Patent Application
20060178391
The present invention is directed to a method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives.
Indole-2,3-dione-3-oxime derivatives are useful pharmaceutical products. WO 98/14447 (NeuroSearch) describes indole-2,3-dione-3-oxime derivatives useful for antagonising the effect of excitatory amino acids. These compounds are prepared by conventional methods of chemical synthesis including the step of reacting an 1H-indol-2,3-dion with an amino derivative. More specifically WO 98/14447 describes indole-2,3-dione-3-oxime derivatives, some of which exist as racemic mixtures.
It is often desirable, and sometimes subject to regulatory demands, to undertake drug development on specific enantiomers rather than racemic drugs. This rationale is based on the findings that often the desired characteristics of chiral compounds reside with one of its enantiomers, while the other enantiomer might in fact add to a potential toxicological effect of the drug.
In order to allow thorough investigation of each enantiomer, processes for obtaining enantiopure preparations of chiral compounds are of significant importance for drug development.
EP 439779 (Chisso Corp.) describes a process for producing optically active hydroxy lactones using enzymatic transesterification. However, a method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives is not described.
EP 467132 (Chisso Corp.) describes 4-substituted-2-hydroxybutanoates and a process for producing them. However, a method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives is not described.
The present invention is directed to a novel method for obtaining enantiopure preparations of chiral indole-2,3-dione-3-oxime derivatives.
Thus, in its first aspect, the invention provides a method of obtaining enantiopure preparations of chiral indole-2,3-dione-3-oxime derivatives (Compounds A or B), which method comprises the subsequent steps of
(i) Reacting an 8-amino-1,2,3,4-tetrahydro-isoquinoline (Compound 9) derivative with chloral hydrate and hydroxylamine hydrochloride to give an N-(1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-hydroxyimino-acetamide (Compound 10) derivative (Step 9);
(ii) Adding sulphuric acid to the N-(1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-hydroxyimino-acetamide (Compound 10) derivative obtained in step (i) (Step 10); and
(iii) Reacting the 2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinoline (Compound 11) derivative obtained in step (ii) with chiral (enantiopure (R) or (S)) α-N,N-diBoc-aminoxy-γ-butyrolactone to obtain the desired chiral end product, i.e. enantiopure (R)— or (S)-2-[2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]4-hydroxy-butyric acid) (Compound A or B) (Step 11);
followed by recovery of the desired end product.
In another aspect the invention provides a method of preparing the enantiopure starting material for use according to the method of the invention which method comprises the subsequent steps of
(i) acetylating a racemic mixture of α-hydroxy-γ-butyrolactone to obtain racemic α-acetoxy-γ-butyrolactone (Step 1);
(ii) subjecting the racemic α-acetoxy-γ-butyrolactone obtained in step (i) to enzymatic de-acetylation to obtain enantiopure (S) or (R) α-acetoxy-γ-butyrolactone (Step 2); and
(iii) subjecting the enantiopure (S) or (R) α-acetoxyy-γ-butyrolactone obtained in step (ii) to hydrolysis using acidic ion-exchange (Step 3);
followed by recovery of the desired end product.
Other objects of the invention will be apparent to the person skilled in the art from the following detailed description and examples.
The present invention provides a method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives. The indole-2,3-dione-3-oxime derivatives obtained according to the method of the invention may in particular be characterised by the general Formula IA or IB
wherein
R represents hydrogen, alkyl or benzyl; and
R4 represent hydrogen or alkyl; and
R5 represents phenyl, which phenyl may optionally be substituted one or more times with substituents selected from the group consisting of halogen, CF3, NO2, CN, NH2, alkyl, alkoxy and SO2NR51R52; wherein
R51 and R52, independently of each another represent hydrogen or alkyl; or
R51 and R52 together with the N-atom to which they are attached form a piperidinyl- or morpholinyl-ring; and
R6 and R7 together form a benzo-fused ring of the formula
—NR8—CH2—CH2—CH2—;
—CH2—NR8—CH2—CH2—;
—CH2—CH2—NR8—CH2—; or
—CH2—CH2—CH2—NR8—;
wherein R8 represents hydrogen or alkyl.
