reactions and associated purification steps can increase product yield and decrease the time for production, thereby increasing efficiency and decreasing production costs.
Syntheses of antibiotic cephalosporin compounds containing the substructure of formula (I) typically require two reactions for the formation of a 7-carboxamide moiety: (1) deprotection (i.e., removal of a protecting group) of the 7-amino group, and (2) acylation of the 7-amino group to form the 7-carboxamide moiety. One example of this two-step procedure is disclosed in U.S. Pat. No. 5,134,138 (see FIG. 2). Most cephalosporin antibiotics can be manufactured in an analogous way. Ceftolozane (CXA-101, FR264205) is a cephalosporin antibiotic compound, a synthesis of which is disclosed in U.S. Pat. No. 7,129,232. Additional cephalosporin antibiotic compounds include the compounds of Table 2. There remains an unmet need to identify novel manufacturing processes for synthesizing cephalosporin compounds comprising the chemical substructure of formula (I), including methods for formation of a 7-carboxamide moiety from a protected 7-amino group with fewer chemical synthetic steps.

SUMMARY

A novel chemical process useful in the manufacture of cephalosporin compounds containing the chemical substructure of Formula (I) can include deprotection (i.e., removal of a nitrogen protecting group) and acylation of the 7-amino group in a single step rather than multiple steps. The invention is based in part on the surprising discovery that salicyladehyde imine derivatives according to formula (Ia) can be reacted with activated carboxylic acid derivatives (Ib) to yield 7-carboxamide compounds according to formula (I) in a single step. This outcome is surprising because the imine derivatives of formula (Ia) are stable to the reaction conditions in the absence of the activated carboxylic acid derivative.
Accordingly, provided herein is a method for transforming a protected 7-amino group into a 7-carboxamide moiety comprising a single step.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts a representative 7-carboxamide moiety and 7-amino group.

FIG. 2 depicts a prior art procedure (U.S. Pat. No. 5,134,138) comprising the deprotection of a protected 7-amino group followed by conversion of the 7-amino group into a 7-carboxamide moiety.

FIG. 3 depicts the full scan mass spectrum of compound (IV-1).

FIG. 4 depicts the product ion mass spectrum of compound (IV-1).

FIG. 5 depicts the full scan mass spectrum of compound (III-1).

FIG. 6 depicts the product ion mass spectrum of compound (III-1).

FIG. 7 depicts the full scan mass spectrum of compound (II-1).

FIG. 8 depicts the product ion mass spectrum of compound (II-1).

FIG. 9 depicts the full scan mass spectrum of ceftolozane trifluoroacetate.

FIG. 10 depicts the product ion mass spectrum of ceftolozane trifluoroacetate.

FIG. 11 depicts the HPLC chromatograms of Example 2.

DETAILED DESCRIPTION

Provided herein is a method for preparing a compound of formula (II), or a salt thereof, comprising the step of reacting a compound of formula (III), or a salt thereof, with a compound of formula (IV), or a salt thereof, under suitable conditions to form a compound of formula (II), or a salt thereof, wherein the compounds of formulas (II), (III) and (IV) are defined according to the variable values below.

Variable R₁

In certain embodiments, R₁is R_1′—Z; wherein R_1′is selected from the group consisting of a bond, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, and heteroaryl; wherein Z is 0-2 instances of a substituent that for each occurrence is independently selected from the group consisting of hydrogen, halogen, hydroxyl, hydroxyalkyl, aminoalkyl, alkyl, alkylidenyl, alkenyl, heteroalkyl, cyano and amino, wherein Z is optionally, independently substituted one or more times with amino, halogen, carboxyl, carboxamide, oxo, a nitrogen protecting group, an oxygen protecting group or —P(O)(OZ′)₂; and wherein Z′ is independently hydrogen or an oxygen protecting group.
In one embodiment, R₁is selected from the group consisting of aryl and heteroaryl moieties. In certain embodiments, R₁is a substituted or unsubstituted aryl or heteroaryl moiety selected from the group consisting of: thiophene, furan, thiazole, tetrazole, thiadiazole, pyridyl, phenyl, phenol, cyclohexadiene and dithietane. In a particular embodiment, R₁is selected from the group consisting of the following moieties:
and salts thereof, wherein Z′ is defined above.
In a particular embodiment, R₁is
and the compound of formula (II) has the structure of formula (IIa).

