Synthesis of intermediate (XI) of Scheme 25142902e: Racemic 2,4-diaminobutyric acid (I) was esterified in MeOH in the presence of SOCl2. The resulting methyl ester (II) was cyclized using Dowex 2x8-400 resin to give 3-amino-2-pyrrolidinone (III), which was converted to the trifluoroacetamide (IV) using methyl trifluoroacetate in MeOH. The lactam nitrogen of (IV) was then protected with benzyl chloroformate and lithium hexamethyldisilazide yielding (V). Reduction of (V) with NaBH4, followed by treatment with ethanolic H2SO4 provided ethoxypyrrolidine (VI). Ethyl isovalerate (VII) was converted to the silyl enolate (VIII) employing lithium hexamethyldisilazide and silyl triflate. Coupling of (VIII) with ethoxypyrrolidine (VI) in the presence of BF3-Et2O provided (IX). After hydrolysis of the trifluoroacetamide group of (IX) with K2CO3 yielding (X), its cyclization by means of tert-butylmagnesium chloride yielded the pyrrolopyrrolone system. Separation of the required (3aS, 6aR)-isomer (XI) was achieved by chiral HPLC.
Alternative synthesis of intermediate (XI) of Scheme 25142902e: In an alternative procedure, (R)-asparagine (XII) was protected as the trifluoroacetamide (XIII) and then esterified by means of AcCl in MeOH yielding (XIV). Dehydration of the amide function of (XIV) employing tosyl chloride and pyridine produced nitrile (XV). The catalytic hydrogenation of (XV) with concomitant cyclization of the intermediate amine generated the chiral pyrrolidinone (XVI), which was protected with benzyl chloroformate and n-BuLi to give (XVII). This was converted to the intermediate (XI) by means of a sequence analogous to that for the racemic pyrrolidinone (IV).
Alternative synthesis of intermediate (XVII) of Scheme 25142902b: In a further procedure, (R)-methionine (XXI), was protected as the Boc derivative (XXII). Subsequent treatment of (XXII) with Boc2O and then with ammonium bicarbonate yielded amide (XXIII), which was condensed with benzyl chloroformate to produce imide (XXIV). The S-alkylation with CH3I yielded sulfonium salt (XXV), which was then cyclized to pyrrolidinone (XXVI) in the presence of Dowex 2x8-400 resin. Acid deprotection of the Boc group of (XXVI), followed by condensation with methyl trifluoroacetate furnished intermediate (XVII) already described in Scheme 25142902b.
Synthesis of intermediate (XXX) of Scheme 25142902e: Alkylation of piperidine (XXVII) with ethyl 4-bromocrotonate (XXVIII) afforded tertiary amine (XXIX). Acid hydrolysis of the ethyl ester of (XXIX) then provided carboxylic acid (XXX).
The intermediate pyrrolopyrrolone (XI) was converted to the methanesulfonamide (XXXI) upon treatment with mesyl chloride and lithium hexamethyldisilazide. Removal of the benzyloxycarbonyl group of (XXXI) by hydrogenolysis over Pd(OH)2 produced amine (XXXII). This was coupled with piperidinylbutenoic acid (XXX) using EDC and HOBt to yield the target compound, which was finally converted to the hydrochloride salt.
Synthesis of silyl enol ether intermediate (XIII): The reaction of ethyl isovalerate (XII) with triisopropylsilyl trifluoromethanesulfonate and 1,3-dimethylperhydropyrimidin-2-one by means of LiHMDS in THF gives the target silyl enol ether (XIII).
The reaction of D-methionine (XIV) with Boc2O in dioxane gives the N-protected methionine (XV), which is treated with Boc2O, pyridine and ammonium bicarbonate to yield the methioninamide (XVI). The reaction of (XVI) with benzyl chloroformate (XVII) by means of BuLi in DMF/pyridine affords the carbamate (XVIII), which is treated with methyl iodide in acetone to provide the sulfonium salt (XIX). The cyclization of (XIX) by means of Dowex 2XB-400 (OH form) in acetonitrile gives the N-protected pyrrolidinone (XX), which is deprotected with HCl in dioxane to yield the amino compound (XXI). Finally, this compound is acylated with methyl trifluoroacetate (XXII) and NMM in dichloromethane to afford the target pyrrolidinone intermediate (XXIII).