In a more preferred embodiment the indole-2,3-dione-3-oxime derivative obtained according to the method of the invention is characterised by Formula IIA or IIB
wherein
R represents hydrogen or alkyl;
R5 represents phenyl, which phenyl is optionally substituted with halogen, CF3, NO2, CN or SO2NR51R52; wherein
R51 and R52, independently of each another represent hydrogen or alkyl; or
R51 and R52 together with the N-atom to which they are attached form a piperidinyl- or morpholinyl-ring; and
R8 represents hydrogen or alkyl.
In an even more preferred embodiment the indole-2,3-dione-3-oxime derivative obtained according to the method of the invention is characterised by Formula IIIA or IIIB
wherein
R represents hydrogen or alkyl;
R53 represents SO2NR51R52; wherein
R51 and R52, independently of each another represent hydrogen or alkyl; or
R51 and R52 together with the N-atom to which they are attached form a piperidinyl- or morpholinyl-ring; and
R8 represents hydrogen or alkyl.
In an even more preferred embodiment the indole-2,3-dione-3-oxime derivative obtained according to the method of the invention is characterised by the general Formula IIIA or IIIB, wherein
R represents hydrogen or C1-3-alkyl;
R53 represents SO2NR51R52; wherein
R51 and R52, independently of each another represent hydrogen or C1-3-alkyl; or
R51 and R52 together with the N-atom to which they are attached form a piperidinyl- or morpholinyl-ring; and
R8 represents hydrogen or C1-6-alkyl.
In a most preferred embodiment the indole-2,3-dione-3-oxime derivative obtained according to the method of the invention is Compound IVA or IVB
The present invention provides a method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives, in particular the indole-2,3-dione-3-oxime derivatives described above.
In a preferred embodiment the method of the invention comprises the subsequent steps of
(i) Reacting an 8-amino-1,2,3,4-tetrahydro-isoquinoline (Compound 9) derivative with chloral hydrate and hydroxylamine hydrochloride to give an N-(1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-hydroxyimino-acetamide (Compound 10) derivative (Step 9);
(ii) Adding sulphuric acid to the N-(1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-hydroxyimino-acetamide (Compound 10) derivative obtained in step (i) (Step 10); and
(iii) Reacting the 2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinoline (Compound 11) derivative obtained in step (ii) with chiral (enantiopure (R) or (S)) α-N,N-diBoc-aminoxy-γ-butyrolactone to obtain the desired chiral end product, i.e. enantiopure (R)— or (S)-2-[2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]-4-hydroxy-butyric acid) (Compound A or B) (Step 11);
followed by recovery of the desired end product.
In a preferred embodiment the method further comprises the step of
(a) reacting enantiopure (S) or (R) α-hydroxy-γ-butyrolactone with N,N-diBoc-hydroxylamine to give enantiopure (S) or (R) α-N,N-diBoc-aminoxy-γ-butyrolactone (Step 8a);
followed by steps (i) to (iii) as described above.
In another preferred embodiment the method further comprises the step of
(b) subjecting N,N-diBoc-O-benzylhydroxylamine to hydrogenation to give N,N-diBoc-hydroxylamine (Step 7);
followed by step (a) and steps (i) to (iii) as described above.
In a third preferred embodiment the method further comprises the step of
(c) converting O-benzylhydroxylamine into N,N-diBoc-O-benzylhydroxylamine using Boc2O (Step 6);
followed by step (b), step (a), and steps (i) to (iii) as described above.
In a fourth preferred embodiment the method further comprises the step of
(d) reacting enantiopure (S) or (R) α-hydroxy-γ-butyrolactone with tosyl chloride to give enantiopure (S) or (R) α-tosyloxy-γ-butyrolactone (Step 5);
followed by step (c), step (b), step (a), and steps (i) to (iii) as described above.