Variable R₂

In certain embodiments, R₂is selected from the group consisting of hydrogen and alkoxy. In another embodiment of the method, R₂is hydrogen, and the compound of formula (II) has the structure of formula (IIb).

Variable Y

In certain embodiments, Y is selected from the group consisting of a bond, CH₂, CH₂S, SCH₂, C═C(H)CH₂CO₂R′, CH(OR′), C═N(OR′), CHNR″₂and C═NR″; wherein R′ is selected from the group consisting of hydrogen, an oxygen protecting group and alkyl, wherein the alkyl is optionally substituted one or more times with halogen, hydroxyl or —CO₂R₅; wherein R″ is a substituent that for each occurrence is selected from hydrogen, alkyl, C(O)heterocyclyl, and a nitrogen protecting group, wherein any two R″ substituents may combine to form a ring or a single nitrogen protecting group; and wherein R₅is independently hydrogen or an oxygen protecting group.
In one embodiment of the method, Y is selected from a bond, CH₂, CH₂S and C═C(H)CH₂CO₂R′, and R′ is selected from the group consisting of hydrogen and an oxygen protecting group. In another embodiment, Y is C═N(OR′) and R′ is selected from the group consisting of an oxygen protecting group, hydrogen, methyl, ethyl, CH₂CO₂R₅and C(CH₃)₂CO₂R₅. In yet another embodiment, Y is CH(OR′) and R′ is hydrogen or an oxygen protecting group. In still another embodiment, Y is CHNR″₂and R″ is 1-2 instances of a substituent that for each occurrence is selected from hydrogen, a nitrogen protecting group and
In a particular embodiment, Y is C═N(OR′) and R′ is C(CH₃)₂CO₂ ^tBu, and the compound of formula (II) has the structure of formula (IIc).

Variable R₃

In certain embodiments, R₃is selected from the group consisting of hydrogen and an oxygen protecting group. In another embodiment of the method, R₃is an oxygen protecting group selected from benzyl ethers. Benzyl ethers may be substituted (e.g., with one or more alkoxy substituents) or unsubstituted. In a particular embodiment, R₃is
(i.e., 4-methoxybenzyl, PMB, MPM).

Variables R₄and R_4′

R₄and R_4′are independently selected from the group consisting of halogen, —R₆-R₇, —CH₂—R₆-R₇and —CH═R₇; wherein R₆is selected from the group consisting of a bond, oxygen, sulfur, alkyl, alkenyl, aryl, heteroaryl and heterocyclyl; wherein R₇is selected from the group consisting of hydrogen, alkyl, alkenyl, alkanoyl, aroyl, heteroaroyl, carboxamide, aryl, heteroaryl and heterocyclyl; and wherein R₇is optionally, independently substituted 1-3 times with a substituent selected from alkyl, alkyl sulfite, heterocyclyl and NR_aR_b; wherein R_aand R_bare independently selected from the group consisting of hydrogen, alkyl, a nitrogen protecting group and C(O)NHR_c; wherein R_cis an alkyl group or a heteroalkyl group; and wherein R₄and R_4′are optionally, independently substituted one or more times with an oxygen protecting group or a nitrogen protecting group.
In another embodiment of the method, R₄and R_4′ are independently selected from the group consisting of hydrogen, chlorine, methyl, CH═CH—CH₃, CH═CH₂, CH₂OC(O)CH₃, CH₂OC(O)NH₂, CH₂OCH₃,
wherein A^⊖, for each occurrence, is independently a pharmaceutically acceptable anion. In certain embodiments, A^⊖is selected from chloride, acetate, trifluoroacetate and bisulfate. In a particular embodiment, A^⊖is trifluoroacetate.
In a particular embodiment, R₄is
In another particular embodiment, R_4′is

Variable X

In certain embodiments, X is selected from the group consisting of halogen, —OC(O)R₈and —OSO₂R₈; wherein R₈is selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl. In another embodiment of the method, X is —OSO₂R₈. In a particular embodiment, X is —OSO₂CH₃.