The reaction of D-asparagine (XXIV) with methyl trifluoroacetate (XXII) in methanol gives N-(trifluoroacetyl)-D-asparagine (XXV), which is esterified with MeOH and Ac-Cl, yielding the methyl ester (XXVI). The reaction of (XXVI) with TsCl and pyridine in dichloromethane affords the 3-cyanopropionic ester (XXVII), which is cyclized by hydrogenation over a Rh/Al2O3 catalyst in ethanol to provide the pyrrolidinone (XXVIII). Finally, this compound is condensed with benzyl chloroformate and BuLi in THF to furnish the target pyrrolidinone intermediate (XXIII). Assembly of the target compound: The reductive methylation of intermediate pyrrolidinone (XXIII) by means of LiBH4 in THF, followed by treatment with EtOH and conc. H2SO4, gives 2-ethoxy-3(R)-(trifluoroacetamido)pyrrolidine-1-carboxylic acid benzyl ester (XXIX), which is condensed with the intermediate silyl enol ether (XIII) by means of BF3/Et2O in dichloromethane to yield the adduct (XXX). The deprotection of the amino group of (XXX) with K2CO3 in ethanol/water yields the aminopyrrolidine (XXXI), which is cyclized by means of t-butylmagnesium bromide and TMEDA in THF to afford the bicyclic compound (XXXII). The reaction of the free NH group of (XXXII) with methanesulfonyl chloride and LiHMDS in THF provides the cyclic methanesulfonamide (XXXIII), which is decarboxylated by hydrogenation with H2 over Pd/C in dioxane/ethyl acetate to give the bipyrrolidine derivative (XXXIV). Finally, this compound is condensed with the oxazole intermediate (IX) by means of HOBT and DEC in acetonitrile.
The reaction of D-methionine (I) with tert-butoxycarbonyl anhydride and NaOH in water gives the N-protected compound (II), which is treated with more tert-butoxycarbonyl anhydride and ammonium bicarbonate in pyridine/DMF yielding The N-protected methioninamide (III). The protection of the amide group of (III) with benzyloxycarbonyl chloride and BuLi in THF affords the fully protected methioninamidde (IV), which by reaction with methyl iodide in acetone or acetonitrile gives the dimethylsulfonium iodide (V). The cyclization of (V) by means of DOWEX 2X8-400 (hydroxide form) yields the protected 3-aminopyrrolidinone (VI), which by selective deprotection with HCl followed by acylation with methyl trifluoroacetate and NaHCO3 affords N-[1-(benzyloxycarbonyl)-2-oxopyrrolidin-3(R)-yl]trifluoroacetamide (VII). The reduction of the carbonyl group of (VII) with LiBH4 in THF provides the pyrrolidinol (VIII), which is treated with ethanol and conc. H2SO4 giving the ethyl ether (IX). The condensation of (IX) with the triisopropylsilyl derivative of ethyl 3-methylbutyrate (X) by means of BF3 ethearate in dichloromethane yields the 2-pyrrolidinylbutyrate (XI) as predominant isomer, which is destrifluoroacetylated with K2CO3 in refluxing ethanol/water affording aminopyrrolidine (XII). The cyclization of (XII) by means of tert-butylmagnesium chloride in THF gives a mixture of bicyclic pyrrolidones, from which the chiral isomer (XIII) was separated by crystallization. The mesylation of (XIII) with methanesulfonyl chloride and lithium hexamethyldisylazane in THF affords the sulfonamide (XIV), which is deprotected by hydrogenation with H2 over Pd(OH)2 in ethyl acetate/dioxane giving the bicyclic pyrrolidone (XV), which is finally acylated with 4-(1-piperidinyl)-2(E)-butenoic acid (XVI) by means of HOBT and triethylamine in acetonitrile or oxlayl chloride in dichloromethane.