In a most preferred embodiment the 8-amino-1,2,3,4-tetrahydro-isoquinoline (Compound 9) derivative of step (i) is 4-(8-amino-2-methyl-1,2,3,4-tetrahydro-isoquinolin-5-yl)-N,N-dimethyl-benzenesulfonamide (to obtain N-[5-(4-dimethylsulfamoyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolin-8-yl]-2-hydroxyimino-acetamide); and
the 2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinoline (Compound 11) derivative of step (iii) is N,N-dimethyl-4-(8-methyl-2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinolin-5-yl)-benzenesulfonamide;
giving enantiopure (R)- or (S)-2-[5-(4-dimethylsulfamoyl-phenyl)-8-methyl-2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]-4-hydroxy-butyric acid as the end product (Compound A or B).
Preparation of the Starting Materials
In another aspect the invention provides a method of producing the enantiopure starting materials for use according to the method described above.
The method of the invention for preparing the starting materials is characterised by comprising the subsequent steps of
(i) acetylating a racemic mixture of α-hydroxy-γ-butyrolactone to obtain racemic α-acetoxy-γ-butyrolactone (Step 1);
(ii) subjecting the racemic α-acetoxy-γ-butyrolactone obtained in step (i) to enzymatic de-acetylation to obtain enantiopure (S) or (R) α-acetoxy-γ-butyrolactone (Step 2); and
(iii) subjecting the enantiopure (S) or (R) α-acetoxy-γ-butyrolactone obtained in step (ii) to hydrolysis using acidic ion-exchange (Step 3);
followed by recovery of the desired end product, i.e. the enantiopure (S) or (R) α-hydroxy-γ-butyrolactone.
In a preferred embodiment the method further comprises the step of
(iv) subjecting the enantio-impure remainings of step (iii), i.e. the enantio-impure α-hydroxy-γ-butyrolactone and α-acetoxy-γ-butyrolactone, to racemisation using acid or base;
followed by re-entry of the racemic mixture into step (i).
In a more preferred embodiment the enzymatic de-acetylation of step (ii) is carried out using a lipolytic enzyme. In a most preferred embodiment the lipolytic enzyme is Lipase PS (available from Amano Pharmaceutical Co.).
The invention is further illustrated with reference to the following example, which is not intended to be in any way limiting to the scope of the invention as claimed.
First the synthetic route to the optical isomers of 2-[5-(4dimethylsulfamoyl-phenyl)-8-methyl-2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]-4-hydroxy-butyric acid, hereinafter designated Compounds IVA and IVB, is outlined.
Synthesis of the Chiral Building Blocks
Synthesis of the N,N-DiBoc Protected Hydroxylamine Part
Synthesis of the isatin Derivative
Synthesis of Enantiopure (R)-E-1 and (S)-E-1
Next, a more detailed description of each step of the synthesis is presented.
Step 1
A mixture of racemic α-hydroxy-γ-butyrolactone (25 g; 0.25 mol), DMAP (1.5 g), acetylchloride (25.5 ml; 0.37 mol) in CH2Cl2 (325 mL) was added solid K2CO3 (50 g) in portions (slightly exothermic). The reaction mixture was stirred at room temperature overnight, filtered and evaporated to dryness. Column chromatography (Petrol ether 80-100:EtOAc=2:1) gave 26.4 g (75%) racemic α-acetoxy-γ-butyrolactone.
Step 2
A mixture of racemic a-acetoxyy-butyrolactone (29.8 g; 0.207 mol) and Amano's Lipase PS (800 mg) in THF/water (200 mL; 10/1) was stirred at room temperature overnight. The reaction mixture was filtered and evaporated to dryness. The crude product was dissolved in CH2Cl2 (250 mL) and extracted with cold water (5×50 mL). The organic phase was dried (MgSO4), filtered and evaporated to dryness to yield 12.6 g (43%) enantiopure (S)-α-acetoxy-γ-butyrolactone.
The combined aqueous phases were washed with CH2Cl2 (5×50 mL). The aqueous phase was evaporated to dryness, added CH2Cl2, dried (MgSO4), filtered and evaporated to dryness to give 8.5 g (40%) (R)-α-hydroxy-γ-butyrolactone. Overall yield by moles; 83%. [α]D25=+65.7°.