Methods of the Invention

In one aspect, provided herein is a method for preparing a compound of formula (II), or a salt thereof,
comprising the step of reacting a compound of formula (III), or a salt thereof,
with a compound of formula (IV), or a salt thereof,
in a mixture comprising an organic solvent and water, to form a compound of formula (II), or a salt thereof; wherein:
R₁is R_1′—Z, wherein R_1′is selected from the group consisting of a bond, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, and heteroaryl; and Z is 0-2 instances of a substituent that for each occurrence is independently selected from the group consisting of hydrogen, halogen, hydroxyl, hydroxyalkyl, aminoalkyl, alkyl, alkylidenyl, alkenyl, heteroalkyl, cyano and amino, wherein Z is optionally, independently substituted one or more times with amino, halogen, carboxyl, carboxamido, oxo, a nitrogen protecting group, an oxygen protecting group or —P(O)(OZ′)₂; and wherein Z′ is independently hydrogen or an oxygen protecting group;
Y is selected from the group consisting of a bond, CH₂, CH₂S, SCH₂, C═C(H)CH₂CO₂R′, CH(OR′), C═N(OR′), CHNR″₂and C═NR″; wherein R′ is selected from the group consisting of hydrogen, an oxygen protecting group and alkyl, wherein the alkyl is optionally substituted one or more times with halogen, hydroxyl or —CO₂R₅, and wherein R₅is independently hydrogen or an oxygen protecting group; and wherein R″ is a substituent that for each occurrence is selected from hydrogen, alkyl, C(O)heterocyclyl, and a nitrogen protecting group, wherein any two R″ substituents may combine to form a ring or a single nitrogen protecting group;
R₂is selected from the group consisting of hydrogen and alkoxy;
R₃is selected from the group consisting of hydrogen and an oxygen protecting group; and
R₄and R_4′are each independently selected from the group consisting of halogen, —R₆-R₇, —CH₂—R₆-R₇and —CH═R₇; wherein R₄and R_4′are optionally, independently substituted one or more times with an oxygen protecting group or a nitrogen protecting group;
R₆is selected from the group consisting of a bond, oxygen, sulfur, alkyl, alkenyl, aryl, heteroaryl and heterocyclyl;
R₇is selected from the group consisting of hydrogen, alkyl, alkenyl, alkanoyl, aroyl, heteroaroyl, carboxamide, aryl, heteroaryl and heterocyclyl; and wherein R₇is optionally, independently substituted 1-3 times with a substituent selected from alkyl, alkyl sulfite, heterocyclyl and NR_aR_b; wherein
R_aand R_bare independently selected from the group consisting of hydrogen, alkyl and C(O)NHR_c;
R_cis alkyl or heteroalkyl; and wherein
X is selected from the group consisting of halogen, —OC(O)R₈and —OSO₂R₈, wherein R₈is selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl.
In one embodiment of the method, R₁is selected from the group consisting of:
In another embodiment of the method, R₂is hydrogen.
In another embodiment of the method, Y is selected from a bond, CH₂, CH₂S and C═C(H)CH₂CO₂R′ and R′ is selected from the group consisting of hydrogen and an oxygen protecting group, or wherein Y is C═N(OR′) and R′ is selected from the group consisting of an oxygen protecting group, hydrogen, methyl, ethyl, CH₂CO₂R₅and C(CH₃)₂CO₂R₅and R₅is hydrogen or an oxygen protecting group, or wherein Y is CH(OR′) and R′ is hydrogen or an oxygen protecting group, or wherein Y is CHNR″₂and R″ is 1-2 instances of a substituent that for each occurrence is selected from hydrogen, a nitrogen protecting group and
In another embodiment of the method, R₃is an oxygen protecting group that is a benzyl ether. In a particular embodiment, R₃is paramethoxybenzyl (PMB).
In another embodiment of the method, R₄and R_4′are selected from the group consisting of hydrogen, chlorine, methyl, CH═CH—CH₃, CH═CH₂, CH₂OC(O)CH₃, CH₂OC(O)NH₂, CH₂OCH₃,
wherein each occurrence of A^⊖is independently an anion.
In another aspect, provided herein is a method for preparing a compound of formula (II), or a salt thereof,
comprising the step of reacting a compound of formula (III), or a salt thereof,
with a compound of formula (IV), or a salt thereof,
in a mixture comprising an organic solvent and water, to form a compound of formula (II), or a salt thereof; wherein:
R₁is selected from the group consisting of:
wherein Z′ is independently hydrogen or an oxygen protecting group;
Y is selected from the group consisting of:

—CH₂—,

wherein R′ is selected from the group consisting of hydrogen and an oxygen protecting group;
R₂is hydrogen;
R₃is selected from the group consisting of hydrogen and an oxygen protecting group; and
R₄and R_4′are each independently selected from the group consisting of:

and —CH═CH₂,

wherein each occurrence of A^⊖is independently an anion, and
X is —OSO₂R₈, wherein R₈is selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl.
In one embodiment of the above methods, further comprises the step of reacting the compound of formula (II), or a salt thereof, with a strong acid to form a compound of formula (V), or a salt thereof, wherein the compound of formula (V) is selected from the compounds of Table 2. The strong acid can be a Bronsted acid (e.g., trifluoroacetic acid, hydrochloric acid), or a Lewis acid (e.g., TiCl₄). In a particular embodiment, the strong acid is trifluoroacetic acid.
Also provided herein are particular embodiments of the method (a)-(h), wherein:
(a) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(b) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(c) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(d) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(e) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(f) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

(g) wherein the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

and
(h) the compound of formula (III) has the structure:

- the compound of formula (II) has the structure:

and

- the compound of formula (V) has the structure:

Compositions

In another aspect, provided herein is a composition comprising the compound of formula (V), or salt a thereof, and one or more compound selected from the group consisting of: the compound of formula (II), or salt a thereof, the compound of formula (III), or salt a thereof, and the compound of formula (IV), or salt a thereof. In one embodiment, the composition comprises the compound of formula (V), or salt a thereof, the compound of formula (I) or salt a thereof, the compound of formula (Ia) or salt a thereof, and the compound of formula (Ib) or salt a thereof. In another embodiment of the composition, the compound of formula (II), or salt a thereof, the compound of formula (III), or salt a thereof, and the compound of formula (IV), or salt a thereof, are present, if at all, in an amount that is less than or equal to 0.05% w/w. In yet another embodiment of the composition, the compound of formula (II), or salt a thereof, the compound of formula (III), or salt a thereof, and the compound of formula (IV), or salt a thereof, are present, if at all, in an amount that is less than or equal to 0.05 mol %. In another aspect, provided herein is a method of treating a bacterial infection in a patient, comprising the step of administering a composition as described above.
In still another aspect, provided herein is a composition comprising a compound of formula (V), or a salt thereof, selected from the compounds of Table 2, or salts thereof, prepared according to a method described herein. Provided herein are particular embodiments of the composition (i)-(p), wherein:
(i) the compound of formula (V-1), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof;
(j) the compound of formula (V-2), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof;
(k) the compound of formula (V-3), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof;
(I) the compound of formula (V-5), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

, or a salt thereof; and
or a salt thereof;
(m) the compound of formula (V-6), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof;
(n) the compound of formula (V-9), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof;
(o) the compound of formula (V-26), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof; and
(p) the compound of formula (V-16), or a salt thereof:
and

- 0.3-0.5% of one or more compound selected from:

or a salt thereof; and
or a salt thereof.