Step 3
A suspension of enantiopure (S)-α-acetoxy-γ-butyrolactone (5 g, 34.7 mmol) and Amberlite IRA120 (acid form) in H2O (50 mL) was heated to reflux and reaction progress monitored by GCMS. After 2 hours, GCMS indicated complete transformation. The reaction mixture was filtered and evaporated to dryness. Vacuum distillation 0.3-0.4 mbar (b.p. 85-92° C.) afforded the enantiopure (S)-α-hydroxy-γ-butyrolactone (2.6 g, 76% yield). [α]D25=−66.1°.
The crude product may also be isolated from the aqueous solution by extraction with CH2Cl2 and the pure product alternatively be isolated by column chromatography. Amberlite IRA-120 may be substituted by H2SO4, however with an overall lower yield.
Step 4
Enantio-impure remainings of α-hydroxy-γ-butyrolactone and α-acetoxy-γ-butyrolactone from step 3 may be recycled by racemisation using acid or base, followed by re-entry into steps 1 to 3.
Step 5
A suspension of (R)-α-hydroxy-γ-butyrolactone (3.5 g, 34.3 mmol), tosyl chloride (10.0 g, 52.6 mmol), and K2CO3 (2.23 g, 16.2 mmol) in dry CH2Cl2 (50 mL) was stirred at room temperature overnight. The reaction mixture was filtered, and the filtrate washed with 1M phosphate buffer pH=7 (2×50 mL), 3 M NaCl (aq.) (1×50 mL), dried with Na2SO4, filtered and evaporated to dryness to give the crude product. The crude product was triturated by PE40/60 (50 mL) and stirred for 30 minutes. The precipitate formed was isolated by filtration and washed with PE40/60 to remove trace amounts of tosyl chloride, to give 7.7 g (87%) of enantiopure (R)-α-tosyloxy-γ-butyrolactone. [α]36525=−9.9°.
The (S)-isomer was prepared similarly. [α]36525+9.8°.
Step 6
A suspension of O-benzylhydroxylamine hydrochloride (30 g, 188 mmol) in acetonitrile (150 mL) was added triethylamine (29 mL). The thick suspension was stirred for 60 minutes at room temperature and filtered. The precipitate was washed with acetonitrile (100 mL) on the filter. The combined filtrates were added to a cooled (0° C.) solution of Boc2O (45 g, 207 mmol) in acetonitrile (150 ml), over 20 minutes. The reaction mixture was stirred at 0° C., and allowed slowly to warm up to room temperature. The reaction mixture was left with stirring at room temperature overnight, when 1H-NMR indicated complete conversion of O-benzylhydroxylamine into N-Boc-O-benzylhydroxylamine.
The reaction mixture was added a solution of Boc2O (6.7 g, 310 mmol) in acetonitrile (150 mL), followed by a solution of DMAP (2 g, 16.4 mmol) in acetonitrile (30 mL). The reaction mixture was then stirred at 40° C. until TLC (EtOAc:PE60/80=1:5) indicated complete conversion of the intermediate N-Boc-O-benzylhydroxylamine (approx. 2 hours). The reaction mixture was evaporated to dryness and re-dissolved in EtOAc (200 mL). The organic phase was washed with a mixture of 1M phosphate buffer pH=7 (100 mL) and NaCl (aq., sat.) (50 mL). The organic phase was dried with Na2SO4, filtered and evaporated to dryness to give an oil, which precipitated upon trituration by PE40/60 (20 mL). The precipitated was isolated by filtration to give 56 g (92%) of N,N-diBoc-O-benzylhydroxylamine as a white solid.
Step 7
A suspension of N,N-diBoc-O-benzylhydroxylamine (15 g, 46.4 mmol) and 5% Pd/C (0.9 g) in 96% EtOH was subjected to hydrogenation at atmospheric pressure. When 390 mL H2 was consumed, hydrogenation was stopped. The reaction mixture was filtered through celite and evaporated to dryness to give 12.5 g of an orange oil composed of N,N-diBoc-hydroxylamine and N,N-diBoc-imide (86:14).