Uses and Methods of Treatment

In another aspect, provided herein is a method of treating a bacterial infection in a patient, comprising the step of administering to the patient a composition of embodiments (i)-(p). In another aspect, provided herein is a composition of embodiments (i)-(p) for use in the treatment of a bacterial infection in a patient. In another aspect, provided herein is the use of a composition of embodiments (i)-(p) for the manufacture of a medicament for the treatment of a bacterial infection in a patient.
In another aspect, provided herein is a composition comprising two or more compounds selected from the group consisting of:
(a) the compound of formula (II-1), or a salt thereof
(b) the compound of formula (III-1), or a salt thereof
(c) the compound of formula (IIIc), or a salt thereof
(d) the compound of formula (IV-1), or a salt thereof
and
(e) the compound of formula (IVb), or a salt thereof
In one embodiment, the composition further comprises the compound having the structure:
or a salt thereof.

Compounds of the Invention

Provided herein is a compound having the structure:
wherein A^⊖ is an anion.
Also provided herein is a compound having the structure:
wherein X is selected from the group consisting of halogen, —OC(O)R₈and —OSO₂R₈, wherein R₈is selected from the group consisting of alkyl, heteroalkyl, aryl and heteroaryl.
Particular embodiments of the compounds of formulas (II), (III) and (IV) are listed in Table 1. For example, in the synthesis of the antibiotic compound ceftolozane, the compounds of formulas (II), (III) and (IV) can have the structures of formulas (II-1), (III-1) and (IV-1), respectively.
In one embodiment, the compound of formula (IV-1) is prepared from the compound of formula (IVa):
by a process comprising the steps of: (a) forming a mixture comprising potassium carbonate and the compound of formula (IVa); and (b) adding methansulfonyl chloride to the mixture of step (a) such that the compound of formula (IV-1) is formed.

Synthesis

In one embodiment of the method, the suitable conditions comprise reacting in a mixture comprising an organic solvent and water. Organic solvents can be selected from the group consisting of aromatic solvents, aliphatic solvents, halogenated solvents, halogenated aromatic solvents, halogenated aliphatic solvents, ethers, halogenated ethers, esters and amides. In a particular embodiment, the organic solvent is selected from halogenated solvents. In another particular embodiment, the organic solvent is dichloromethane.
In another embodiment of the method, the suitable conditions comprise reacting in a mixture comprising an organic solvent and about 6-9 percent (w/w) water relative to the compound of formula (III), or salt thereof. In a particular embodiment, the suitable conditions comprise reaction in a mixture comprising an organic solvent and about 6-8 percent (w/w) water relative to the compound of formula (III), or salt thereof. In still another embodiment, the suitable conditions comprise reacting in a mixture comprising dichloromethane and about 6-9 percent of water relative to the compound of formula (III), or salt thereof.
Notably, the compound of formula (III) is hydrolytically stable under the reaction conditions, in the absence of the compound of formula (IV). As shown in FIG. 11 and described in Example 2, compound (III-1) was combined with dichloromethane and water in the same relative amounts as in Example 1. Upon stirring for four hours, no hydrolysis of (III-1) was observed. In contrast, under the same solvent, temperature and time conditions, but in the presence of compound (IV-1), compound (III-1) reacts to form compound (II-1).
In some embodiments, the method further comprises the step of reacting the compound of formula (II), or a salt thereof, under suitable conditions to form a compound of formula (V), or a salt thereof, wherein the compound of formula (V) is selected from the compounds of Table 2, or salts thereof. In some embodiments, the suitable conditions comprise reacting the compound of formula (II) with strong acid. In a particular embodiment, the strong acid is trifluoroacetic acid.

DEFINITIONS

Pharmaceutically acceptable salts are known to those of skill in the art. In some of the embodiments described herein, the compounds of formulas (II) and (III) are trifluoroacetate salts.
Oxygen and nitrogen protecting groups are known to those of skill in the art. Oxygen protecting groups include, but are not limited to methyl ethers, substituted methyl ethers (e.g., MOM (methoxymethyl ether), MTM (methylthiomethyl ether), BOM (benzyloxymethyl ether), PMBM or MPM (p-methoxybenzyloxymethyl ether), to name a few), substituted ethyl ethers, substituted benzyl ethers, silyl ethers (e.g., TMS (trimethylsilyl ether), TES (triethylsilylether), TIPS (triisopropylsilyl ether), TBDMS (t-butyldimethylsilyl ether), tribenzyl silyl ether, TBDPS (t-butyldiphenyl silyl ether), to name a few), esters (e.g., formate, acetate, benzoate (Bz), trifluoroacetate, dichloroacetate, to name a few), carbonates, cyclic acetals and ketals. Nitrogen protecting groups include, but are not limited to, carbamates (including methyl, ethyl and substituted ethyl carbamates (e.g., Troc), to name a few) amides, cyclic imide derivatives, N-alkyl and N-aryl amines, benzyl amines, substituted benzyl amines, trityl amines, imine derivatives, and enamine derivatives, for example.
Exemplary anions include, but are not limited to, carboxylates (e.g., acetate, benzoate, trifluoroacetate), halides (e.g., chloride, bromide, iodide), sulfate (e.g., monosulfate, bisulfate) and phosphate (e.g., monophosphate).
In some embodiments, alkyl groups and groups comprising an alkyl group (e.g., alkoxy, alkanoyl, alkylamino, aminoalkyl, heteroalkyl) comprise 1-6 carbon atoms. In some embodiments, aryl groups and groups comprising aryl groups (e.g., aroyl) comprise 6-12 carbon atoms. In some embodiments, heteroaryl groups and groups comprising heteroaryl groups (e.g., heteroaroyl) comprise 1-10 carbon atoms and 1-4 heteroatoms selected from oxygen, nitrogen and sulfur.

TABLE 1

	Formula (II)	Formula (III)	Formula (IV)

1


2


3


4


5


6


7


8


9


10


11


12


13


14


15


16


17


18


19


20


21


22


23


24


25


26


27


28


29


30


31


32

TABLE 2

	Formula (V)

V-1

V-2

V-3

V-4

V-5

V-6

V-7

V-8

V-9

V-10

V-11

V-12

V-13

V-14

V-15

V-16

V-17

V-18

V-19

V-20

V-21

V-22

V-23

V-24

V-25

V-26

V-27

V-28

V-29

V-30

V-31

V-32

EXAMPLES

Materials and Instrumentation

Compound characterization was obtained by high resolution mass spectrometry (HRMS) and high resolution mass spectrometry/mass spectrometry (HR MS/MS). Samples were dissolved in solution and the sample solutions were directly infused into time-of-flight (TOF) mass spectrometer to obtain parent (MS) and product scans (MS/MS) of analyte. Suitable materials and instrumentation are known to persons of skill in the art.

Example 1

Synthesis of Compound (V-1)

(1) Synthesis of compound (IV-1): (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)acetic methanesulfonic anhydride