The oil was dissolved in EtOAc (25 mL) and extracted with 1M NaOH (3×25 mL). The combined aqueous phases were immediately poured into a 1M phosphate buffer pH=7 and extracted with EtOAc (3×75 mL). The combined organic fractions were dried with Na2SO4, filtered and evaporated to dryness. The isolated white solid was air dried to give 8.8 g (81%) of pure N,N-diBoc-hydroxylamine.
Step 8a
A solution of N,N-diBoc-hydroxylamine (8.5 g, 36 mmol) in dry THF (50 mL) under N2 was added Ph3P (11 g, 42 mmol) and cooled to 0° C. A solution of (S)-α-hydroxy-γ-butyrolactone (3.6 g, 35 mmol) in dry THF (10 mL) was added, followed by addition of DEAD (6.8 ml, 42 mmol) during 30 minutes. The dark reaction mixture was stirred at 0° C. until TLC (EtOAc:PE60/80=1:2, KMnO4 spray) indicated complete conversion of (S)-α-hydroxy-γ-butyrolactone (approx. 2 hours).
The reaction mixture was evaporated to dryness, dissolved in Et2O (50 mL) and triturated by addition of PE40/60 (100 mL). The reaction mixture was filtered, and the precipitate thoroughly washed with Et2O:PE40/60=1:1 (100 mL). The combined organic filtrates were evaporated to dryness to give 16 g of brown oil. The oil was subjected to column chromatography. (1000 mL SiO2, 7 cm in diameter, eluent: EtOAc:PE60/80=1:2). The pure fractions were combined, evaporated to dryness and washed with PE40/60 (15 mL) to give 8.5 g (77%) of enantiopure (R)-α-N,N-diBoc-aminoxy-γ-butyrolactone.
(R)-isomer: [αD25=+62.5°; [α]36525=+210°.
The (R)-isomer was prepared similarly: [αD25=−62.8°; [α]36525=−211°.
Step 8b
A suspension of 60% NaH (350 mg, 8.8 mmol) in dry CH2Cl2 under N2 at 0° C. was added a solution of BocNHOH in CH2Cl2 (5 mL). The reaction mixture was stirred at 0° C. for 30 minutes, where after a solution of (R)-α-tosyloxy-γ-butyrolactone (2 g, 7.8 mmol) in CH2Cl2 (5 mL) was added. The reaction mixture was allowed to warm up to room temperature, and left with stirring overnight. The reaction mixture was quenched with 1M phosphate buffer pH=6.3 (20 mL) and the organic phase separated. The aqueous phase was extracted with CH2Cl2 (2×20 mL), and the combined organic fractions extracted with NaCl (aq., sat.) (15 mL). The organic fraction was dried with Na2SO4, filtered and evaporated to dryness. Column chromatography (150 g SiO2, eluent: EtOAc:PE60/80=1:2) gave 1.5 g (89%) of (S)-α-N-Boc-aminoxy-γ-butyrolactone. [αD25=−42°; [α]36525=−127°.
In a similar way the (R)-isomer, containing approximately 10% of (S)-isomer, was prepared: [α]36525=+70°.
Steps 9-10
Purification
Chloral hydrate (71.6 g, 0.434 mol), hydroxylamine hydrochloride (60.3 g, 0.868 mol) and Na2SO4 (243.3 g, 1.65 mol) were added in sequence to a reaction vessel containing H2O (1.8 L) preheated to 80° C. When a clear solution was achieved, the aniline (4-(8-amino-2-methyl-1,2,3,4-tetrahydro-isoquinolin-5-yl)-N,N-dimethyl-benzenesulfonamide; 99.0 g, 0.217 mol) was added. The reaction was stirred for 45 minutes when TLC showed full consumption of the aniline. Celite (39 g) was added and the reaction mixture was cooled to 40° C. and stirred for 1 hour. The reaction mixture was filtered and the precipitate washed with cold H2O (500 mL). The isolated solid material (isonitrosoacetanilide on celite) was dried under a heating lamp to give 132 g material, which was used without further purification.
The crude isonitrosoacetanilide derivative (N-[5-(4-dimethylsulfamoyl-phenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolin-8-yl]-2-hydroxyimino-acetamide) obtained above was added over 45 minutes to a solution of H2SO4 (350 mL), preheated to 75° C. During the addition, the reaction temperature increased to 80-85° C. After complete addition, the reaction was stirred for another 30 minutes at a reaction temperature of 75-85° C., when all the isonitrosoacetanilide was consumed (TLC, CH2Cl2:acetone:MeOH=4:1:1).
The reaction mixture (i.e. N,N-dimethyl-4-(8-methyl-2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinolin-5-yl)-benzenesulfonamide and 4-(3-hydroxyimino-8-methyl-2-oxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinolin-5-yl)-N,N-dimethyl-benzenesulfonamide) was poured onto H2O (3.5 L), heated to reflux and then filtered warm to remove celite. The celite was washed with boiling water (750 mL), and the combined aqueous fractions allowed cooling slowly overnight for precipitation. The precipitate was filtered off, washed with H2O (2×250 mL) and 96% EtOH (2×250 mL) and then air dried to give 69.8 g (67%) of crude isatin derivative as the hydrosulfate. The crude product contained 11.4% (typically 9-13%) of the oxime.
Crude product (38.1 g, 76.7 mmol) was suspended in H2O (800 mL) and pH adjusted to 13 using 4 M NaOH (approx. 80 mL) to give a purple solution, which was stirred for 20 minutes. The then yellow-orange solution was added THF (300 mL) and pH adjusted to 8.5 using AcOH. This solution was washed with EtOAc (4×400 mL), then added conc. H2SO4 (90 mL) and heated to 75° C. The aqueous solution was allowed to slowly cool to room temperature and then 0° C. The precipitate formed was filtered off, then washed with H2O (2×100 mL) and 96% EtOH (2×100 mL) to give 31.3 g (corresponding to approx. 53% yield from the aniline) of the pure isatin derivative as the hydrosulfate.
Step 11
A suspension of the isatin derivative (i.e. N,N-dimethyl-4-(8-methyl-2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinolin-5-yl)-benzenesulfonamide) as the hydrosulfate (32.5 g, 65.4 mmol) was suspended in H2O (650 mL). The reaction mixture was heated to 60° C. and pH adjusted to 1.5 using 2M H2SO4 (aq.). A solution of (R)- or (S)-α-N,N-diBoc-aminoxy-γ-butyrolactone (23 g, 72.5 mmol) in THF (130 mL) was added. The thick reaction mixture was stirred at 60° C. for 9 hours, when HPLC indicated complete consumption of the isatin derivative.
The reaction mixture was left overnight at room temperature, warmed to 40° C. and pH adjusted to 10 using 1M NaOH (aq.) (approx. 150 mL). Further 1M NaOH (aq.) (approx. 180 mL overall) was added during the reaction to keep pH at 10. After stirring for 4 hours at 40° C., the reaction mixture became a nearly clear solution. HPLC indicated that all product, in intermediate lactone form was consumed, and pH was adjusted to 8.5 using 2M H2SO4 (aq.).
The reaction mixture was evaporated to dryness to yield 40.3 g solid. The isolated solid was refluxed in a mixture of i-PrOH/H2O (85/15) (1600 mL) and filtered warm (inorganic salts are removed). The filtrate was allowed to slowly cool to 0° C., and left overnight. The precipitate formed, was isolated by filtration to give 23.9 g yellow to orange crystals. The crystals (20 g) was dissolved in H2O (80 mL) and stirred vigorously with EtOAc (250 mL) for 1½ hour (to remove the Z-isomer and remainings of the isatin oxime). The organic phase was discarded, and the aqueous phase was evaporated to dryness. The solid material isolated was suspended in THF (400 mL) and filtered.
The precipitate was dissolved in H2O (160 mL) and pH adjusted slowly to 5.2 using 2M H2SO4 (aq.). The mixture was stirred 1½ hour at room temperature and filtered. The isolated solid was washed with cold H2O (2×25 mL) and air dried to give A or B (i.e. (R)— or (S)-2-[5-(4-dimethylsulfamoyl-phenyl)-8-methyl-2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]-4-hydroxy-butyric acid) as a yellow amorphous solid, 15.8 g (56%). The reaction occurs with retention of stereochemistry, i.e. no inversion is observed.