A 5.0 liter reactor was charged with N,N-dimethylacetamide (1.4 L). Solid (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)acetic acid (250 g, 1 eq., prepared according to the method disclosed in U.S. Pat. No. 7,129,232) was added to the reactor at ambient temperature and the mixture was stirred until the solid was dissolved. The solution was cooled to about 4° C. (target: 2-5° C.) and stirred for another 10-15 minutes. Potassium carbonate (106.7 g, 184.9 mmol, 1.1 eq.) was added to the reactor in one portion. Methanesulfonyl chloride (118.0 mL, 2.2 eq.) was added to the reactor at a rate of about 5 mL/min while maintaining the batch temperature <10° C. The reaction was stirred for 1-2 hours at about 6° C., then cooled to about 0-5° C. Ethyl acetate (2.5 L, 10 volumes) was added to the reactor while maintaining a temperature of about 0-5° C. 1.6% HCl (aq) (1.35 L) was added to the reactor, maintaining a temperature of about 10-15° C. The biphasic mixture was agitated and the layers were then separated. The organic layer was washed with sodium chloride solution, dried with sodium sulfate and concentrated under reduced pressure to obtain crude material. The crude material was dissolved in ethyl acetate (150 mL) and filtered over silica gel. The filtrate was concentrated under reduced pressure to yield the title compound (299 g, 96.7%) as a colorless solid. Exact Mass: 408.08. HRMS: 409.0846 (M+1).

(2) Synthesis of compound (III-1): 5-amino-4-(3-(2-((tert-butoxycarbonyl)amino)ethyl)ureido)-2-(((6R,7R)-7-((Z)-(2-hydroxybenzylidene)amino)-2-(((4-methoxybenzyl)oxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-1-methyl-1H-pyrazol-2-ium trifluoroacetate

Compound (III-1) was prepared by coupling the compound (6R,7R)-4-methoxybenzyl 3-(chloromethyl)-7-((Z)-(2-hydroxybenzylidene)amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (purchased from Nippon Chemicals, Japan) with the compound tert-butyl (2-(3-(1-methyl-5-(tritylamino)-1H-pyrazol-4-yl)ureido)ethyl)carbamate (UBT, prepared according to the method disclosed in U.S. Pat. No. 7,129,232).
In a reactor, UBT (274 g) was dissolved in 1 L of N-methylpyrrolidone (NMP) at 35-45° C. The solution was cooled to 15-20° C. SCLE (200 g) was added to the solution and stirred until it was completely dissolved. Then added 104 mL of N,O-Bis(trimethylsilyl)acetamide (BSA) dropwise in 30 minutes, followed by addition of 98.2 g potassium iodide (KI) in 6-8 portions, and maintained the temperature between 20-25° C. The resulting mixture was stirred at 15-25° C. for about 45-50 hours. The forgoing solution was then slowly added to 5% sodium triflouro acetate (4 L) at room temperature in 3 hours and precipitates were formed. The slurry was filtered and washed with 2 L deionized water for 4 times, and 4 L of heptanes for 3 times. The wet cake was dried under nitrogen with vacuum until it reached a constant weight. The resulting compound (III-1) was isolated as a light yellow solid (569 g, 86.5%). Exact Mass (-TFA):977.40. HRMS:977.4025 (M+).

(3) Synthesis of compound (II-1): 5-amino-2-(((6R,7R)-7-((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)acetamido)-2-(((4-methoxybenzyl)oxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-4-(3-(2-((tert-butoxycarbonyl)amino)ethyl)ureido)-1-methyl-1H-pyrazol-2-ium trifluoroacetate

A reactor was charged with compound (III-1) (150 g), water (11.25 mL), compound (IV-1) (60 g), and dichloromethane (265 mL). The mixture was stirred for three hours at room temperature, then added to methyl tertiary butyl ether (1.5 L) over the course of 2-3 hours, resulting in the formation of a solid. The solid was filtered and the filter cake was washed with additional methyl tertiary butyl ether (1.0 L). The solid was dried under vacuum to yield the title compound (142.1 g, 81.2%). Exact Mass: 943.36 (-TFA). HRMS: 943.3555 (M+).

(4) Synthesis of Ceftolozane Trifluoroacetate

Compound (II-1) was dissolved in dichloromethane. Trifluoroacetic acid and anisole were added and the reaction was stirred for about 3 hours. Methyl tertiary butyl ether was added, causing the formation of a precipitate. The precipitate was collected by filtration and dried under vacuum to yield the title compound. Exact Mass (−TFA): 667.18. HRMS: 667.1810 (M+).