Step 12
A suspension of isatin derivative 12-1 (i.e. N,N-dimethyl-4-(8-methyl-2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinolin-5-yl)-benzenesulfonamide) as the hydrosulfate (3.5 g, 7 mmol) in 96% EtOH (100 ml) was added hydroxylammonium chloride (1 g, 14 mmol) and then refluxed for 2½ hours. As the starting material was not completely consumed (TLC), further hydroxylammonium chloride (0.3 g, 2.1 mmol) was added. The reaction mixture was left at reflux over night.
The reaction mixture was cooled and filtered, and the precipitate washed with 96% EtOH. The precipitate was suspended in H2O (100 ml), warmed to 75-80° C. and pH adjusted to 8.5 using 4 M NaOH (aq.). The aqueous solution was cooled to rt. and filtered. The precipitate was washed with H2O, then suspended in abs. EtOH (100 ml) and brought to reflux. The solution was cooled to room temperature and filtered.
The precipitate was washed with abs. EtOH and air dried to give 2.63 g (91%) of 12-2 (i.e. 8-methyl-5-(4-(N,N-dimethylsulphamoyl)-phenyl)-6,7,8,9-tetrahydro-1H-pyrrolo-[3,2-h]-isoquinoline-2,3-dione-3-oxime) as the free base. The free base darkens upon standing but may be stored as the hydrosulfate.
Step 13
A suspension of 60% NaH (50 mg, 1.25 mmol) in dry DMF (2 ml) under N2 at 0° C. was slowly added a solution of the isatin oxime, 8-methyl-5-(4-(N,N-dimethylsulphamoyl)-phenyl)-6,7,8,9-tetrahydro-1H-pyrrolo-[3,2-h]-isoquinoline-2,3-dione-3-oxime (500 mg, 1.25 mmol) in dry DMF (8 ml). The reaction mixture was stirred for 30 minutes at 0° C., where after a solution of (R)-α-tosyloxy-γ-butyrolactone (340 mg, 1.33 mmol) in dry DMF (2 ml) was added. The reaction was left with stirring at room temperature overnight, when HPLC indicated complete consumption of the isatin oxime.
The reaction mixture was evaporated to dryness and then added H2O (20 ml) and dioxane (5 ml). The reaction mixture was adjusted to pH=10 by use of 1M NaOH. Further NaOH was added to keep the pH at 10. The reaction mixture was left with stirring over night at room temperature and heated to 40-45° C. for 1 hour, when HPLC indicated complete conversion of the intermediate lactone. The reaction mixture was adjusted to pH=8.5 and evaporated to dryness (extensive foaming).
The isolated solid was refluxed in i-PrOH (15 ml) for 5 minutes, cooled to room temperature and filtered to give 610 mg of solid material. Part of the solid material (550 mg) was refluxed in a mixture of i-PrOH (15 ml) and H2O (0.75 ml) and cooled to 0° C. The precipitate formed was isolated by filtration to give 310 mg of crude material.
The mother liquor was mainly composed of sodium tosylate. The crude material (300 mg) was dissolved in H2O (10 ml) and pH adjusted to 5.7 using 1M HCl, alternatively 5.2 using 2M H2SO4 (aq.). An oil separates and H2O was removed be decantation. The product precipitates upon trituration by EtOH. The product was isolated by filtration, giving 160 mg (28%) of IVA or IVB (i.e. (R)— or (S)-2-[5-(4-dimethylsulfamoyl-phenyl)-8-methyl-2-oxo-1,2,6,7,8,9-hexahydro-pyrrolo[3,2-h]isoquinolin-3-ylideneaminooxy]-4-hydroxy-butyric acid).
The reaction occurs with inversion of stereochemistry, i.e. the stereocenter in α-tosyloxy-γ-butyrolactone is inverted.
| Number | Date | Country | Kind |
|---|---|---|---|
| PA200201237 | Aug 2002 | DK | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/DK03/00539 | 8/13/2003 | WO | 8/10/2005 |