(5) Synthesis of Compound (V-1)

Ceftolozane trifluoroacetate (5 g) was dissolved in water (40 mL) and filtered. The solution was purified by HPLC using a Waters Sunfire C18 (50×100 mm, 5 μm) column with an eluent comprising Solvent A: acetonitrile+0.08% sulfuric acid (v/v) and Solvent B: water+0.08% sulfuric acid (v/v).

Example 2

Compound (III-1) (2.12 g) was dissolved in dichloromethane (3.75 ml). Water (160 μL) was added and the mixture was stirred for four hours, with hourly monitoring by HPLC

Example 3

Synthesis of (6R,7R)-7-((Z)-2-(ethoxyimino)-2-(5-(phosphonoamino)-1,2,4-thiadiazol-3-yl)acetamido)-3-((4-(1-methylpyridin-1-ium-4-yl)thiazol-2-yl)thio)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

A reactor is charged with 4-(2-(((7R)-7-((Z)-(2-hydroxybenzylidene)amino)-2-(((4-methoxybenzyl)oxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)thio)thiazol-4-yl)-1-methylpyridin-1-ium trifluoroacetate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(5-(phosphonoamino)-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 4

Synthesis of (6R,7R)-7((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(hydroxyimino)acetamido)-8-oxo-3-((E)-((R)-2-oxo-[1,3′-bipyrrolidin]-3-ylidene)methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

A reactor is charged with (7R)-4-methoxybenzyl-3-((E)-((R)-1′-(tert-butoxycarbonyl)-2-oxo-[1,3′-bipyrrolidin]-3-ylidene)methyl)-7-((Z)-(2-hydroxybenzylidene)amino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((4-methoxybenzyl)oxy)imino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 5

Synthesis of (6R,7R)-7-((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

A reactor is charged with 1-(((7R)-7-((Z)-(2-hydroxybenzylidene)amino)-2-(((4-methoxybenzyl)oxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)pyridin-1-ium trifluoroacetate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 6

Synthesis of (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

A reactor is charged with 1-(((6R,7R)-7-((Z)-(2-hydroxybenzylidene)amino)-2-(((4-methoxybenzyl)oxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-1-methylpyrrolidin-1-ium trifluoroacetate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 7

Synthesis of (6R,7R)-7-(2-(1H-tetrazol-1-yl)acetamido)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

A reactor is charged with (6R,7R)-4-methoxybenzyl 7-((Z)-(2-hydroxybenzylidene)amino)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (1 eq), water (6-9 weight % relative to the Schiff base), 2-(1H-tetrazol-1-yl)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 8

Synthesis of (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-((carboxymethoxy)imino)acetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

A reactor is charged with (6R,7R)-4-methoxybenzyl 7-((Z)-(2-hydroxybenzylidene)amino)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(2-aminothiazol-4-yl)-2-((2-(tert-butoxy)-2-oxoethoxy)imino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Example 9

Synthesis of (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(((2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

A reactor is charged with (6R,7R)-4-methoxybenzyl 7-((Z)-(2-hydroxybenzylidene)amino)-3-(((2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (1 eq), water (6-9 weight % relative to the Schiff base), (Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetic methanesulfonic anhydride (2.5 eq) and dichloromethane (1.75 mL per gram of Schiff base). The mixture is stirred for three hours at room temperature, then added to methyl tertiary butyl ether over the course of 2-3 hours, resulting in the formation of a solid. The solid is filtered and the filter cake was washed with additional methyl tertiary butyl ether. The filtered solid is deprotected using conventional methods and dried under vacuum to yield the title compound.

Claims

1-13. (canceled)

14. A composition comprising a compound of formula (V), or a salt thereof, selected from the compounds of Table 2, or salts thereof, prepared according to the method of claim 5.

15. The composition of claim 14, comprising:

(a) the compound of formula (V-1), or a salt thereof: