IE912683A1 - Dynemicin analogs: syntheses, methods of preparation and use - Google Patents

Dynemicin analogs: syntheses, methods of preparation and use

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Publication number
IE912683A1
IE912683A1 IE268391A IE268391A IE912683A1 IE 912683 A1 IE912683 A1 IE 912683A1 IE 268391 A IE268391 A IE 268391A IE 268391 A IE268391 A IE 268391A IE 912683 A1 IE912683 A1 IE 912683A1
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group
compound
fused
hydroxyl
ring
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IE268391A
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IE66159B1 (en
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Adrian L Smith
Chan-Kou Hwang
Sebastian V Wendeborn
Kyriacos C Nicolaou
Erwin P Schreiner
Wilhelm Stahl
Wei-Min Dai
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Scripps Research Inst
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Saccharide Compounds (AREA)

Abstract

2088499 9202522 PCTABS00010 A fused ring system compound is disclosed that contains an epoxide group on one side of the fused rings and an enediyne macrocyclic ring on the other side of the fused rings. The compounds have DNA-cleaving, antimicrobial and tumor growth-inhibiting properties. Chimeric compounds having the fused ring system compound as an aglycone bonded to (i) a sugar moiety as the oligosaccharide portion or (ii) a monoclonal antibody or antibody combining site portion thereof that immunoreacts with target tumor cells are also disclosed. Compositions containing a compound or a chimer are disclosed, as are methods of preparing a compound.

Description

THE SCRIPPS RESEARCH INSTITUTE, a Corporation organised under the laws of the State of California, United States of America, of 10666 North Torrey Pines Road, La Jolla, California 92037, United States of America.
The present invention relates to novel DNAcleaving, cytotoxic and anti-tumor compounds, and particularly to fused ring systems that contain an enediyne macrocyclic ring and also an epoxide ring, as well as chimeras that contain such a fused ring system Dynemicin A (Compound 1 shown below), where Me is methyl, is a potent antibacterial and anticancer agent recently isolated from Micromonospora cherslna [(a) Konishi et al, J. Am. Chem. Soc.. 112:3715-3716 (1990); (b) Konishi et al., J, Antibiot, 42:1449-1452 (1989)]. Its striking molecular structure combines characteristics of both the enediyne [Golik et al., J. Am. Chem. Soc.. 109:3461-3462 (1987); Golik et al., J. Am. Chem. Soc.. 109:3462-3464 (1987); Lee et al., J, Am. Chem. Soc.. 109:3464-3466 (1987); Ellestad et al., J. Am. Chem. Soc.. 109:3466-3468 (1987)] and the anthracycline [Anthracycline Antibiotics, H.S. El Khadem, ed., Academic Press, New York (1982) and Recent Aspects in Anthracyclinone Chemistry, Tetrahedron Symposia-in-Print No. 17, T.R. Kelly, ed., Tetrahedron; ££):4537-4794 (1984)] classes of antibiotics, and presents a considerable challenge to organic synthesis as well as a unique opportunity for the development of new synthetic technology and therapeutic agents.
The calicheamicin and esperamicin derivatives are perhaps the best known of the enediyne compounds.
For a key paper describing the first synthesis of calicheamicinone, see: (a) Cabal et al., J, Am. Chem. Soc.. 112:3253 (1990). For other selected studies of model systems in the area of calicheamicinsesperamicins, see: (b) Nicolaou et al, J. Am. Chem.
Soc.. 110:4866-4868 (1988); (c) Nicolaou et al., J. Am. Chem. Soc.. 110:7247-7248 (1988); (d) Schoenen et al., Tetrahedron Lett.. 30:3765-3768 (1989); (e) Magnus et al., J. Am. Chem. Soc.. 110:6921-6923 (1988; (f) Kende et al., Tetrahedron Lett.. 21:4217-4220 (1988).
Brief Summary of the Invention The present invention relates to novel fused ring systems that contain an epoxide ring and an enediyne macrocyclic ring, and thus have structural features similar to dynemicin A. The compounds have DNA-cleaving, antibiotic and antitumor activities.
Compositions and methods of making and using the compounds are disclosed.
A fused ring compound of the invention has a structure that corresponds to the formula wherein A is a double or single bond; R1 is selected from the group consisting of H, ¢,-¾ alkyl, phenoxycarbonyl, benzyloxycarbonyl, ¢,-¾ alkoxycarbonyl, substituted ¢,-¾ alkoxycarbonyl (particularly substituted ethoxycarbonyl), and 9-fluorenylmethyloxycarbonyl; R2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyloxy ¢,-¾ alkyl; R3 is selected from the group consisting of H and C,-C6 alkoxy; R4 is selected from the group consisting of H, hydroxyl, ¢,-¾ alkoxy, oxyacetic acid, oxyacetic ¢,-¾ hydrocarbyl or benzyl ester, oxyacetic amide, oxyimidazilthiocarbonyl and ¢,-¾ acyloxy; R6 and R7 are each H or together with the unsaturated carbon atoms of the intervening vinylene group form a one, two or three fused aromatic sixmembered ring system; W together with the carbon atoms of the depicted, intervening vinylene group forms a substituted aromatic hydrocarbyl ring system containing 1, 2 or 3 six-membered rings such that said fused ring compound contains 3, 4 or 5 fused rings, all but two of which are aromatic, and in which that aromatic hydrocarbyl ring system, W, is joined [a, b] to the structure shown (i.e., W is joined [a,b] to the nitrogen-containing rings of the structure shown); and R8 is hydrogen or methyl, with the proviso that R8 is hydrogen when W, together with the carbon atoms of the intervening vinylene group is 9,10-dioxoanthra.
In preferred practice, W together with the intervening vinylidene group forms a benzo ring so that a compound has the structural formula shown below. wherein R5 is selected from the group consisting of hydrogen, C,-C6 alkoxy, hydroxyl, acyloxy, oxyethanol, oxyacetic acid, s-nitrobenzyloxy and halo, and A and the remaining R groups are as before described.
More particularly, in one embodiment, R2, R3, R5, R7 and R8 are hydrogen so that a compound of the - 5 invention corresponds to the structural formula shown below, where R1 and R4 are as previously defined.
More preferably, R5 is alkoxy, hydroxyl, C.,-C6 acyloxy, oxyethanol, or oxyacetic acid, and R4 is hydrogen (H) or hydroxyl so that a fused ring compound has the structural formula shown below.
Also contemplated is a chimeric compound (also referred to as a chimer or chimera) that is comprised of a before-described fused ring compound as an aglycone portion bonded to (i) an oligosaccharide portion or (ii) a monoclonal antibody or antibody combining site portion thereof that immunoreacts with target tumor cells. - 6 The oligosaccharide portion comprises a sugar moiety selected from the group consisting of ribosyl, deoxyribosyl, fucosyl, glucosyl, galactosyl, N-acetylglucosaminyl, N-acetylgalactasaminyl, a saccharide whose structure is shown below, wherein a wavy line adjacent a bond indicates the position of linkage OMe A monoclonal antibody or binding site portion thereof is bonded to the fused ring compound aglycone portion through an R4 oxyacetic acid amide or ester bond, or an oxyacetic acid amide or ester bond from W.
An oligosaccharide portion is glycosidically bonded to the aglycone portion through the hydroxyl of an R4 oxyethanol group or the hydroxyl of an oxyethanolsubstituent of W.
A pharmaceutical composition is also 10 contemplated. That pharmaceutical composition contains a DNA cleaving, antibiotic or tumor cell growthinhibiting amount of a before-defined compound or chimera as active agent dissolved or dispersed in a physiologically tolerable diluent.
A compound, chimera or a pharmaceutical composition of either is also useful in a method for cleaving DNA, for inhibiting tumor growth and as an antimicrobial. In accordance with such a method, the DNA to be cleaved, target tumor cells whose growth is to be inhibited or target microbial cells is (are) contacted with a composition of the invention. That contact is maintained for a time period sufficient for the desired result to occur. Multiple administrations of a pharmaceutical composition can be made to provide the desired contact.
Brief Description of the Drawings In the drawings forming a portion of this disclosure, Figure 1 is a photograph of an ethidium bromide stained 1 percent agarose gel that illustrates the cleavage of 0X174 form I DNA by Compound 40 after 24 hours in phosphate buffers (50mM) containing 20 volume percent THF at pH 7.4. Lane 1 is the DNA alone as control, lanes 2-6 show the results obtained with 5000, - 9 2000, 1000, 500 and ΙΟΟμΜ Compound 40, respectively.
The designations I, II and III outside the gel indicate forms I, II and III of the DNA, respectively.
Figure 2 is a photograph of an ethidium 5 bromide stained 1 percent agarose gel that illustrates the cleavage of φΧ174 from I DNA by Compounds 40, 47, 42, 54, 55, 58 and 62 after 24 hours in pH 8.0 50mM Tris-HCl buffer. Lane 1 is the DNA alone as control, lanes 2, 3, 4, 5, 6, 7 and 8 show the results obtained with 5mM of each of compounds 40, 47, 42, 54, 55, 58 and 62, respectively. The designations Form I, II and III are as in Figure 1.
Figure 3 is a graph showing results from two studies of the percent growth inhibition of MIA PaCa-2 human pancreatic carcinoma cells over a four-day time period by various concentrations of Compound 2 (DY-1).
Figure 4 is a graph showing the results from four studies of the percent growth inhibition over a four-day time period of MB49 murine bladder carcinoma cells by various concentrations of Compound 2 (DY-1).
IC50 values for two of the studies were 43 nM and 91 nM.
Figure 5 is a graph showing the results from two studies of the percent growth inhibition over a four-day time period of MB49 murine bladder carcinoma cells by various concentrations of Compound 21 (DY-2).
Detailed Description of the Invention I. The Compounds A compound of the invention contains an 30 enediyne macrocycle linked to a fused ring that corresponds to structural Formula I wherein A is a double or single bond? R1 is selected from the group consisting of H, 0,-C^ alkyl, phenoxycarbonyl, benzyloxycarbonyl, alkoxycarbonyl, substituted alkoxycarbonyl (particularly a substituted ethoxycarbonyl) and 9-fluorenylmethyloxycarbonyl? R2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyloxy-C^-C^ alkyl; R3 is selected from the group consisting of H and alkoxy? R4 is selected from the group consisting of H, hydroxyl, C,-C6 alkoxy, oxyacetic acid (-OCH2CO2H) , hydrocarbyl or benzyl oxyacetic acid ester, oxyacetic amide, oxyethanol (-OCH2CH2OH), oxyimidazylthiocarbonyl and C,-^ acyloxy; R6 and R7 are each H or together with the intervening vinylene group form a one, two or three fused aromatic six-membered ring system; W together with the bonded, intervening, vinylene group (i.e., the unsaturated carbon atoms bonded to W) forms a substituted aromatic hydrocarbyl ring system containing 1, 2 or 3 six-membered rings such that said fused ring compound contains 3, 4 or 5 fused 6-membered rings all but two of which rings are - 11 aromatic, and in which that aromatic hydrocarbyl ring system, W, is joined [a, b] to the structure shown? and R8 is hydrogen or methyl with the proviso that R8 is hydrogen when W together with the intervening vinylidene group is 9,10-dioxoanthra.
Exemplary R6 and R7 groups are shown in Scheme III and are discussed in relation thereto, and thereafter.
As noted above, the bond, A, between the R2 and R3 substituents can be a double or single bond. The bond A is preferably a single bond.
A Cj-C^ alkyl group, as can be present in R1 is exemplified by methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, pentyl, 2-methylpentyl, hexyl, cyclohexyl, cyclopentyl and the like. A substituted alkyl group is also contemplated as an R1 group. Such substituted alkyl groups include hydroxyalkyl groups such as 2-hydroxyethyl, 4-hydroxyhexyl and 3-hydroxypropyl, haloalkyl groups such as 2-chlorobutyl, 3-halopentyl such as 3-fluoropentyl, and the like. The above alkyl and substituted C,-C6 alkyl groups are further contemplated as the alkyl portion of a carbonyloxy c,—C6 alkyl group of R2; i.e., a alkyl ester of a R2 carboxyl group, and of a R1 urethane group. Those same alkyl groups can constitute the alkyl portion of a C,-C6 alkoxy group of R3 or R4. A 0,-C^ acyloxy group as is present in R4 or R5 (discussed hereinafter) is a carboxylic acid derivative of an appropriate alkyl group, above, except for, for example, cyclohexyl and iso-propyl, and is limited to a cyclopentylcarboxyl group for the cyclopentane derivatives. Examples of such acyloxy groups include formyloxy, acetoxy, propionoxy, butyryloxy, isobutyryloxy, pentanoyloxy, 2-methylbutyryloxy, pivaloyloxy, hexanoyloxy, and the like. - 12 The alcohol-carbonyl portion of a urethane R1 is typically formed by the reaction of a corresponding halo formate derivative, such as a chloroformate like phenylchloroformate, with the secondary amine nitrogen atom that is formed by addition of an acetylenic groupcontaining moiety to the 6-position or a correspondingly numbered position of a fused ring system such as that shown in Scheme II hereinafter. Such groups can also be prepared by base-catalyzed exchange from a formed carbamate using the substituted ethyl alcohol as is illustrated hereinafter.
Exemplary C,-C6 alkoxycarbonyl groups and substituted C,-C6 alkoxycarbonyl groups contain a before-described C,-C6 alkoxy group or substituted C,-C6 alkoxy group linked to the carbonyl group and can be formed by reaction of a C,-C6 alkylchloroformate. Exemplary substituted ethoxycarbonyl groups that are a particularly preferred group of substituted C,-C6 alkoxycarbonyl group have a substituent other than hydrogen at the 2-position of the ethoxy group, and include 2-trimethylsilylethoxycarbonyl, 2-phenylsulfonylethoxycarbonyl, a- or β2-naphthylsulfonylethoxycarbonyl, a- or β2-anthracylsulfonylethoxycarbonyl, 2-propenoxycarbonyl, 2-hydroxyethoxycarbonyl, 2-triphenylphosphoniumethoxycarbonyl halide (e.g., chloride, bromide or iodide) and 2-trimethylammoniumethoxycarbonyl halide (as before).
It is particularly preferred that R1 be a group that can be enzymatically or otherwise removed intracellularly to provide the resulting secondary amine free of a substituent group. A compound where R1 contains a 2-substituted-ethoxycarbonyl group such as a 2-phenylsulfonyl-, 2-naphthylsulfonyl- and 2-anthracylsulfonyl- as are shown in Scheme III (shown - 13 as R, therein) can form the free secondary amine compound via a β-elimination under relatively mild conditions. Phenylsulfonylethoxycarbonyl, a-naphthyland /J-naphthylsulfonylethoxycarbonyl (collectively referred to as naphthylsulfonylethoxycarbonyl) are particularly preferred R1 groups, with phenoxycarboxyl being a preferred R1 group.
An R8 group can be methyl or hydrogen with the proviso that R8 is hydrogen when W along with the intervening vinylene group carbon atoms forms a 9,10dioxoanthra ring. It is particularly preferred that R8 be methyl when W forms a benzo ring.
R4 groups that are hydrogen, hydroxyl, oxyethanol (-OCH2CH2OH) , oxyacetic acid (-OCH2CO2H) , oxyacetic hydrocarbyl esters such as the beforediscussed C,-C6 alkyl groups such as ethyl oxyacetate (-OCH2CO2CH2CH3) , as well as unsaturated esters such as the allyl, propargyl, 2-butenyl and the like, as well as the benzyl ester and oxyacetic amides constitute particularly preferred embodiments of the invention. Exemplary C1-C6 and benzyl esters that have been prepared; i.e., Compounds 24a-g exhibited activity against MIA PaCa-2 tumor cells.
A pharmaceutically acceptable non-toxic salt of the oxyacetic acid such as sodium, potassium, ammonium, calcium and magnesium is also contemplated.
An oxyacetic acid amide corresponds to the chemical formula -OCH2CONR13R14 wherein R13 is hydrogen (H) or C1-C6 alkyl (as before) and R14 is independently hydrogen, C1-C6 alkyl, phenyl, 1- or 2-napthyl, 1- or 2-anthryl, or a peptide having 1 to about six amino acid residues; or R13 and R14 together with the amido nitrogen atom form a 5- or 6-membered ring as is present in pyrrolidine, piperidine or morpholine. - 14 A particularly contemplated peptide is distamycin, or a derivative thereof as discussed in Taylor et al., Tetrahedron. 40:457 (1984) and Baker et al., J. Am, Chem. Soc.. 111:2700 (1989). Distamycin derivatives are themselves known DNA-cleaving agents.
Indeed, a N-bromoacetyldistamycin adduct of Compound 2 has been prepared. Another particularly preferred peptide is -Ala-Ala-Ala-, [(-Ala-)3].
An R4 group that contains a derivatized 10 oxyacetic acid amide or ester can also include a peptidyl spacer containing zero to about 6 residues such as (-Ala-)3 that links the compound to a monoclonal antibody or an antibody binding site portion thereof, collectively referred to herein as a ”Mab, as is illustrated in relation to Scheme III hereinafter (R or R3). The Mab utilized immunoreacts substantially only with target tumor cells; i.e., is tumor cell specific, and thereby provides further specificity to the drug molecules. Such a Mab-linked fused ring enediyne is one type of chimeric molecule of the invention.
The spacer portion of the compound-Mab construct serves to link the two portions of the molecule together. When there are zero peptide residues present, a lysine epsilon-amino group of the Mab forms the amido bond shown in Scheme III. The spacer peptide chain, when present, is typically comprised of amino acid residues having small side chains such as glycine or alanine, or relatively hydrophilic side chains such as serine, glutamine and aspartic acid. A peptide spacer is typically free of cysteine residues, but otherwise can have substantially any structure that does not interfere with bonding between the two portions of the chimeric compound. A peptide can be prepared by an one of several synthetic methods as are well known. - 15 The Mab portion of the above chimeric construct can constitute an intact antibody molecule of IgG or IgM isotype, in which case, a plurality of compounds can be present per antibody molecule. The binding site portions of an antibody can also be utilized, in which case, at least one compound is linked to the proteinaceous antibody binding site portion.
An antibody binding site portion is that part of an antibody molecule that immunoreacts with an antigen, and is also sometimes referred to as a paratope. Exemplary antibody binding site portions include F(ab), F(ab’), F(ab’)2 and Fv portions of an intact antibody molecule, and can be prepared by well known methods. An intact monoclonal antibody and a portion that includes its antibody combining site portion can be collectively referred to as a paratopecontaining molecule.
Exemplary anti-tumor Mabs are noted in the table below, listed by the name utilized in a publication, along with its deposit accession number at the American Type Culture Collection (ATCC No.), 12301 Parklawn Drive, Rockville, Maryland 20852 U.S.A., and the tumor antigen with which the Mab paratope is reported to react. A citation to a discussion of each Mab and its immunoreactivity is provided by the footnote under the antigen listing. - 16 Exemplary Anti-Tumor Mabs Mab B 3.6 14.8 ATCC No. HB 8890 HB 9118 Antigen GD31 GD22 5 11C64 — GD33 9.2.27 — Condritin sulfate proteoglycan4 R24 — GD35 HT29/26 HB 8247 colon cancer 10 glycoprotein gp 296 HT29/36 HB 8248 colon cancer glycoprotein gp296 CLT85 HB 8240 colon cancer6 F64.5 — mammary carcinoma7 15 R38.1 — pan carcinoma 70Kd protein7 F36/22 HB 8215 human breast carcinoma8 T16 HB 8279 human bladder tumor, 20 glycoprotein gp489 T43 HB 8275 human bladder tumor9 T101 HB 8273 human bladder tumor9 116-NS-19-1 HB 8059 colorectal carcinoma monosialoganglioside10 25 126 HB 8568 GD211 CLH 6 HB 8532 colon cancer12 CLG 479 HB 8241 colon cancer12 19.9 CRL 8019 CEA13 CLNH5 — lung carcinoma14 30 16-88 colon carcinoma151 Cheresch et al., Proc. Natl. Acad. Sci.. USA. ££:5155- 5159 (1985): Ibid. £1:5767-5771 (1984) 352 Cheresch et al. Cancer Res. 44:5112-5118 (1986) - 17 Cheresch et al., J. Cell. Biol.. 102:688(1986) Bumol et al., Proc. Natl. Acad. Sci., USA. 79:1245 5 U.S. Patent No. 4,507,391 6 U.S. Patent No. 4,579,827 10 7 U.S. Patent No. 4,522,918 8 European Patent Application No. 84400420.0, publication No. 0 118 365, published September 12, 1984 15 9 European Patent Application No. 84102517.4, publication No. 0 118 891, published September 19, 1984 20 10 U.S. Patent No. 4,471,057 11 Cheresch et al.. J. Cell. Biol., 102: 688 (1986); U.S. Patent No. 4,675,287 25 12 U.S. Patent No. 4,579,827 13 U.S. Patent No. 4,349,528 14 Patent Application PCT/US83/00781, WO 83/04313 30 15 European Patent Application No. 85300610.4, publication No. 0 151 030, published August 7, 1985 A fused ring enediyne compound of the invention can also be glycosidically linked to a sugar moiety to form a second type chimeric molecule. In such a chimer, the fused ring enediyne compound takes the place of the aglycone as in an antibiotic molecule such as doxorubicin, calicheamicin or esperamicin, with the sugar moiety taking the place of the oligosaccharide portion. Bonding between the fused ring enediyne compound aglycone and oligosaccharide is typically via a hydroxyl group of a spacer group that is itself linked to the fused ring enediyne through a reacted hydroxyl group. A preferred spacer group is an oxyethanol group - 18 that can be an R4 group or can be a substituent of W as is discussed and illustrated hereinafter.
The oligosaccharide portion of the molecule is typically added after the synthesis of the fused ring enediyne compound (aglycone) portion is complete, except for any blocking groups on otherwise reactive functionalities of the aglycone that are typically removed after addition of the oligosaccharide portion.
A sugar moiety is added by standard techniques as are discussed hereinafter.
A glycosidically-linked sugar moiety can be a monosaccharide such as a ribosyl, deoxyribosyl, fucosyl, glucosyl, galactosyl, N-acetylglucosaminyl, N-acetylgalactosaminyl moiety or the more preferred saccharides whose structures are shown below, wherein a wavy line adjacent a bond indicates the position of linkage ΟΜβ - 20 The position of the glycosyl bond to be formed in the sugar moiety used for forming a chimeric compound is typically activated prior to linkage to the fused ring enediyne compound. For example, the 1-position hydroxyl group of an otherwise protected sugar (as with tBuMe2Si or Et3Si groups) is reacted with diethylaminosulfur trifluoride (DAST) in THF and in the presence of 4A molecular sieves at -78°C to form the 1-fluoroderivative. The enediyne having a free hydroxyl group is then reacted with the l-fluro-protected saccharide in the presence of silver perchlorate and stannous chloride to provide a protected desired, typically blocked, chimer molecule.
Similarly, treatment of 1-position hydroxyl of an otherwise protected saccharide with sodium hydride and trichloracetonitrile [Grandler et al., Carbohvdr. res.. 135:203 (1985); Schmidt, Anqew, Chem. Int. Ed., Engl.. 2^:212 (1986)] in methylene chloride at about room temperature provides a 1-a-trichloroacetimidate group to activate the saccharide for coupling with the fused ring enediyne (aglycon) hydroxyl. Coupling is then carried out in boron trifluoride-etherate in methylene chloride to provide the protected desired chimer compound.
Once the aglycone and oligosaccharide are coupled, the protecting groups that are present are removed to provide the desired compound, which is then recovered using standard techniques. Exemplary syntheses are discussed hereinafter.
The 1, 2 or 3 six-membered ring fused rings that along with the depicted vinylene group constitute the structure W are aromatic hydrocarbyl rings. Such rings can thus be benzo, naphtho and anthra rings, using fused ring nomenclature. The anthra (anthracene) derivative rings contemplated here contain 9,10-dioxo - 21 groups (are derivatives of anthraquinone) and are therefore referred to as 9,10-dioxoanthra rings.
Where a benzo, naphtho or 9,10-dioxoanthra ring forms part of the fused ring system, those fused rings are bonded to the remaining fused ring system through the carbon atoms of the 1- and 2-positions or are (a, b). A benzo, naphtho or 9,10-dioxoanthra fused ring portion can also contain one or more substituents at the ring positions remaining for substitution. Those substituent groups are selected from the group consisting of hydroxyl, alkoxy, oxo, acyloxy and halo (chloro, bromo or iodo).
For a benzo ring, one or two substituents can be present at one or two of the remaining positions of the radical. Symmetrical substitution by the same substituent is preferred because of the lessened possibility for isomer formation. When a single substituent is present on a benzo ring, that substituent is referred to as R5, which designation for convenience includes hydrogen. R5 is thus selected from the group consisting of hydrogen (no substituent), alkoxy, benzyloxy, p-nitrobenzyloxy, hydroxyl, acyloxy, oxyethanol, oxyacetic acid, oxyacetic acid hydrocarbyl ester and halo. It is preferred that a hydroxyl group or a group that can form a hydroxyl group intracellularly be present, such that a hydroxyl group be present intracellularly at a position meta to the nitrogen in the adjacent ring. When two substituents are present on a benzo ring, they are referred to as R10 and R11 and are selected from the group consisting of C,-^ alkoxy, benzyloxy, oxo, acyloxy, hydroxyl and halo.
W is more preferably a benzo group that contains a single substituent R5. In one particularly preferred embodiment, R5 is situated in the benzo ring - 22 “ meta or para to the nitrogen atom bonded to R1. That R5 group is more preferably selected from the group consisting of hydroxyl, 0,-C^ alkoxy, benzyloxy, fi-nitrobenzyloxy, 0,-C^ acyloxy, oxyethanol, oxyacetic acid and an oxycacetic hydrocarbyl ester.
When R5 is meta to the above nitrogen atom, it is preferred that the R5 group be an electron releasing group such as hydroxyl or a acyloxy group that can provide a hydroxyl group intracellularly. A acyloxy group is believed to be a pro-drug form of the hydroxyl group that is cleaved intracellularly by an endogenus esterase or the like to provide the hydroxyl group. The presence of such an electron releasing group appears to assist in enhancing the potency of the compound against target tumor cells. It is believed that the enhanced potency is due to enhanced triggering of the epoxide opening and cyclization reactions.
When R5 is para to the above nitrogen atom, it is preferred that the R5 group be an fi-nitrobenzyloxy group, oxyethanol, oxyacetic acid or oxyacetic acid hydrocarbyl ester. Those groups are particularly useful for the preparation of chimeras.
A particularly preferred compound has a structure corresponding to Formula Xlb, hereinafter.
A naphtho ring can have three substituents.
This ring can have a 4-position radical, R5, selected from the group consisting of hydroxyl, alkoxy, benzyloxy, acyloxy and halo, and substituents at the 5- (R10) and 8-positions (R11) that are selected from the group consisting of hydroxyl, C,-^ alkoxy, benzyloxy, acyloxy, oxo and halo radicals. A 9,10-dioxoanthra ring can have three substituents at the 4- (R5) , 5- (R9) and 8-positions (R12) that are independently selected from the group consisting of hydroxyl, alkoxy, benzyloxy, acyloxy and - 23 halo. Thus, R5, R9 and R12 can define the same groups, and all three groups can be written as either R5, R9 or R , but they are shown separately herein.
Exemplary structural formulas for such fused ring compounds are illustrated below by structural Formulas II-IX, wherein each of the R groups is as discussed before. - 25 In addition to the before-stated preference regarding R8 and that bond A be a single bond, several other structural features and substituents are preferred.
Thus, it is preferred that R2 and R3 be hydrogen, and that R6 and R7 be hydrogen. It is also preferred that the fused ring system W together with the depicted vinylene group be substituted benzo, or an unsubstituted benzo, naphtho or 9,10-dioxoanthra ring.
It is further preferred that the fused ring compound contain a total of 3-fused six-membered rings so that W together with the depicted vinylene group forms a benzo ring.
One particularly preferred group of compounds of the invention in which W is an R5-substituted benzo ring corresponds to structural Formula X. wherein A is a double or single bond; R1 is selected from the group consisting of H, C.j-C6 alkyl, phenoxycarbonyl, benzoxycarbonyl, C,-C6 alkoxycarbonyl and 9-fluorenylmethyloxycarbonyl; R2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyloxy C.,—C6 alkyl; - 26 R3 is selected from the group consisting of H and C,-C6 alkoxy; R4 is selected from the group consisting of H, hydroxyl, oxyacetic acid (-OCH2CO2H) , oxyacetic C,-C6 hydrocarbyl or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazylthiocarbonyl and C,-C6 acyloxy; R5 is selected from the group consisting of hydrogen, C,-C6 alkoxy, benzyloxy, o-nitrobenzyloxy, hydroxyl, C,-C6 acyloxy, oxyethanol, oxyacetic acid, oxyacetic acid C,-C6 hydrocarbyl ester and halo; and R6 and R7 are each H or together form with the intervening vinylidine group form a one, two or three fused aromatic ring system, and R8 is methyl or hydrogen.
A still more preferred group of compounds of the invention correspond to structural Formulas XI, XIa and Xlb. xi XIa Xlb wherein R’, R4, R5 and R8 are as previously defined.
Of the compounds corresponding to structural Formula XI, there are further preferences for R1, R4 and R5. These preferences also relate to the previously discussed compounds. - 27 Thus, R1 is most preferably phenoxycarbonyl phenylsulfonylethoxycarbonyl, naphthylsulfonylethoxycarbonyl or hydrogen. R8 is most preferably hydrogen (H) to provide a compound of Formulas XIa or Xlb. R4 is most preferably H, hydroxyl, imidazylthiocarbonyloxy, benzyl oxyacetate and hydrocarbyl oxyacetate such as ethyl oxyacetate. R5 in Formulas XI and XIa is H, but is more preferably hydroxyl, alkoxy, benzyloxy, C,-C6 acyloxy, oxyethanol, oxyacetic acid, oxyacetic acid hydrocarbyl or benzyl ester and a-nitrogenzyloxy as in Formula Xlb. It is noted that an R5 p-nitrobenzyloxy group is not usually used in a pharmaceutical composition discussed hereinafter.
The structural formulas of particularly preferred compounds are shown below, along with compound numbers as utilized herein. In the formulas below and elsewhere herein, Ph = phenyl, Me = methyl, NBnO = fi-nitrobenzyloxy, Naph = naphthyl and tBuC02 = pivaloyl.
Ph- 0-Cx 24c PhS(O)2(CH2)2O MeO II. Pharmaceutical Compositions A compound or chimera of the invention is useful as a DNA cleaving agent, and also as an antimicrobial and a cytoxic (antitumor) agent, as are dynemicin A, calicheamicin, esperamicin and neocarzinostatin. A compound of the invention can also therefore be referred to as an active agent or active ingredient.
DNA cleavage can be assayed using the techniques described hereinafter as well as those described by Mantlo et al., J, Pro, Chem.. 54:2781 (1989); Nicolaou et al., J. Am. Chem. Soc.. 110:7147 (1989); Nicolaou et al., J. Am. Chem. Soc.. 110:7247 (1988) or Zein et al., Science. 240:1198 (1988) and the citations therein. - 30 A compound or chimer of the invention is useful against Gram-positive bacteria such as S. aureus and epidermis. Micrococcus luteus and Bacillus subtillis as is dynemicin A. Such a compound or chimer also exhibits antimicrobial activity against E. coll.
Pseudomonas aeruoinos. Candida albucans and Asperoillis fumiqatus. Activity of a compound of the invention against the above microorganisms can be determined using various well known techniques. See, for example, Konishi et al., J. Antibiotics. XLII:1449 (1989).
Antimicrobial and antitumor assays can also be carried out by techniques described in U.S. Patent No. 4,837,206, whose disclosures are incorporated by reference, as well as by the procedures described hereinafter.
A before-described compound can also be shown to undergo a Bergman cycloaromatization reaction in the presence of benzyl mercaptan, triethylamine and 1,4cyclohexadiene as discussed in Haseltine et al., J, Am.
Chem. Soc.. 111:7638 (1989). This reaction forms a tetracyclic reaction as is formed during DNA cleavage, and can be used as a co-screen to select more active compounds.
A pharmaceutical composition is thus contemplated that contains a before-described compound or chimer of the invention as active agent. A pharmaceutical composition is prepared by any of the methods well known in the art of pharmacy all of which involve bringing into association the active compound and the carrier therefor. For therapeutic use, a compound or chimer of the present invention can be administered in the form of conventional pharmaceutical compositions. Such compositions can be formulated so as to be suitable for oral or parenteral administration, or as suppositories. In these compositions, the agent is - 31 typically dissolved or dispersed in a physiologically tolerable carrier.
A carrier or diluent is a material useful for administering the active compound and must be pharmaceutically acceptable in the sense of being compatible with the other ingredients of the composition and not deleterious to the recipient thereof. As used herein, the phrases physiologically tolerable and pharmaceutically acceptable are used interchangeably and refer to molecular entities and compositions that do not produce an allergic or similar untoward reaction, such as gastric upset, dizziness and the like, when administered to a mammal. The physiologically tolerable carrier can take a wide variety of forms depending upon the preparation desired for administration and the intended route of administration.
As an example of a useful composition, a compound or chimer of the invention (active agent) can be utilized, dissolved or dispersed in a liquid composition such as a sterile suspension or solution, or as isotonic preparation containing suitable preservatives. Particularly well-suited for the present purposes are injectable media constituted by aqueous injectable buffered or unbuffered isotonic and sterile saline or glucose solutions, as well as water alone, or an aqueous ethanol solution. Additional liquid forms in which these compounds or chimers can be incorporated for administration include flavored emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil, peanut oil, and the like, as well as elixirs and similar pharmaceutical vehicles. Exemplary further liquid diluents can be found in Remminoton's Pharmaceutical Sciences. Mack Publishing Co., Easton, PA (1980).
An active agent can also be administered in the form of liposomes. As is known in the art, - 32 liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by monoor multi-lamellar hydrated liquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain stabilizers, preservatives, excipients, and the like in addition to the agent. The preferred lipids are the phospholipids and the phosphatidyl cholines (lecithins), both natural and synthetic.
Methods of forming liposomes are known in the art. See, for example, Prescott, Ed., Methods in cell Biology. Vol. XIV, Academic press, New York, N.Y. (1976), p.33 et seq.
An active agent can also be used in compositions such as tablets or pills, preferably containing a unit dose of the compound or chimer. To this end, the agent (active ingredient) is mixed with conventional tableting ingredients such as corn starch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate, gums, or similar materials as non-toxic, physiologically tolerable carriers. The tablets or pills can be laminated or otherwise compounded to provide unit dosage forms affording prolonged or delayed action.
It should be understood that in addition to the aforementioned carrier ingredients the pharmaceutical formulation described herein can include, as appropriate, one or more additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface active agents, thickeners, lubricants, preservatives (including antioxidants) and the like, and substances included for the purpose of rendering the - 33 formulation isotonic with the blood of the intended recipient.
The tablets or pills can also be provided with an enteric layer in the form of an envelope that serves to resist disintegration in the stomach and permits the active ingredient to pass intact into the duodenum or to be delayed in release. A variety of materials can be used for such enteric layers or coatings, including polymeric acids or mixtures of such acids with such materials as shellac, shellac and cetyl alcohol, cellulose acetate phthalate, and the like. A particularly suitable enteric coating comprises a styrene-maleic acid copolymer together with known materials that contribute to the enteric properties of the coating. Methods for producing enteric coated tablets are described in U.S. Patent 4,079,125 to Sipos, which is herein incorporated by reference.
The term unit dose, as used herein, refers to physically discrete units suitable as unitary dosages for administration to warm blooded animals, each such unit containing a predetermined quantity of the agent calculated to produce the desired therapeutic effect in association with the pharmaceutically acceptable diluent. Examples of suitable unit dosage forms in accord with this invention are tablets, capsules, pills, powder packets, granules, wafers, cachets, teaspoonfuls, dropperfuls, ampules, vials, segregated multiples of any of the foregoing, and the like.
A previously noted preferred or particularly preferred compound or chimer is preferred or particularly preferred for use in a pharmaceutical composition.
A compound or chimer of the invention is present in such a pharmaceutical composition in an amount effective to achieve the desired result. For example, where in vitro DNA cleavage is the desired - 34 result, a compound or chimer of the invention can be utilized in an amount sufficient to provide a concentration of about 1.0 to about 5000 micromolar (μΜ) with a DNA concentration of about 0.02 pq/vl,. As a cytoxic (antitumor) agent, an effective amount of a compound or chimer of the invention is about 0.1 to about 15 mg per kilogram of body weight or an amount sufficient to provide a concentration of about 0.01 to about 50 μg/mL to the bloodstream. A compound or chimer of the invention exhibits antimicrobial activity in a concentration range of about 0.01 mg to about 50 μg/mL. The above concentrations and dosages vary with the particular compound of the invention utilized as well as with the target, e.g., DNA, tumor, microbe, as is well known.
Ill. Methods A compound or chimer of the invention is useful in cleaving DNA, as a cytotoxic agent and also in inhibiting the growth of neoplastic cells, and is utilized in a method for effecting such a result. A compound or chimer of the invention is typically utilized in a before-described composition.
In accordance with such a method, DNA or target cells to be killed or whose growth is to be inhibited are contacted with a composition that contains a compound or chimer of the invention (active ingredient) present in an amount effective or sufficient for such a purpose, as discussed before, dissolved or dispersed in a physiologically tolerable (pharmaceutically acceptable) diluent. That contact is maintained for a time sufficient for the desired result to be obtained; i.e.z DNA cleaved, cells killed or neoplastic cell growth inhibited. - 35 Where the desired result is carried out in vitro, contact is maintained by simply admixing the DNA or target cells with the composition and maintaining them together under the appropriate conditions of temperature and for cell growth to occur, as for control, untreated cells. Thus, a single admixing and contacting is typically sufficient for in vitro purposes.
The above method is also useful in vivo, as 10 where a mammal such as a rodent like a rat, mouse, or rabbit, a farm animal like a horse, cow or goat, or a primate like a monkey, ape or human is treated. Here, contact of a composition and the cells to be killed or whose growth is to be inhibited is achieved by administration of the composition to the mammal by oral, nasal or anal administration or by introduction intravenously, subcutaneously or intraperitoneally.
Thus, contact in vivo is achieved via the blood or lymph systems.
Although a single administration (admixture) and its resulting contact is usually sufficient to maintain the required contact and obtain a desired result in vitro, multiple administrations are typically utilized in vivo. Thus, because of a body's breakdown and excreting pathways, contact between an active ingredient of a composition and the target cells is typically maintained by repeated administration of a compound of the invention over a period of time such as days, weeks or months, or more, depending upon the target cells.
Exemplary methods of the invention for DNA cleavage and inhibition of MIA PaCa-2 human pancreatic carcinoma (ATCC CRL 1420) and MB49 murine bladder carcinoma target cells (obtained from Dr. Lan Bo Chen of the Dana Farber Cancer Institute, Boston, MA) as well as - 36 10 ten other neoplastic cell lines are discussed hereinafter.
IV. Compound Syntheses A compound of the invention can be prepared by a number of routes, several of which are illustrated in the schemes hereinafter. The retrosynthetic plan for these syntheses is illustrated below in Scheme I, with the general forward synthesis shown in Scheme II, thereafter. - 37 Scheme II a, b ; R - Ac 6; R-H 7; R - Si1BuMe2 : Γ 13; R = SiMe3 --br 3;R = H - 38 Briefly, the basic fused 3-, 4- or 5-fused six-membered ring system is first formed.
Following Scheme II for a general synthesis, using the tetrahydro-phenanthridine fused ring system of Compound 4 (W is benzo) as exemplary, an oxygencontaining substituent R4 having an oxygen atom of that group bonding to the 10-position ring carbon atom is formed as Compound 5. Introduction of that oxygencontaining substituent can be accomplished by oxidation as with m-chloroperbenzoic acid (mCPBA), followed by acylation and reflux to rearrange the formed acylated N-oxide to the 10-position (steps a and b) of Compound . The acetyl group is removed to form the alcohol (Compound 6, step c), which is then blocked with a t-butyldimethylsilyl group (SitBuMe2; Compound 7, step d).
An appropriate acetylenic group-containing compound is added adjacent to the nitrogen atom (at the 6-position) as by reaction of an ethynyl Grignard reagent in the presence of an activating moiety that also functions to block the secondary amine so generated, such as phenyl chloroformate to form an R1 substituent of Compound 8 (step e).
The epoxide ring is added next between the 625 and 10-positions by oxidation as with (mCPBA) as in Compound 9 (step f). The formed epoxide ring is on the opposite side of the ring plane from the 6-position acetylenic group, and preferably, the epoxide is in an α-configuration, whereas the acetylenic group is β.
The oxygen-linked R4 group SitBuMe2 is replaced with a hydrogen (step g) and the alcohol so formed is next converted to a ketone, Compound 11 (see also step h, Scheme III). The vinyl acetylene portion of the enediyne-containing ring is added as in Compound 13, when necessary. This step can be carried out by - 39 reacting (Z) l-chloro-4-trimethylsilyl-but-l-en-3-yne (Compound 12) with the ketone Compound 11 in the presence of butylamine, triphenylphosphine and palladium11 acetate (step i) .
Scheme III illustrates that the entire enediyne carbon skeleton can be bonded to the 6-position in a single step, as is discussed hereinafter. Scheme III also illustrates formation of a benzo ring W by reaction of an aniline compound with ethyl cyclohexanone-2-carboxylate. Compound 41 was prepared starting with uj-anisidine (R5 = m-methoxy) , whereas a meta-pivalovl ester (R5 = meta-C5 acyloxy) was prepared from a meta-benzyl ether in preparing Compounds 59a and 59b. Where a R8 methyl group is desired, ethyl 3-methylcyclohexanone-2-carboxylate is utilized.
A derivative of compound such as Compounds 2 or 21 having a hydroxyl group (R5, or R4 of Scheme III) can be prepared following the synthetic route illustrated in Scheme III (R2=H,H) through step j and then Scheme VII, by utilizing meta-(2nitrobenzyloxy)aniline for preparation of a tri-cyclic compound analogous to that formed in step a of Scheme III. The meta-2-nitrobenzyloxy (NBnO) group can be removed after step j of Scheme III to form the meta25 hydroxyl-substituted derivative of a compound such as Compounds 2 or 21 by irradiation with ultraviolet light. A meta-hvdroxvl-substituted derivative of Compound 2, Compound 42, has been so prepared via Compound 43, irradiated, and shown to cause cleavage of double stranded DNA at a 2mM concentration.
After removal of the trimethylsilyl group from the otherwise free (unlinked) acetylenic group (Scheme II, step j), the acetylenic group is inserted into the carbonyl group at position-10 by reaction with a base such as lithium diisopropylamide (LDA) to form a fused - 40 ring compound of the invention where R4 is hydroxyl (OH) (step k) . The R4 group can later be replaced with a hydrogen or derivatized as discussed hereinafter.
As noted before, R6 and R7 are preferably hydrogen (H) . However, R6 and R7 along with the intervening vinylidene group can together form an aromatic mono-, di- or tri-cyclic ring system that can be hydrocarbyl or heterocyclic. When such a ring system is present, the ethylenic bond of the enediynecontaining ring is also one of the unsaturated carbonto-carbon bonds of aromatic ring system, and the entire enediyne carbon skeleton is typically bonded at the 6position (see Scheme III, R2) as a single unit, as is shown in Scheme XI. - 41 Scheme III - 42 Turning more specifically to Scheme III, 2-ethoxycarbonylcyclohexanone is reacted with the aniline (R4 as shown hereinafter), and the reaction product cyclized by treatment with H2SO4. The cyclized material is reduced with lithium aluminum hydride and then air oxidized (step a) to form the tricyclic compound. That compound is oxidized, acetylated and rearranged (steps b and c) to form the acetoxy compound (R=OAc) whose acetyl group is removed to form the alcohol (step d, R=OH) that is then reacted with t-butyldimethylsilyl trifluoromethanesulfonate in the presence of 2,6-lutidine in step e (R=OSilBuMe2) .
The product of step e is reacted first with a chloroformate whose R1 group is shown hereinafter, and then with diacetylide or an aromatic diacetylide ring system compound (R2 as shown hereinafter) blocked with a trimethylsilyl group (TMS) and containing a monoGrignard reagent in step f to form the partially linked macrocyclic ring precursor.
R1 = Me, Ph TMS, PhSOj Naphthyl-SO2xzx\y Anth racy l-SO2Ph3P+\X\ Me3N\^^y η··ο eco CO O) OMe σ OMe H.H - 43 The epoxide ring is formed in step g by reaction with mCPBA. The SitBuMe2 group is removed in step h by reaction with nBuNF, and the resulting alcohol is oxidized with pyridinium chlorochromate in the presence of molecular sieves in step i to form the ketone.
The macrocyclic ring is closed in step j by reaction with lithium diisopropylamide (LDA). The hydroxyl group formed in step j is reacted in step k with an appropriate 2-haloacetic acid derivative (R3 as shown hereinbelow) to form the final product. r3 = ch2cooh CH2CONH-peptide CO (CH2) 2C00Me CH2CONJHPh CH2CONH-Naphthyl CH2CONH-Anthracyl CH2CO2-spacer-Mab spacer-Saccharide R4 = OMe OH OCOMe OCO^u ONBn H Subscripted R groups are used in this scheme to distinguish R groups therein from the superscripted R groups defined elsewhere herein.
The spacer” noted for R3 is a peptide that typically contains zero to about six amino acid residues that links a monoclonal antibody, Mab, to the compound. The R3 spacer linked to an oligosaccharide is typically an oxyethanol or oxyacetic acid group used to form the glycosidic bond to the saccharide, or bond to a paratope-containing molecule. - 44 A vicinal diyne aromatic compound suitable for introduction at the 6-position (based on Compound 4) of a 3—, 4- or 5-fused six-membered ring system can be prepared by alkylation of a vicinal dihalide with trimethylsilylacetylene in the presence of diisopropylamine, dicyanophenylpalladium chloride, triphenylphosphene and cuprous iodide to form the vicinal bis-trimethylsilylacetylene derivative.
Exemplary vicinal dihalo aromatic compounds 10 commercially available from Aldrich Chemical Co. of Milwaukee, WI include 1,2-diiodobenzene, 1.2- dibromobenzene and 1,2-dichlorobenzene. 2.3- Dibromonaphthalene, 2,3-dibromoanthracene and 6,7-dichloroquinoxaline have the following Chemical Abstracts Registry Numbers (R.N.) 13214-70-5, 117820-97-0, and 19853-64-6.
After preparation of the vicinal bistrimethylsilylacetylene derivative, one of the trimethylsilyl groups (TMS) is replaced with a hydrogen atom by reaction with silver nitrate and potassium cyanide. The resulting aromatic diacetylide is then reacted with the fused ring system as described previously.
An appropriate vicinal diacetylide can also be prepared via a vicinal, dihydroxymethyl compound. In one exemplary synthesis, 1,4-dimethoxy-6,7dimethylnaphthalene (R.N. 73661-12-2) is reacted with N-bromosuccinimide (NBS) and azobisisobutyronitrile (AIBN) in a halogenated solvent such as carbon tetrachloride to form the corresponding vicinal dibromomethyl derivative. Reaction of that dibromo compound with hydroxide ion forms the vicinal dihydroxymethyl derivative. Mild oxidation of the dihydroxymethyl compound with pyridinium chlorochromate (PCC) provides the corresponding vicinal dialdehyde. - 45 Reaction of the dialdehyde with triphenylphosphine and carbon tetrabromide, followed by reaction with butyl lithium and then with trimethylsilyl chloride provides the vicinal di-TMS acetylene derivative. Following replacement of one TMS group with hydrogen as discussed before, the aromatic diacetylide is reacted with the fused ring system as was also discussed before.
The above method of synthesis can also be applied to unsubstituted aromatic compounds, such as vicinal dicarboxylic acids, anhydrides or esters. For example, phthalic acid and naphthalene-2,3-dicarboxylic acid are both available from Aldrich Chemical Co.
Either or both can be used to form the corresponding dimethyl esters by reaction with diazomethane.
Reduction of the diesters to vicinal dihydroxymethyl derivatives can be accomplished by reduction using diisobutylaluminum hydride (DIBAL). The resulting dihydroxymethyl compounds are thereafter reacted as described above to form a desired compound.
It is preferred that an aromatic diacetylide contain its two vicinal acetylenic groups symmetrically bonded to the ring system so as to minimize isomer formation. Thus, 2,3-disubstituted-naphthalene, anthracene or quinoxaline compounds are utilized, or a 6,7-disubstituted-quinoxaline, or the like.
An exemplary synthesis for compounds corresponding to structural Formula V is illustrated in Scheme IV, shown below. - 46 Scheme IV NHCO2Md Cl OPMB OH O NHCO2Me li-iii OH O OPMB 27 Ix-xii - 47 Thus, chloronapthazarin, Compound 25, [Banville et al., Can J. Chem.. 52:80 (1974); Savard et al., Tetrahedron. 40:3455 (1984); and Echavarren et al., J, Chem. Res. (3). 364 (1986)] is reacted in step i with diene Compound 26 [Schmidt et al., Synthesis. 958 (1982)] in a Diels-Alder reaction to form the aminoanthraquinone, Compound 27. Reduction of the quinone as with DIBAL in step ii, followed by alkylation with methylene bromide in the presence of cesium fluoride in DMF as step iii provides the O-blocked Compound 28.
Removal of the urethane group with base in step iv, annellation and subsequent reaction as illustrated in Scheme III provides Compounds 29 (steps v-viii) and 30 (steps ix and xii). Compound 30 is then reacted with lithium iodide in pyridine, oxidized with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ), and reacted with pivaloyl chloride (Piv) to form Compound 31 (steps xiii-xv).
Ethylmagnesium bromide is reacted with Compound 31 in the presence of phenyl chloroformate (step xvi). The resulting compound is reacted with mCPBA to form the epoxide (step xvii). The TBS group is removed with nBu4NF to form the alcohol (step xviii) that is then oxidized with Jones reagent (step xix) to form the corresponding ketone. That ketone is reacted with (Z)-l-chloro-4-trimethylsilylbut-l-en-3-yne, palladium0, Cul and butylamine to form Compound 32 (step xx). Compound 32 is reacted with silver nitrate and potassium cyanide (step xxi), LDA (step xxii), thiocarbonyldiimidazole (step xxiii), tri-nbutylstannane and AIBN (step xxiv), and then hydroxide ion (step xxv) to form Compound 33.
For preparation of a compound corresponding to structural Formula IX, 1-aminoanthraquinone (Aldrich - 48 Chemical Co.) can be used as a starting material. Here, the amino group is blocked as with a t-Boc group, the quinone function is reduced as with DIBAL and the resulting phenolic hydroxyl groups are blocked with pivaloyl chloride.
The t-Boc group is then removed as by reaction with trifluoroacetic acid (TFA) and the aromatic ring is annelated with ethyl cyclohexanone-2-carboxylate, followed by cyclization with sulfuric acid, reduction with lithium aluminum hydride and then air oxidation to reform the quinoid structure as the pivaloyl groups are lost during the prior reactions.
The above reactions form the fused ring system. The enediyne macrocycle portion is thereafter added as discussed before.
Where a double bond is desired in the otherwise saturated six-membered ring as is shown in structure Formulas VI, VII, VIII and IX, that functionality can be added as follows. The fused ring system and epoxide are formed, one of the acetylenic linkages is made, the amine blocked and the ketone is formed, all as discussed previously. Exemplary compounds of the required structure are Compounds 13 and 32 shown in Scheme II and IV. The compound is then oxidized to introduce hydroxyl group a (position 9 of Compound 13) to the ketone at position 10 of Compound 13. That hydroxyl group is then blocked as with triethylsilyl (TES or Et3Si) chloride and the macrocyclic enediyne ring is closed. The hydroxyl group resulting from the ring closure is either removed as discussed before or blocked with a group that is not removed by removal of the TES group.
The TES group is removed and the resulting hydroxyl group is oxidized to a ketone as by Swern oxidation. That ketone is then reacted with LDA and - 49 methyl chloroformate to form a carboxy enol whose hydroxyl group can be methylated with diazomethane. Subsequent reaction with hydroxide ion and neutralization provides the unsaturated methoxy carboxylic shown in structural Formulas VI, VII, VIII and IX.
For a compound of structural Formula VI, where the R8 methyl group is present, that methyl group is in the ^-configuration. Here, the ketone formed by the above Swern oxidation is reacted with LDA, phenylselenylbromide and hydrogen peroxide to form an enone. That enone is reduced with copper hydride, which attacks from the α-face to provide the ^-stereochemistry for the R8 methyl group. The reduced enone is then reacted as above to provide the double bond and R2 and R3 groups.
A compound of the general formula of Compound = a) H; b) Methyl; c) Ethyl; d) Iso-propyl; e) Allyl; f) Propargyl; g) Benzyl. can be prepared by reaction of an appropriate 2-haloacetic acid (Compound 24a) or 2-haloacetate ester - 50 (Compounds 24b-g) with Compound 2 in the presence of a base such as cesium carbonate (Cs2CO3) and a crown ether such as 18-crown-6. An exemplary synthesis of Compound 24c is provided hereinafter. A compound wherein R4 is a C1-C6 alkoxy group can be similarly prepared from Compound 2 by alkylation with a C,-C6 halo derivative such as iodo or a triflate derivative in the presence of Cs2CO3.
Removal of the carbamate group from the 10 nitrogen atom of a compound such as Compound 2 to form a free amine-containing compound such as Compound 40 is achieved by reaction with lithium aluminum hydride reduction. Variants in the alcohol portion of a carbamate derivative of a dynemicin analog can be prepared from a phenoxycarbonyl derivative such as Compound 2 by reaction with the replacing alcohol in the presence of the sodium salt of the alcohol as is shown schematically in Figure 15.
V. Results: The key retrosynthetic step that led to the present synthetic strategy is shown in Scheme I, as noted previously. Scheme II outlined the construction of Compound 2 starting from the quinoline derivative Compound 4 [(a) Masamune et al., J, Org. Chem.. 29:681685 (1964); (b) Curran et al., J, Org, Chem.. 49:20632065 (1984); (c) Hollingsworth et al., J, Org, Chem.. 1537-1541 (1948)]. Thus, treatment of Compound 4 with m-chloroperbenzoic acid (mCPBA) in dichloromethane gave the corresponding N-oxide (step a) which underwent regiospecific rearrangement [Boekelheide et al., J. Am.
Chem. Soc.. 76:1286-1291 (1954)] upon heating in acetic anhydride (step b) to give the acetoxy derivative Compound 5 (62 percent overall yield). - 51 Compound 5 was converted to the corresponding silyl ether Compound 7 in 92 percent overall yield by standard methods via hydroxy Compound 6 (steps c and d). Addition of phenyl chloroformate [Comins et al., J, Pro.
Chem.. £5:292-298 (1990)] to a mixture of Compound 7 and ethynylmagnesium bromide at -78°C led to the formation of Compound 8 in 92 percent yield (step e).
Treatment of Compound 8 with mCPBA led to epoxide Compound 9 (85 percent) (step f), which was converted to ketone Compound 11 via alcohol Compound 10 by desilylation (step g) followed by oxidation (step h). Coupling Compound 11 with the vinyl chloride derivative Compound 12 via Pd(0Ac2)-CuI catalysis (step i) followed by AgNOj/KCN treatment (step j) resulted in the formation of the requisite precursor Compound 3 via coupling product Compound 13 (79 percent overall yield). Finally, treatment of Compound 3 with LDA in toluene at -78°C (step k) gave the targeted dynemicin A model Compound 2 (80 percent based on 25 percent recovery of starting material). Compound 2 is also referred to as DY-1 in Figures 10 and 11.
Compound 2 crystallized from ether in colorless prisms, mp 232-235°C dec. X-ray crystallographic analysis (this X-ray crystallographic analysis was carried out by Dr. Raj Chandha, Department of Chemistry, University of California, San Diego) confirmed its structure (ORTEP drawing Oakridge Thermal Ellipsoid Plotter) and revealed some interesting structural features.
The acetylenic moieties are bent from linearity with the following angles: C14, 160.4°; C15, 170.8°; C18, 171.6° and C19, 162.0°. The distance between carbons C14 and C19 (cd distance) [Nicolaou et al., J. Am, Chem, Soc.. 110:4866-4868 (1988)] was found to be 3.63A, a value that agrees well with the - 52 calculated one for the MMX minimized structure of Compound 2 (3.63A) and that of the experimentally derived [(a) Konishi et al, J. Am, Chem. Soc.. 112:3715 3716 (1990); (Jo) Konishi et al., J. Antibiot. . 4£:14491452 (1989)] distance in dynemicin A (3.54A). The calculated distance for these acetylenic carbons was found to be 3.40A. See: Semmelhack et al., Tetrahedron Lett.. £1:1521-1522 (1990). [The MMX87 force field in computer programs MMX and PCMODEL from Serena Software, P.O. Box 3076, Bloomington, IN 47402-3076 was used.] Scheme V outlines a cascade of novel transformations of model system Compound 2. - 53 Scheme V 2: R = H 2a: R s Ac 14:X=0H;R = H 14a : X = OH; R = Ac 14b : X = Cl; R = H I Bergman Cyclization - 54 Thus, upon treatment with p-toluenesulfonic acid (TsOH-H2O) in benzene-1,4-cyclohexadiene (3:1, 0.05 M) at 25°C for 24 hours, Compound 2 was converted to Compound 17 in 82 percent yield, presumably via intermediates 14 and 15. This transformation (2-*17) was also carried out using 1.0 equivalent of TsOH-H2O and 50 equivalents of Et3SiH in benzene at 25°C (24 hours, 85 percent).
For a study using EtjSiH and a number of other 10 hydrogen donors to trap C-centered radicals, see: Newcomb et al., J. Am. Chem. Soc.. 108. 4132-4134 (1986). Compound 17 derived from this reaction with Et3SiH was contaminated with about 5 percent of an, as yet, unidentified product (detected by 1H NMR spectroscopy).
Thus, protonation of the epoxide group in Compound 2 initiates formation of triol Compound 14 which undergoes spontaneous Bergman cyclization [(a) Bergman, Acc. Chem. Res.. 6:25-31 (1973); Jones et al., J. Am. Chem. Soc. . 24.:660-661 (1972); Lockhart et al., J. Am. Chem. Soc.. 103:4091-4096; (b) Darby et al., J. Chem. Soc. Chem, Commun.. 1516-1517 (1971); (c) Wong et al., Tetrahedron Lett.. 21:217-220 (1980)] to form a benzenoid diradical which is, in turn, rapidly trapped by the hydrogen donor present to furnish cyclized product Compounds 15, 15a, or 15b. Under the reaction conditions, triol Compound 15 apparently undergoes a pinacol-type rearrangement leading to the observed final product Compound 17. The structure of Compound 17 was supported by its spectroscopic data and was confirmed by X-ray crystallographic analysis.
Furthermore, it was found that trimethylsilyl trifluoromethylsulfonate (TMSOTf) in the presence of Et3SiH induces the same transformation (2-+17) , (Scheme V) at -78°C in less than 5 minutes (78 percent yield), - 55 suggesting a very low energy of activation for the cyclization process. The rather dramatic shortening of the cd distance in going from epoxide Compound 2 (cd= 3.63A, X-ray and MMX) to triol Compound 14a (cd= 3.19A, MMX) is noteworthy. For comparison with other similar enediyne cyclizations and calculations, see: (1) Nicolaou et al, J, Am. Chem, Soc.. 110:4866-4868 (1988); (b) Nicolaou et al., J, Am, Chem. Soc,. 110:7247-7248 (1988); (c) Hazeltine et al., J. Am. Chem. Soc.. 111:7638-7640 (1989); (d) for similar stabilization of enediynes via cobalt complexation, see: Magnus et al., J. Am. Chem. Soc.. 110:1626-1628 (1988) and Magnus et al., J, Am, Chem. Soc.. HQ:6921-6923 (1988); (e) Semmelhack et al., Tetrahedron Lett.. 32:1521-1522 (1990); (f) Snyder et al J. Am, Chem. Soc.. 111:76307632 (1989); (g) Magnus et al., Tetrahedron Lett.. 30:1905-1906 (1989).
In an attempt to prevent the pinacol rearrangement of triol Compound 15, the acetate derivative Compound 2a was prepared from Compound 2 [acetic anhydride, 4-dimethylaminopyridine (DMAP), 84 percent], and was subjected to the epoxide opening and cyclization reaction conditions as described above. Indeed, the acetate diol Compound 15a was obtained (84 percent yield) as the final product of this cascade starting with Compound 2a and using TsOH-H2O as the initiator (presumably via intermediate Compound 14a).
The use of anhydrous HCI in CH2C12 in the presence of Et3SiH (Scheme V hereinbefore) also resulted in triggering of the cyclization cascade leading from Compound 2 to Compound 15b (85 percent yield) presumably via the intermediacy of Compound 14b (cd= 3.145 A, MMX).
The same conversion (2-*15b) was also effected by the use of 3.0 equivalents of MgCl2 and 50 equivalents of Et3SiH in CH2C12 at 25°C (12 hours, 87 percent) or 1.2 - 56 equivalents of TiCl4 and 50 equivalents of Et3SiH in CH2C12 at -78°C (0.5 hour, 60 percent).
Thus, only Compound 15 underwent the further pinacol-type rearrangement to form Compound 17.
These cyclizations are analogous to those observed for dynemicin A. [(a) Konishi et al., J.
Am.Chem. Soc.. 112:3715-3716 (1990)? (b) Konishi et al., J. Antibiot.. £2:1449-1452 (1989)? (c) Sugiura et al., Proc, Natl, Acad. Sci. USA. 87:3831-3835 (1990)].
An alternate mode of triggering the cyclization of Compound 2 based on cobalt complexation of the acetylenes was devised. This triggering cyclization is illustrated in Scheme VI, below. This pathway was designed so as to prevent the acetylenes from spontaneously cyclizing upon epoxide opening and thus allow the isolation of the postulated intermediate cis-diol. 19a - 58 Thus, reaction of Compound 2 with Co2(CO)8 (2.2 equivalents) resulted in the formation of the dicobalt complex Compound 18 (step a) in 96 percent yield. Use of one equivalent of Co2(CO)8 resulted in the formation of a monocobalt complex in addition to dicobalt derivative Compound 18 and starting material Compound 2. [For similar stabilization of enediynes via cobalt complexation, see: Magnus et al., J. Am, Chem. Soc.. 110:1626-1628 (1988); and Magnux et al., J, Am. chem. SOC.. 110:6921-6923 (1988)].
Treatment of Compound 18 with trifluoroacetic acid in CH2C12 (zero degrees C) followed by aqueous workup led to the formation of the stable cis opening product Compound 19 (step b; 92 percent yield). Upon exposure of Compound 19 to ferric nitrate, or trimethylamine N-oxide in CH2C12 in the presence, or absence, of Et3SiH at 25°C, the cyclized product Compound 17 was obtained in 85-92 percent yield via liberation of the acetylenic groups to afford Compound 14 followed by spontaneous and sequential generation of Compounds 15 and 17 as shown in Schemes V and VI. The same study [reaction with Fe(NO3)3] carried out in CD2C12 resulted in the incorporation of two deuterium atoms in Compound 17 confirming methylene chloride as an effective hydrogen atom donor in these aromatization studies.
To obtain a closer model to dynemicin A, the tertiary hydroxy group in Compound 2 was removed to form Compound 21 as shown in Scheme VII below.
Scheme VII 23: OH 23a: Cl 22: X=OH 22a: X=CI - 60 Thus, reaction of Compound 2 with thiocarbonyldiimidazole in the presence of DMAP resulted in the formation of Compound 20 in 95 percent yield (step a). Compound 20, upon treatment with nBu3SnH in the presence of a catalytic amount of AIBN (toluene, 75°C), led to the desired Compound 21 (step b; 72 percent yield). This model system Compound 21 also underwent smooth cyclization to polycycles Compounds 23 (86 percent) and 23a (82 percent) upon suitable triggering, (as summarized in Scheme VII).
An ORTEP drawing of dynemicin A model Compound (mp 251.2 52°C dec, from ether - petroleum ether) as determined by X-ray crystallographic analysis was prepared. The following angles revealed considerable deviation of the acetylenic groupings from their preferred linear arrangement: C17-C18-C19 = 170.2°; C9-C19-C18 = 162.0°; C14-C15-C16 = 170.1°; and C13-C14-C15 = 163.7°. The distance between carbons C14 and C19 (cd distance) was found to be 3.59A, which agrees well with the values derived for the MMX minimized structure of Compound 21 (3.59A) and from the X-ray crystallographic analysis of dynemicin A (3.54A). [Konishi et al., J, Am, Chem, Soc.. 112:3715-3716 (1990)]. Again, the considerable shortening of the cd distance is noted in going from 9 to the cis diols 10 (cd= 3.21A, MMX) and 10a (cd= 3.19A, MMX).
In order to allow for the generation of the parent enediyne system Compound 40, Compound 45 was designed and synthesized from Compound 21 as shown in Scheme VIII, below. - 61 Scheme VIII : X = OPh; R = H : X = SPh; R = H : X = OH; R = OMe Thus, Compounds 21 and 46 were separately reacted with ten equivalents of 2-phenylthioethanol [PhS(CH2)2OH] in acetonitrile for 12 hours in the presence of three equivalents of Cs2CO3 and 0.5 equivalents 18-crown-6 in step a to form the corresponding phenylthioethoxy Compounds 21a and 46a, respectively. The products of that reaction were then individually reacted with 2.5 equivalents of mCBPA in CH2C12 at 0-25°C to provide Compounds 45 (85 percent overall) and 47 (82 percent overall) as step b. When step b is carried out with one equivalent of mCBPA, the corresponding sulfoxides, Compounds 21b and 46b are prepared.
To prepare Compound 40 that was too labile for isolation, Compound 45 was reacted with an excess of Cs2CO3 and 0.5 equivalents of 18-crown-6 in a dioxane:1,4-cyclohexadiene (4:1) solution for one hour at 25°C as step c. Compound 47 was reacted with 1.2 equivalents of l,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in benzene at 5°C for one hour to provide a 97 percent yield of Compound 48 as step c.
Freshly prepared Compound 40 was reacted with either phenol (i, PhOH) or thiophenol (ii, PhSH) using two equivalents of either nucleophile at 25°C for two hours to provide Compounds 49 (25 percent yield) or 50 (33 percent yield, respectively, as step d. The reactivity of Compound 40 and its ability to cleave DNA add credibility to the notion of a pathway including epoxide ring opening and the intermediacy of an iminoquinone methide species in the mode of action of dynemicin A, at least as a partial mechanism.
Interestingly, the methoxy derivative, Compound 48 proved to be quite stable under basic or neutral conditions. Treatment of Compound 48 with 0.5 equivalents of p-toluenesulfonic acid-H2O (step d iii, - 63 10 TSOH) in dioxane:water:1,4-cyclohexadiene (4:1:1) at 60°C for ten minutes provided Compound 51 (20 percent yield).
An X-ray crystallographic analysis of Compound 48 confirmed its molecular structure and revealed a number of interesting parameters including a cd distance of 3.63A [Calcd. cd=3.6lA, MMX] and the non-linearity of the acetylenic groupings [angles at acetylenic carbons: C-14, 163.3°; C-15, 173.0°; C-18, 169.3°; C-19, 160.5°].
Enediyne model system Compound 43 (Scheme IX) was designed for its potential to generate species 42 under photolytic, neutral conditions. Following the strategy developed earlier for the synthesis of Compound 21, Compound 43 was constructed in good overall yield. Reactions of Compound 43 are shown in Scheme IX.
Scheme IX la· i) EtOH ii) EtSH iii) n-PrNH2 44a: R = PhO; Nu = EtO + 54: R = PhO 44b: R = PhO; Nu = EtS 44c: R = Nu s NHn-Pr - 65 Irradiation in step a of Compound 43 in THFH2O (10:1) for 40 minutes [Hanover mercury lamp, pyrex filter] at ice-cooling temperature resulted in clean conversion to Compound 42 as observed by TLC and 1H NMR spectroscopy (THF-d8: D2O 10:1, 300 MHz). Attempted isolation of Compound 42 led to decomposition, whereas treatment of crude Compound 42 in a pH 8.0 buffer-THF solution containing either ethanol (EtOH), mercaptoenthanol (EtSH) or n-propylamine (nPrNH2) as 10 nucleophiles (Nu) at 25°C under argon atmosphere for 1.5 hours provided a mixture of Compounds 44a and 54 (31 percent yield), 44b (34 percent yield), or 44c (46 percent yield), respectively, as step b.
Noteworthy was the isolation of Compound 54 15 (Scheme IX) in about 5-10 percent yield from the reaction of 42 with ethanol, in air, along with Compound 44a (33 percent yield), as a sensitive but stable molecule under neutral conditions. The isolation of Compound 54 provides strong evidence for the intermediacy of quinone methide Compound 52, [a) Dyall et al., J, Am. Chem. Soc.. ££:2196 (1972); b) Zanarotti, Tetrahedron Lett.. £3:3815 (1982); c) Zanarotti, J. Org. Chem.. 50:941 (1985); d) Angle et al., J. Am, Chem, Soc.. 111:1136 (1989); e) Angle et al., Tetrahedron Lett.. 301193 (1989); f) Crescenzi et al., ibid 31:6095 (1990); g) Barton et al., ibid ££:8043 (1990); h) Angle et al., ibid 112:4524 (1990)], trapping of which with molecular oxygen would provide Compound 54 as is shown in Scheme X, below. - 66 Scheme X PhOC(O).
THF-buffer (1:1) 25 °C /70 h OR-i 42: R1 s H 55: Ri = Me PhOCfOK 52: Ri = H 56: Ri = Me O2 Remarkably, treatment of Compound 55 under similar conditions (THF-pH 9.0 buffer in air) resulted in the isolation of Compounds 58 and 62 in 32 percent and 25 percent yields, respectively, as stable molecules. Quinone methide intermediates have been implicated in the mode of action of anthracycline antibiotics [for recent postulated quinone methide intermediates in the area of anthracycline antibiotics, see: a) Boldt et al., J. Org. Chem.. £2:2146 (1987); b) Gaudiano et al., J. Org. Chem.. ££:5090 (1989); c) Egholm et al., J. Am. Chem. Soc.. 111:8291 (1989)? d) Ramakrishnan et al., J, Med Chem.. 29:1215 (1986); e) Boldt et al., J. Am. Chem. Soc.. 111:2283 (1989)? f) Gaudiano et al., J. Am, Chem, Soc.. 112:9423 (1990); g) Karabelas et al., J. Am. Chem. Soc.. 112:5372 (1990)? h) Gaudiano et al., J. Am. Chem, Soc.. 112:6704 (1990)] and dynemicin A.
The pivaloate ester Compounds 59a and 59b were also synthesized according to the previously discussed general strategy for their potential to liberate phenolic species of type of Compound 42 (Scheme IX), thus presenting yet another triggering mechanism to initiate the dynemicin A-type cascade. Indeed, upon exposure to four equivalents of LiOH in ethanol:water (3:1) at 25°C for 4-6 hours, Compounds 59a and 59b were smoothly converted to products 60a (56 percent) and 60b (42 percent), respectively, presumably via a sequence involving concomitant carbamate exchange [EtO- for PhO-]. 60a: R = OH 60b: R = H The methoxy Compound 41 was also synthesized and exhibited reasonable stability under neutral and basic conditions. As expected, however, this compound cyclized rapidly under acidic conditions. For example, upon treatment with TsOH«HzO in benzene:1,4cyclohexadiene (1:1) at 25°C for one hour, Compound 41 afforded the aromatized product Compound 61 (32 percent yield). - 69 Treatment of Compound 41 as per steps a and b of Scheme V yields the corresponding methoxyphenyl derivative Compound 41a having a hydrogen in place of the hydroxyl of Compound 41. Treatment of Compound 41a with 2-phenylthioethanol, 2-a-naphthylthioethanol or 2-β-naphthylthioethanol under basic conditions as discussed in regard to Scheme VIII, followed by oxidation led to Compounds 41b, 41c and 4Id, respectively.
The synthesis of Compounds 70 and 80 proceeded as summarized in Scheme XI, shown below. - 70 Scheme XI - 71 Thus, coupling of the readily available Compounds 11 [Nicolaou et al., J, Am. Chem. Soc.. 112:7416 (1990); Nicolaou et al., J. Am. Chem. Soc.. 113:3106 (1991)] and 71 using palladium (0)-copper(1) catalysis afforded product Compound 72 (55 percent yield) as step a. Desilylation of Compound 72 with lithium hydroxide in step b followed by base-induced (lithium diisopropylamide; LDA) ring closure led to Compound 74 via 73 (75 percent overall yield) in step c.
Conversion of Compound 74 to the thionoimidazolide Compound 75 (84 percent based on 67 percent conversion of staring material) as discussed elsewhere herein, followed by deoxygenation with tri-n-butylstannane (nBu3SnH) in step e resulted in the formation of 76 (94 percent). Exchange of the phenoxy (PhO) group of Compound 76 with 2-phenylthioethoxy (PhSCH2CH2O) took place smoothly under basic conditions (two equivalents of PhSCH2CH2ONa, THF) leading to Compound 77 (92 percent yield) in step f, from which the sulfone Compound 70 was generated by oxidation using 2.5 equivalents mCPBA (81 percent yield) in step g.
Similar chemistry employing the naphthalene ditriflate Compound 81 led from Compound 11 to arenediyne Compounds 85-80 via intermediate Compounds 82-84 in comparable yields as depicted in Scheme XI.
Step h utilized acetonitrile as a solvent and a one hour reaction time as compared with step a of the scheme that used benzene as solvent and 3.5 hours of reaction to obtain yields of 55 and 56 percent, respectively. Step i utilized five equivalents of trimethylsilylacetylene, 0.05 equivalents of Pd(PPh3)4, 0.2 equivalents of Cul and two equivalents of triethylamine in acetonitrile (as were present in steps a and b) with a reaction time of 20 hours at 25°C to provide Compound 82 in 76 percent yield. Steps c-g of both reactions were identical. - 72 10 Reaction of Compounds 77 or 88 with one equivalent each of mCPBA leads to preparation of the corresponding sulfoxides, Compounds 77a and 88a.
The free amine Compounds, 76a and 87a, shown below, corresponding to Compounds 76 and 87 were prepared from their corresponding phenylsulfonylethyl carbamates 70 and 80 under basic conditions. Those compounds were both stable at 25°C, whereas Compound 40 decomposed at that temperature.
Treatment of Compounds 76a and 87a with silica gel in benzene initiated epoxide opening to form the corresponding diols 76b and 87b, respectively. Diol Compound 76b cyclized spontaneously at 25°C in the presence of 1,4-cyclohexadiene to form the cycloaromatized diol, Compound 76c. In contrast to Compound 76b, diol Compound 87b was stable in the presence of 1,4-cyclohexadiene, but cycloaromatized at elevated temperature (65°C, two hours) to form Compound 87c. 87a The cycloaromatization of enediyne Compounds 76, 70, 87 and 80 was then studied in order to determine the precise structural and spectroscopic changes taking - 73 place. Thus, whereas cycloaromatization of Compound 76 (about 0.02M solution) under acid conditions [1.2 equivalents of TsOH.H2O, benzene-cyclohexdiene (4:1), 25°C, four hours] produced smoothly the corresponding naphthalene derivative (78 percent) no dramatic changes in the UV and fluorescent spectra were observed for the starting arenediyne and cycloaromatized product.
In contrast, however, similar acid-induced Bergman cycloaromatization of the naphthalene enediyne Compound 87 furnished the epoxy-containing anthracene derivative Compound 89 (49 percent) that exhibited, as expected, strong and characteristic UV and fluorescence profiles that were distinct from those of the starting arenediyne Compound 87 [UV (EtOH), 87^^ (log e) 304 (3.47, 294 (4.01), 284 (4.26), 267-240 (4.53-4.55), 214 (4.50) nm; 89^^ (log e) 390 (3.74), 369 (3.78), 351 (3.66), 333 (3.45), 318 (3.20), 267-244 (4.43-4.46), 214 (4.43) nm. Fluorescence (EtOH, 1 μΜ, excitation at 260 nm, Compound 87:λΜχ 435, 412, 393, 374, 357 nm; 89 520, 466, 442, 413, 392 nm].
Attempted cycloaromatization of Compounds 70 and 80 under a variety of basic conditions led to decomposition, presumably via the in situ generated free amines and diradical species, whereas acid treatment resulted in the formation of epoxy-opened (dihydroxy) Compounds 78 and 89a albeit in low yields (20 percent and 15 percent, respectively). Interestingly, both Compounds 70 and 80 exhibited DNA cleaving properties under basic conditions (supercoiled 9174 DNA, pH 9.0) and potent anticancer activity against a variety of cell lines as discussed hereinafter.
Saccharide-Containing Chimeras Chimeric compounds that include both a fused ring enediyne as the aglycone and a before-discussed - 74 mono- or oligosaccharide as the oligosaccharide portion is also contemplated, as noted earlier. The previously depicted saccharides are related to the calicheamicin oligosaccharide.
The before-depicted saccharides correspond to the calicheamicin oligosaccharide (Structures F and G), the oxime precursor thereto (Structures D and E), and fragments thereof (Structures A-C). More specifically, the disaccharide Structure λ corresponds to the calicheamicin A and E rings with the hydroxylamine link to a B ring analog. The monosaccharide Structure B corresponds to the A ring alone with the hydroxylamine1inked B ring analog. The trisaccharide thiobenzoate Structure C corresponds to rings A, E and B, and a C ring analog. The 5-ring Structure D corresponds to the FMOC-blocked oxime precursor to the complete calicheamicin oligosaccharide, whereas 5-ring Structure E is the FMOC-deblocked version thereof. Structures F and G are the complete calicheamicin oligosaccharides that are epimeric about the 4-position of the A ring hydroxylamine linkage, with Structure F having the native calicheamicin oligosaccharide stereochemistry. These saccharides are discussed in more detail hereinafter.
Inasmuch as the previously depicted saccharides of the calicheamicin oligosaccharide are derivatives of known compounds, as are their suitably protected precursors, their complete syntheses need not be discussed in complete detail herein. Those syntheses are described in Nicolaou et al., J. Am. Chem. Soc.. 112:4085-4086 (1990); Nicolaou et al., Ibid.. 112:81938195 (1990); Nicolaou et al., J. Chem, Soc.. Chem, Commun.. 1275-1277 (1990) as well as in U.S. Patent Application Serial No. 07/520,245 filed May 7, 1990 and Serial No. 07/695,251 filed May 3, 1991, all of whose - 75 disclosures are incorporated by reference herein. Nevertheless, the saccharides used herein differ somewhat from the reported saccharides, so their syntheses will be discussed, at least in pertinent part herein below.
The disaccharide-linked hydroxylamine compound is prepared in a manner analogous to that of Compound 12 of Nicolaou et al., J. Am. Chem. Soc.. 112:8193-8195 (1990), except that an fi-nitrobenzyl (shown as NBnO or ONBn in the schemes) glycoside is utilized instead of the methyl glycoside precursor, Compound 9 of that paper. The synthesis for the disaccharide is illustrated in Schemes XII and XIII, and is discussed below.
Scheme XII Thus, D-fucose Compound 90 was peracetylated in step a to form tetraacetate Compound 91 which was converted to the anomeric bromide Compound 92 in step b, and glycosylated with fi-nitrobenzyl alcohol to afford Compound 93 in step c (63 percent overall yield). Deacetylation of Compound 93 in step d led to Compound 94, which reacted selectively with carbonyl diimidazole in step e to afford the requisite ring A intermediate 95 in 86 percent overall yield. 107 - 77 Turning to Scheme XIII, intermediate Compound 95 was then coupled [Mukaiyama et al., Chem, Lett.. 431 (1981); Nicolaou et al., J, Am, Chem. Soc.. 106:4159 (1984)] to glycosyl fluoride Compound 96 (Compound 8 of the above paper; Me-methyl) with AgC104-SnCl2 catalyst in step a, leading stereoselectively to disaccharide Compound 97 as the major anomer (80 percent yield, about 5:1 ratio of anomers). Chromatographic purification of Compound 97 with removal of the carbonate protecting group (NaH-HOCH2CH2OH, 90 percent) in step b to form Compound 98, and treatment in step c with nBu2SnO-Br2 [David et al., J, Chem, Soc. Perkin Trans 1. 1568 (1979)] led to hydroxyketone Compound 99 (65 percent yield plus 17 percent Compound 98) via intermediate Compound 98.
Oxime formation in step d with O-benzyl hydroxylamine under acid conditions led to Compound 100 (90 percent, single geometrical isomer of unassigned stereochemistry; Ph=phenyl) which was silylated in step e under standard conditions to furnish Compound 101 (90 percent). Photolytic cleavage [Zenhavi et al., J. Pro. Chem.. 37:2281 (1972); Zenhavi et al., ibid. 17:2285 (1972); Ohtsuka et al·., J, Am, Chem. Soc.. 100:8210 (1978); Pillai, Synthesis. 1 (1980)] of the o-nitrobenzyl group from Compound 101 (THF-H2O, 15 minutes) produced lactol Compound 102 in 95 percent yield in step f. Treatment of Compound 102 with NaH-Cl3CCsN [Grandler et al., Carbohvdr, Res.. 135:203 (1985); Schmidt, Anqew Chem, Int. Ed., Engl.. 15:212 (1986)] in CH2C12 for two hours at 25°C in step g resulted in the formation of the a-trichloroacetimidate Compound 103 in 98 percent yield. Reaction of benzyl alcohol (2.0 equivalents) with trichloroacetimidate Compound 103 under the Schmidt conditions [Grandler et al., Carbohvdr. Res.. 135:203 (1985); Schmidt, Angew - 78 Chem. Int. Ed., Engl.. 2£:212 (1986)] [BF3-Et2O, CH2C12, -60 -+ -30°C] resulted in stereoselective formation of the /3-glycoside Compound 104 (79 percent yield) together with its anomer (16 percent, separated chromatographical ly) [1H NMR, 500MHz, C6D6, 104: J12=6.5 Hz, epi-Compound 104: J12= 2.4 Hz].
On the other hand, treatment of lactol Compound 102 with DAST in step g' led to the glycosyl fluoride Compound 102a in 90 percent yield (about 1:1 anomeric mixture). Reaction of Compound 102a with benzyl alcohol in step h' in the presence of silver silicate [Paulsen et al., Chem. Ber.. 114:3102 (1981)] - SnCl2 resulted in the formation of the jS-glycoside Compound 104 and its anomer in 85 percent (about 1:1 anomeric mixture).
Generation of intermediate Compound 106 via Compound 105 proceeded smoothly under standard deprotection conditions in steps i and j. Finally, exposure of Compound 106 to Ph2SiH2 in the presence of Ti(O’Pr)4 in step k resulted in the formation of the desired target Compound 107 as the only detectable product (92 percent yield). Interestingly, reduction of Compound 106 with NaCNBH3-H led predominantly to the 4-epimer of Compound 107 (90 percent yield). The stereochemical assignments of Compound 107 and epi-107 at C-4 were based on 1H NMR coupling constants [’h NMR, 500MHz, C6D6, 107: J34=9.5, J4>5=9.5 Hz; epi-107: J3<4=1.9 Hz, J4 5=1.5 Hz] .
The hydroxylamine linked A ring derivative (Structure B) can be prepared starting with Compound 9 of Nicolaou et al., J. Am. Chem. Soc.. 112:8193-8195 (1990). There, the 2-hydroxyl is blocked with a t-butyldimethylsilyl (lBuMe2Si) group as before, and the carbonate group removed by reaction of sodium hydride in ethylene glycol-THF at room temperature. The keto group - 79 10 can be prepared by oxidation with dibutylstannic oxide (nBu2SnO) in methanol at 65°. The 3-position hydroxyl is similarly blocked with a *BuMe2Si group, and the oxime formed as above.
The trisaccharide plus C ring analog (Structure C) can be readily prepared from Compound 19 of Nicolaou et al., J. Am. Chem. Soc.. 112:8193-8195 (1990). Thus, that Compound 19 is reacted with benzoyl chloride in the presence of triethylamine and a catalytic amount of DMAP in methylene chloride to provide the blocked oxime-containing trisaccharide.
The use of Compounds 2 and 103 in preparing an exemplary chimera is illustrated in Scheme XIV, below, and discussed hereinafter.
PhO N Scheme XIV a|—2: R = H ‘-►24c: R = CH2COOEt . 110: R = CHjCOS CI 111:R = CH2CH2OH PhO N OMe R2 N OPh Mev°y°' MeW*0 PhCH.O-N^V^O^O ΜζΗΟ„2Ο.Ν^Υ^-Ο^Ο^ ‘ PhCH20-N'' H PhO N PhCH2O-N « 11 OR1 Ri s SiEtj, R2 b FMOC Ri = H, Rj = FMOC R, = R2 = H 112b 115b 115a Thus, as shown in Scheme XIV, coupling of Compound 2 with ethyl bromoacetate under basic conditions led to derivative Compound 24c (60 percent yield), which was converted to primary alcohol Compound 111 (80 percent overall yield) by: (i) ester hydrolysis; (ii) 2-pyridyl thiolester formation (collectively step b) and (iii) reduction in step c. Coupling of Compound 111 (1.2 equivalent) with trichloracetimidate Compound 103 under the influence of BF3*Et2O as described before led to the formation of two major products (70 percent, about 1:1 ratio) and two minor products (14 percent, about 1:1 ratio), which were chromatographically separated.
The major isomers were shown to be the diastereomeric /3-glycoside Compounds 112a (Rf=0.12, silica, 20 percent ethyl acetate in petroleum ether) and 112b (Rf-0.10, silica, 20 percent ethyl acetate in petroleum ether) [’h NMR, 500MHz, C6D6, 112a; J12=6.5 Hz; 112b; J, 2=6.5 Hz], whereas the minor isomers were shown to be the α-anomers of Compounds 112a and 112b at C-1 [’h NMR, 500MHz, C6D6, epi-112a, J,2=2.4 Hz: epi-112b, J, 2=2.4 Hz]. Sequential deprotection of Compounds 112a and 112b as described above for Compound 104 led to oxime Compounds 114a and 114b via intermediate Compounds 113a and 113b, respectively.
Finally, reduction of Compounds 114a and 114b under the Ph2SiH2-Ti (OiPr)4 conditions led exclusively to the targeted Compounds 115a and 115b respectively (90 percent yield). The C-4 stereochemistry of Compounds 115a and 115b was again based on the coupling constants J43=9.5 and J4 5=9.5 Hz for the newly installed H-4.
Structures 112a-115a and 112b-115b are interchangeable, since the absolute stereochemistry of the aglycons has not been determined. Physical data for Compounds 115a and 115b are provided hereinafter. - 82 Still further chimeras have been prepared that contain a fused-ring enediyne glycosidically-linked to the complete calicheamicin oligosaccharide or an analog thereof. Exemplary synthetic steps are outlined in Schemes XV and XVI, below. - 83 Scheme XV ?Μθ fmoc Μβγ°γχ γλύ'ν'1Me ο Μβγ°γ% OSiEtj 0SiEt3 OMe Μβ,,,^Ο^^Ο EtaSiO^'v'^OSIEta OMe -^Y^OMe OMe c bC Q 121: X = CH/ N02 122: X = OH 123: X = OCCCI3 II NH O-L-A x—' O | 120 ^I~~A OMe FMOC Me. 0 — -N· ..-γ^ιχζη. 'y^vAs^M OSiEta 'yuMe 0SiEt3 124a Me O Me... ,0^.0 EIjSiO^S^'^’S'E'j 0Me OMe - 84 Thus, a compound such as Compound 111 of Scheme XIV was reacted with phenylthioethanol in the presence of a base as discussed elsewhere to exchange out the phenoxide moiety from the corresponding carbamate. That compound was then oxidized with E-chloroperbenzoic acid to form the corresponding 2-(phenylsulfonyl)ethyl carbamate, Compound 120.
Racemic compound 120 was reacted with Compound 123 as shown in Scheme XV. Compound 123 was prepared from Compound 121 via compound 122, and shown in the scheme and discussed in regard to Scheme XIII as to the preparation of Compound 103. Compound 121 was itself prepared in a manner analogous to that discussed in Nicolaou et al., J, Am. Chem. Soc.. 112;8193-8195 (1990), except that Compound 99 herein was utilized instead of Compound 12 of the published paper, and Et3Si blocking groups were used instead of lBuMe2Si blocking groups that were used in the published paper.
Thus, Compound 121 was irradiated in THF-H2O (9:1/ v/v) at zero degrees C in step a to provide a 95 percent yield of Compound 122. That compound was reacted with a catalytic amount of NaH and trichloroacetonitrile in methylene chloride (1:12, v/v) at 25°C to provide a 98 percent yield of Compound 123 in step b. Compounds 120 and 123 were coupled in step c in benzyl alcohol, BF3-Et2O in methylene chloride at -60° -* -30°C to provide Compound 124 as a mixture of diastereomeric anomers 124a and 124b present as a β- to α-anomer ratio of about 5:1, the /3-anomer being shown as Compound 124a, and the α-anomer, Compound 124b, not being shown.
Reaction of Compounds 124a and 124b with nBuNF using standard conditions removed the triethylsilyl groups. The oxime- and FMOC-containing, hydroxyl deblocked compound that resulted, Compounds 125a and - 85 125b, thus contained the oligosaccharide portion discussed previously as oligosaccharide Structure D. Subsequent reaction with diethylamine under usual conditions removed the FMOC group to form Compounds 126a and 126b. The completely deblocked oxime-containing oligosaccharide portion of Compounds 126a and 126b is the oligosaccharide discussed previously as oligosaccharide Structure E.
Scheme XVI Scheme XVI shows only the oxime-containing ring of Compound 126a, with the remaining portions indicated by the wavy lines. As is shown in Scheme XVI, reduction of Compound 126a with sodium cyanoborohydride in BF3-Et2O at -50°C provided a 65 percent yield of - 86 ~ epimeric Compounds 127a and 127b, that were present in about equal amounts. Those compounds were epimeric at the 4-position of the A ring as indicated by the number 4 and the arrow. The epimeric portions of Compounds 127a and 127b provide the oligosaccharide portions previously identified as oligosaccharide Structures F and O, with only the epimer present in calicheamicin (Structure F) being shown in Scheme XVI.
As prepared, Compounds 125-127 were mixtures 10 of diastereomers. Those diastereomers have been separated, but the absolute configurations of the fusedring enediyne portions are presently unknown, and only one is illutrated, whereas both were shown in Scheme XIV.
Preparation of other chimeras using other appropriate fused ring enediyne aglycons and oligosaccharide portions.
As noted earlier, an R5 group such as that shown in Formula X is preferably a hydroxyl group or a group convertible thereto intracellualarly. The presence of an R5 hydroxyl group also provides an atom (oxygen) that can be used to link a hydroxyl-containing spacer group that itself can be glycosidically linked to a before-described saccharide. A generalized synthesis is illustrated in Scheme VI. A more specific partial synthesis is illustrated in Scheme XVII, below, that was used to prepare Compound 59.
Scheme XVII 133 130 R,R=O, X=OEt Thus, in accordance with Scheme XVII, ethyl cyclohexanone-2-carboxylate, Compound 130 was reacted in step a with 1.2 equivalents of ethylene glycol and 0.1 equivalents of TsOH-H2O in benzene at reflux for ten hours to form Compound 131. Compound 131 was reacted in step b with sodium methoxide-methanol at reflux for eight hours to form Compound 132 in 78 percent yield from Compound 130.
Compound 132 was then reacted in step c with 10 Compound 133 in the presence of 1.2 equivalents of DCC and 0.1 equivalents of DMAP in methylene chloride at 25°C for 14 hours to form Compound 134 in 96 percent yield. Compound 134 was reacted with m-aminophenol in THF at reflux for 96 hours to provide Compound 135 in 87 percent yield in step d. Compound 135 was reacted with benzylbromide, 1.05 equivalents of NaH and 0.1 equivalents of nBu4NI in THF at 25°C in step e to form Compound 136 in 72 percent yield.
Compound 136 was cyclized in step f in 37 percent HCl-THF (1:2.7) at reflux for three hours to provide a mixture of the cyclized product Compounds 137a and 137b in 100 percent yield. Compounds 137a and 137b were formed in about a 4:1 ratio in the order named. Compounds 137a and 137b as a mixture were treated with DIBAL and two equivalents of LiAlH4 in THF at reflux for three hours and then with oxygen and SiO2 at 25°C for 24 hours to form Compound 138 in 50 percent yield.
A similar reaction sequence can be used with p-anisidine in place of the m-aminophenol to form the corresponding methoxy compound. That compound when treated with two equivalents of sodium ethylthiolate in DMF at 160°C, followed by acylation with acetic anhydride and then reaction with sodium methoxide provides the substituted phenol para- to the nitrogen atom. That phenol, when treated as in step e forms the benzyl ether, Compound 139.
Either of Compounds 138 or 139, when treated as in steps a and b of Scheme II, or c-e of Scheme III provides the corresponding benzyloxy Compounds 140a or 140b. Hydrogenation of either of Compounds 140a or 140b using 10 percent Pd/C in ethanol at 25°C provides the corresponding phenol derivatives Compounds 141a and 141b.
Reaction of either phenol with 1.05 equivalents of NaH and mercaptothiazolyl pivolate in THF provides the corresponding pivaloyl esters Compounds 142a and 142b. The pivaloyl ester Compound 142a was prepared as discussed above after a five minute reaction time at 25°C in 99 percent yield.
Similarly, reaction of either of Compounds 141a and 141b with 1.05 eguivalents of NaH and of o-nitrobenzyl bromide and 0.1 equivalents of nBu4NI in THF provides the corresponding photolabile ONBn group and Compounds 143a and 143b. Compound 143a was prepared in 90 percent yield after a one hour reaction time.
Any of Compounds 142a, 142b, 143a or 143b can be used to form a fused-ring enediyne compound of the invention using the steps outlined in the prior reaction schemes, such as Compounds 59a and 59b.
Scheme XVIII OCH2CH2OH e The use of Compound 143b to prepare fused-ring enediyne compounds having a spacer portion in the benzo ring para to the carbamate nitrogen atom is illustrated in Scheme XVIII. Thus, Compound 143b is reacted as discussed elsewhere herein to form fused-ring enediyne Compound 150. Those prior reactions are indicated schematically by the two arrows between Compounds 143b and 150. Compound 150 is a para-hvdroxv analog of the compound formed in step b of Scheme VIII.
Compound 150 is then reacted in step a with 2-bromoethanol and NaH in the THF to form Compound 151. Compound 151 is oxidized in step b as with mCPBA to form Compound 153, whose ethoxyethanol hydroxyl group can be used to form a glysidic link to a saccharide as discussed previously.
Compound 150 can also be reacted with ethyl bromoacetate and cesium carbonate in acetonitrile as in step c to form the corresponding ethyl carboxymethyl derivative. Hydrolysis of that ester with lithium hydroxide in THF-water and neutralization provides the free acid Compound 152 in step d. Oxidation of the free acid as in step b provides Compound 154. The carboxylic acid group of Compound 154 can be used to form a chimera via an ester link to a before-discussed saccharide, or an ester or amide link to a before-discussed monoclonal antibody.
The results of an exemplary DNA-cleaving study using Compound 40 in a method of the invention are illustrated in Figure 1. Other compounds such as Compound 41 [Formula X wherein R1 is phenoxycarbonyl, R2=R3=R6=R7=R8=H, A is a saturated bond, R4 is hydroxyl and R5 is methoxy at the e position of the benzo ring] also cleaved DNA. Compound 41 was utilized at a 2 mM concentration at pH 5.0.
Compounds 40, 42 and 54 were further found to cause significant DNA cleavage when incubated at 5mM with supercoiled 0X174 DNA at pH 8.0 (Figure 2). Noteworthy in these studies is the observation of double strand cuts as well as single strand cuts, as is the case with dynemicin A (Compound 1). The methoxy derivatives 47, 55, 58 and 62 exhibited diminished activity against DNA.
On the other hand, the compounds exhibit anti10 microbial activity and all of those assayed exhibit some activity in vitro against tumor cells. A graph illustrating the inhibition of MIA PaCa-2 human pancreatic carcinoma cell growth using Compound 2 (DY-1) is shown in duplicate in Figure 3. Graphs illustrating the inhibition of MB-49 murine bladder carcinoma cell growth for Compounds 2 and 20 (DY-2) are shown in Figures 4 and 5, in quadruplicate and duplicate respectively. Values of IC50 obtained from the two wider range studies shown in Figure 4 were 43 nM and 91 nM. In a comparative study, Compound 2 was also shown to be more active against the cancerous MB-49 cells than against non-transformed CV-1 African green monkey kidney cells (ATCC CCL 70) or WI-38 human lung cells (ATCC CCL 75) .
Each of the dynemicin A analog Compounds 24a-g exhibited anti-tumor activity against MIA PaCa-2 cells, with the esters (Compounds 24b-g) being more potent than the free acid (Compound 24a). Compounds 24a-g were also active against MB-49 cells and inactive against CV-1 and WI-38 cells. Compounds 2b-d shown in below each exhibited weaker anti-tumor activity against MB-49 cells than did Compound 2.
The described chemistry supports the viability of two paths as triggering mechanisms for the dynemicin A-type cascade by showing that a lone pair of electrons on a heteroatom (N or 0) strategically positioned on the aromatic ring in relation to the epoxide moiety serves to initiate the cycloaromatization reaction. Such reactive species can be generated within the cell by enzymatic reactions, or as shown above, be released from suitable precursors under mild conditions in the laboratory. In addition, the relative stability and observation of Compounds 42, 54, 58 and 62 is interesting in that it allows for the scenario of bioreduction prior to intercalation as well as for the possibility of DNA interacting nucleophilically against quinone methide species. Thus the proposition that dynemicin A may be interacting with DNA by a dual mechanism (nucleophilic and radical) appears attractive, not only because of the observed preference for cleavage of adenine and guanine, but also in view of the chemistry of Compound 42.
Further biological evaluation data are provided hereinafter in Tables 1-3.
Best Mode for Carrying out the Invention Methods DNA Cleavage Studies The ethereal solution of Compound 40 produced by the LiAlH4 reduction of Compound 21 (39 mg, 0.10 mmol) was evaporated in vacuo to dryness and the residue dissolved in THF (4 mL) to give a 25 mM solution of Compound 40, assuming complete conversion of Compound 21. Analysis of Compound 40-induced damage to supercoiled, covalently closed, circular (form I) ΦΧ174 DNA was performed by incubation at varying concentrations of Compound 40 (100 μΜ - 5000 μΜ) in phosphate buffered aqueous solution at 37°C for 12-24 hours followed by agarose gel electrophoresis to separate the various DNA products.
Thus, a vial containing a 50 micromolar per base pair solution of φΧ174 Form I double stranded DNA in 2.0 microliters of pH 7.4 phosphate (50 mM) buffers were added 6.0 microliters of the same buffer solution and 2.0 microliters of a 5.0 millimolar ethanol solution of Compound 40.
The vials were then placed in a 37°C oven for 12-24 hours. A 2.0 microliter portion of glycerol loading buffer solution containing bromothymol blue indicator was added to each vial. A 10 microliter aliquot was then drawn from each. Gel electrophoresis analysis of the aliquots was performed using a 1.0 percent agarose gel with ethidium bromide run at 115 volts for 1 hour. DNA cleavage was indicated by the formation of nicked relaxed circular DNA (form II) or linearized DNA (form III), which was detected by visual inspection of the gel under 310 nanometer ultraviolet light using ethidium bromide.
Procedure for 6-Well Cytotoxicity Assay MIA PaCa-2 cells, MB-49, CV-1 or WI-38 cells were loaded into each well of a 6-well plate at a density of 100,000 cells/well in 3 ml culture medium.
They were incubated for 4 hours (37°C, 7 percent CO2).
Then 6 microliters of solution containing a compound to be assayed were added into 3 ml of medium (RPMI-1640, with 5 percent fetal bovine serum and 1 percent glutamine) in a 500X dilution so that in one well ethanol was added to make a 0.2 percent ethanol control. The plates were then incubated for 4 days (37°C, 7 percent C02). The medium was then drained, crystal violet dye (Hucker formula) was added to cover the well bottoms and then they were rinsed with tap water until rinses were clear. The stained cells were solubilized for quantitation with Sarkosyl solution (N-Lauryl sarcosine, 1 percent in water) at 3 ml/well. The absorbance of the solution was then read at 590-650 nm.
Large Scale Screening Against Cancerous Cell Lines In addition to the screening already discussed, several of the before-described compounds and chimeras were screened against several or all of a panel of ten cancerous cell lines as target cells. This screening utilized a sulforhodamine B cytotoxidity assay as discussed below.
SULFORHODAMINE B CYTOTOXICITY ASSAY 1. Preparation of target cells in 96-well plates a. Drain media from T^ flask of target cell line(s) and carefully wash cell monolayer two times with sterile PBS (approximately 5 mL per wash) b. Add 5 mL trypsin/EDTA solution and wash monolayer for approximately 15 seconds - 96 10 c. Drain all but approximately 1 mL of trypsin/EDTA from flask, cap flask tightly, and incubate at 37°C for approximately two to five minutes until cells come loose. d. Add 10-15 mL tissue culture (T.C.) medium (RPMI 1640 plus 10 percent fetal calf serum and 2 mM L-glutathione) to flask and pipet gently up and down to wash cells. e. Remove a 1/2 mL aliquot of the cell suspension and transfer to a glass 12 X 75 mm culture tube for counting. f. Count cells on a hemacytometer using trypan blue, and determine percent viability. g. Adjust volume of cell suspension with T.C. media to give a density of 1 X io5 cells/mL. h. Add 100 mL of T.C. medium to wells Al and BI of a 96-well plate for blanks. i. Add 100 mL of cell suspension to the remaining wells of the 96-well plates. j. Incubate plates for 24 hours at 37°C, -10 percent CO2 in a humidified incubator. 2. Preparation of sample drugs and toxic control a. Stock drug solutions were prepared by dissolving drug in the appropriate solvent (determined during chemical characterization studies) and sterile filtering the drug-solvent solution through a sterile 0.2 μ filter unit. An aliquot was taken from each filtered drug - 97 solution and the O.D. was measured to determine the drug concentration. b. Dilute the stock drug solution prepared above with T.C. medium to the desired initial concentration (1O'2-1O'4M) . A minimum volume of 220 mL of diluted drug is required per 96-well plate used in the assay. c. Prepare toxic control by diluting stock doxorubicin solution to 10‘7 to 10'9M in T.C. medium. A minimum volume of 300 pL is required per 96-well plate. 3. Addition of Sample Drugs, Compounds, Chimeras and 15 Controls to 96-well Plates a. Remove and discard 100 gL of T.C. medium from the wells in Column #2 of the 96well plate using a multi-channel pipettor and sterile tips. b. Add 100 mL of the initial compound dilution to adjacent duplicate wells in Columns #2. (Four materials can be tested in duplicate per 96-well plate.) c. Remove 10 pL of diluted compound from the wells in Column #2 and transfer to the corresponding wells in Column #3. Mix by pipetting up and down gently approximately five times. d. Transfer 10 pL to the appropriate wells in Column #4 and continue to make 1:10 dilutions of compound across the plate through Column #12. e. Remove and discard 100 pL of medium from wells FI, Gl, and Hl. Add 100 pL of toxic control (Doxorubicin diluted in T.C. medium) to each of these wells. f. Incubate (37°C, 5-10 percent CO2 in humidified incubator) plates for a total of 72 hours. Check plates at 24 hour intervals microscopically for signs of cytotoxicity. 4. Cell Fixation a. Adherent cell lines: 1. Fix cells by gently layering 25 /xL of cold (4°C) 50 percent trichloroacetic acid (TCA) on top of the growth medium in each well to produce a final TCA concentration of 10 percent. 2. Incubate plates at 4°C for one hour. b. Suspension cell lines: 1. Allow cells to settle out of solution. 2. Fix cells by gently layering 25 μΏ of cold (4°C) 80 percent TCA on top of the growth medium in each well. 3. Allow cultures to sit undisturbed for five minutes. 4. Place cultures in 4°C refrigerator for one hour. c. Wash all plates five times with tap water. d. Air dry plates.
Staining Cells a. Add 100 μΐ, of 0.4 percent (wt./vol.) Sulforhodamine B (SRB) dissolved in 1 . - 99 10 percent acetic acid to each well of 96well plates using multichannel pipettor. b. Incubate plates at room temperature for 30 minutes. c. After the 30 minute incubation, shake plates to remove SRB solution. d. Wash plates two times with tap water and 1 x with 1 percent acetic acid, shaking out the solution after each wash. Blot plates on clean dry absorbent towels after last wash. e. Air dry plates until no standing moisture is visible. f. Add 100 gL of lOmM unbuffered Tris base (ph 10.5) to each well of 96-well plates and incubate for five minutes on an orbital shaker. g. Read plates on a microtiter plate reader at 540 nM.
IC50 values; i.e the concentration of Compound required to kill one-half of the treated cells, were then calculated.
The cell lines assayed are listed below along with their respective sources: Cell Line NHDF Source and Type Normal human dermal fibroblasts, as controls - Clonetics Corporation Capan-1 American Type Culture Collection (ATCC) Molt-4 (All are human cancer cell lines as OVCAR-3 described by the ATCC) OVCAR-4 Sk-Mel-28 U-87 U-251 100 UCLA M-14 UCLA M-21 UCLA P-3 Dr. R. Reisfeld of The Scripps Research Institute, and originally obtained from Dr. D. Morton, University of California, Los Angeles. M-14 and M-21 are human melanoma cell lines, whereas P-3 is a human non-small cell lung carcinoma cell line.
Control studies were also carried out using the following well known anticancer drugs with the following IC50 values for NHDF and cancer cells.
Range of Average IC50 Values (Molarity) Drug NHDF Cancer Cells 15 Dexorubicin — 1.6X1O*10 - 9.8X10® Dynemicin A io-8 1.6X10 8 - 9.8X1O10* Calicheamicin 2.5X10'9 5X10’5 - 10*12** Morpholinodoxorubicin — 1.6X10'7 - 9.8X109 20 Taxol 10'8 10’7 - 10’9 Methotrexate 5X10*5 >10*4 - 10'® Cis-Platin 5X105 10’4 - IO’6 Melphelan 10’4 10’4 - IO'6 25 * UCLA-P3 cells were susceptible at 1O’12M. All other cells were susceptible at 1.56X10' M or higher concentrations.
** Molt-4 cells were susceptible at 1O'12M. All other 30 cells were susceptible at 3.9X10'9M or higher concentrations.
Tables 1 and 2 herein below provide average 35 IC50 data from five to all ten of the above cancer cells lines for fused ring enediyne compounds disclosed herein. Those tables provide a generic structure and a description of the R group of that generic structure for each compound. Compound numbers as provided hereinbefore are also provided. Table 3 contains data 101 for two fused-ring enediyne compounds (Compounds 47 and 120) as well as data for six chimers. 102 Table 1 Anticancer Activity (IC50) Of Enediyne Compounds Structure Number of Compound IC50(M)‘ 2: X = OH 6.3x10'® PhO^N*? •Ί 1 1 46: X = OMe 24b: X = OCH2CO2Me 6.3x1 O'5 5.0x1 O'6 24a: X = OCH2CO2H 6.3x10'® or * 21:X = H 5.0x10® ft 0 H J Λ 74: X = OH 2.0x10'®Ph0 ι V 76: X = H 7.9x10® & i xh>z PhO i X 85: X = OH 87: X χ H 2.0x10'® 3.2x10® R XHxk PhO^NLJSfPS 41:Χχ0Η 2.0x10® i X 41a: X χ H 2.0x10’® T MeOOJ 59a: X χ OH 7.9x1 O'7 (9.8x10®) T oq \ Ί 59b:X χ H 2.0x10'7 'BuCO/'C^ i (1.0x10'11)“ X * Average data obtained from 5-10 call lines. **Data obtained from MOLT-4 (Leukemia) cell line. 103 Table 2 Anticancer Activity (IC50) Of Enediyne Compounds Structure Number of Compound IC50 (M)‘ lHJj| 1,0 ΐ <Γ\Ί 21: R = Ph 21a: R = CH2CH2SPh 21b: R = CH2CH2SOPh 45: R = CH2CH2SO2Ph 5.0x10® 6.3x10® 3.2x10'® 2.0x10'7* ** ο h 76: R = Ph 77: R = CH2CH2SPh 70: R = CH2CH2SO2Ph 7.9x10® 3.6x10’® 3.2x10® 87: R = Ph 88: R = CH2CH2SPh 80: R = CH2CH2SO2Ph 3.2x10® 5.0x10® 1.6x10® IHJ 1 R0 KUL) φΤ MeO 41a: R = Ph 41b: R = CH2CH2SO2Ph 41c: R = CH2CH2SO2Ara 41d: R = CH2CH2SO2Arb 2.0x10'® 2.5x1 O'7** 2.0x1 O'7 1.3x1 O’7** Ar Ar„ = * Average data obtained from 5~10 cell fines.
**IC50 = 1.0x1 O'11 obtained from MOLT-4 (Leukemia) ceil line. - 104 Table 3 Anticancer Activity (IC5q) Of Enediyne Compounds IC5o (M) 120: X = OCH2CH2OH 125a: X = OCHsCt^ORi 126a: X = OCH2CH2OR2 125b: X = 0CH2CH20Ri 126b: X = OCH2CH2OR2 127a: X = OCH2CH2OR3 127b: X = OCH2CH2OR4 .0x10‘6 4.0x1 O'5 < 10*4 4.4x10*® < 10*4 8.7x10® 1.4x1 O'7** 7.6x10*® ou· FMOC OM· * Average data obtained from 5~10 cell lines.
**IC50 = 1.0x1 O'9 obtained from MOLT-4 (Leukemia) cell line. 105 As will be seen from the data of the tables, the compounds and chimeras had activities similar to those of the well known anticancer drugs.
Compounds having an R4 hydrogen tended to be 5 more active than those having an R4 hydroxyl or other oxygen-containing group. Compounds whose carbamate portion contained a phenylsulfonylethoxy or naphthylsulfonylethoxy group were about 10 to 100 times more active than similar compounds having a phenoxy group as part of the carbamate. Compounds having an electron releasing group relative to hydrogen para to the carbamate nitrogen atom tended to be equal to less active than those with hydrogen, whereas compounds with an intracellular-formed electron releasing group (e.g.
Compounds 59a and 59b) relative to hydrogen meta to that nitrogen atom tended to be more active than compounds having hydrogen at that position.
Turning to the chimeras, the data Table 3 indicate that the chimeras are effective. Those data also indicate that the presence of the FMOC group inhibits activity, but that presence of the oxime does not. Those data also indicate that chimeras having the stereochemistry of the calicheamicin oligosaccharide are more active than those having the epimeric stereochemistry at C-4 of the A ring.
The data of the tables also show compounds and chimeras described herein to be particularly active against Molt-4 leukemia cells. Thus, for those cells, Compounds 59b, 41b, 41c and 4Id exhibited IC50 values ,000 times more potent than the potency observed against the other cell lines. The activity of chimeric Compound 127a against Molt-4 cells was about 100-times that of the average of the other cell lines examined.
Those IC50 values against Molt-4 cells were also 10,000IE 912683 106 100,000 times smaller than the IC50 values for those compounds against NHDF cells.
Compound Preparation and Data Example 1: 7,8,9,10-Tetrahydrophenanthridine N-oxide (Compound 4a) A solution of 4 (1.42 g, 7.76 mmol) in dichloromethane (50 mL) was treated at 25°C with mCPBA (1.58 g of an 85 percent sample, 7.76 mmol) and stirred for 1 hour. The solution was poured into saturated sodium bicarbonate solution (50 mL) and extracted. The aqueous layer was extracted with further dichloromethane (2 x 50 mL), the combined organic layers were dried (Na2SO4), evaporated in vacuo, and the residue was purified by flash chromatography on silica eluting with 25 percent MeOH in EtOAc to give the pure N-oxide Compound 4a (1.24 g, 80 percent) as an off-white crystalline solid: Rf=0.34 (25 percent MeOH in EtOAc); mp 131.7°C (from EtOAc); IR (CDC13) 2950, 1580, 1390, 1300, 1210, 1140 cm'1; 1H NMR (500MHZ, CDC13) : S 8.72 (d, J=8.3 Hz, 1 Η, H-4), 8.31 (s, 1 Η, H-6), 7.91 (d, J=8.3 Hz, 1 Η, H-l), 7.68 (t, J=8.3 Hz, 1 Η, H-2 or H-3), 7.61 (t, J=8.3 HZ, 1 Η, H-2 or H-3), 3.02 (t, J=6.3 Hz, 2 H, H-10), 2.79 (t, J=6.3 Hz, 2 Η, H-7), 1.98-1.84 (m, 4 H); MS (FAB+) m/e (relative intensity) 200 (M+H, 100), 184 (12); HRMS calcd for C13H14NO (M+H) 200.1075, found 200.1055.
Example 2; Compound 2 A solution of enediyne 3 (205 mg, 0.50 mmol) in dry THF (10 mL) was cooled to -78°C and treated with lithium diisopropylamide (0.37 mL of a 1.5 M solution in cyclohexane, 0.56 mmol). After stirring 1 hour at -78°C, the reaction was quenched with saturated ammonium chloride solution (2 mL), allowed to warm to room 107 temperature, poured into saturated sodium bicarbonate solution (30 mL), and extracted with dichloromethane (3 x 50 mL). The combined organic extracts were dried (Na2SO4), evaporated in vacuo, and purified by flash chromatography on silica eluting with 50 percent ether in petroleum ether to give recovered 3 (48 mg, 23 percent), followed by the ten-membered enediyne Compound 2 (120 mg, 59 percent) as a white crystalline solid: Rf=0.42 (50 percent ether in petroleum ether); mp=22810 230°C dec. (from ether); IR (CDC13) νΜΧ 3420,2360,2330,1720 cm'1; ’h NMR (500 MHz, CDCl3) : 6 8.60 (dd, J=8.1, 1.3 Hz, 1 H, aromatic), 7.47-7.10 (series of multiplets, 8 H, aromatic), 5.83 (d, J=10.1 Hz, 1 H, olefinic), 5.67 (dd, J=10.1, 1.6 Hz, 1 H, olefinic), .53 (d, J=1.6 Hz, 1 H, C H-N), 2.35-1.71 (series of multiplets, 6 H, C H2) ; 13C NMR (125 MHz, CDC13) : δ 151.0, 135.8, 131.3, 129.3, 128.0, 127.8, 126.3, 125.8, 125.3, 124.0, 122.2, 121.6, 100.4, 94.3, 93.9, 88.8, 74.1, 73.2, 64.4, 50.5, 35.4, 23.2, 19.1; MS: m/e (relative intensity) 409 (26, M+), 368 (18), 236 (11), 162 (13), 131 (100); HRMS: calcd. for C26H19N04: 409.1314, found: 409.1314; Anal, calcd. for C26H19NO4.H20: C, 73.06; H, 4.95; N, 3.28. Found: C, 73.44; H, 5.04; N, 3.26.
Compounds 2-d were prepared from Compound 2 by reaction of Compound 2 with a mixture of the appropriate alcohol and its sodium salt as shown in Figure 15.
Example 3: N-Phenyloxycarbonyl-6-(3(Z)-hexene-1,5diynyl)-6a:10a-epoxy-10-oxo30 5,6,6a,7,8,9,10,10aoctahvdrophenanthridine (Compound 3) Silver nitrate (5.28 g, 31.2 mmol) was added to solution of the silyl acetylene Compound 13 (4.50 g, 9.36 mmol) in 100 mL of a H 20-EtOH-THF mixture (1:1:1) at 25°C, and the mixture was stirred until TLC analysis (30 percent ether in petroleum ether) indicated the consumption of 13 (approximately 1 hour). Potassium cyanide (4.32 g, 57.6 mmol) was then added and the mixture was stirred for 10 minutes. The mixture was poured into saturated sodium bicarbonate solution (100 mL) and extracted with dichloromethane (3 x 100 mL). The combined organic layers were dried (Na2SO4), evaporated in vacuo, and purified by flash chromatography on silica eluting with 30 percent ether in petroleum ether to give enediyne Compound 3 (2.30 g, 60 percent) as a colorless gum: Rf=0.38 (30 percent ether in petroleum ether); IR (CDC13) vMX 3304, 2940, 2240, 1720, 1492, 1378, 1321, 1206 cm'1; 1H NMR (500 MHz, CDClj): δ 8.87 (dd, J=7.8, 1.4 Hz, 1 Η, H-4), 7.53-7.09 (m, 8 H, aromatic), 5.93 (d, J=1.2 Nz, 1 Η, H-6), 5.78 and 5.79 (AB quartet, J=10.1 Hz, 2 H, olefinic), 3.16 (d, J=1.2 Hz, 1 H, CscH), 2.79-2.66 (m, 2 Η, H-9), 2.38-2.29 (m, 2 Η, H7), 2.04-1.89 (m, 2 Η, H-8) ; 13C NMR (125 MHz, CDClj): δ 150.9, 135.9, 130.0, 129.3, 128.8, 127.6, 125.9, 125.8, 123.0, 121.4, 120.4, 120.2, 90.6, 85.1, 82.8, 80.1, 75.1, 57.4, 48.1, 38.9, 23.9, 18.3; MS m/e (relative intensity) 409 (2, M+), 262(15), 212(18), 162(59), 58(100); HRMS: calcd. for C26H19N04: 409.1314, found: 409.1308.
Example 4: lO-Acetoxy-7,8,9,10tetrahvdrophenanthridine (Compound 5) A solution of 7,8,9,1030 tetrahydrophenanthridine N-oxide (Compound 4a) (1.23 g, 6.18 mmol) in acetic anhydride (50 mL) was heated to 100°C for 20 hours, evaporated to dryness, dissolved in dichloromethane (50 mL) and washed with saturated sodium bicarbonate solution (50 mL). The aqueous layer was extracted with dichloromethane (2 x 50 mL), the combined organic layers were dried (Na2SO4), evaporated in vacuo, 109 and the residue was purified by flash chromatography on silica eluting with Et2O to give pure Compound 5 (1.15 g, 77 percent) as a white crystalline solid: R f=0.33 (ether)? mp=128-129°C (from ether); IR (CDC13) vMX 2970, 1728, 1241 cm'1; 1H NMR (500 MHz, CDClj): S 8.70 (s, 1 H, H-6), 8.08 (d, J=9.5 Hz, 1 Η, H-4), 7.76 (d, J=9.5 Hz, 1 H, H-l), 7.63 (t, J=7.2 Hz, 1 Η, H-2 or H-3), 7.52 (t, J=7.2 Hz, 1 Η, H-2 or H-3), 6.57 (bs, 1 H, CH-OAc), 3.02 (bd, J=17.5 Hz, 1 Η, H-7), 2.88-2.80 (m, 1 Η, H-7), 2.27 (bd, J=13.8 Hz, 1 Η, H-9), 2.05 (s, 3 H, OAc), 2.01-1.88 (m, 3 H) ; 13C NMR (125 MHz, CDC13) : S 170.2, 152.3, 147.5, 137.8, 131.8, 130.1, 127.9, 127.0, 126.8, 122.2, 64.5, 29.1, 27.8, 21.7, 18.4; MS (FAB+) m/e (relative intensity) 242 (M+H, 100), 182 (23); HRMS calcd. for C15H16NO2 (M+H) 242.1181, found 242.1181; Anal, calcd. for C15H15NO2; C, 74.67; H, 6.27; N, 5.80. Found: C, 74.59; H, 6.31; N, 5.82.
Example 5: 10-Hydroxy-7,8,9,1020 tetrahvdrophenanthridine (Compound 6) A solution of Compound 5 (1.15 g, 4.77 mmol) in methanol (50 mL) was treated with potassium carbonate (200 mg, catalytic) and stirred for 1 hour. The solution was poured into saturated sodium bicarbonate solution (100 mL) and extracted with dichloromethane (1 x 100 mL, 2 x 50 mL). The combined organic layers were dried (MgSO4), evaporated in vacuo, and the residue was purified by flash chromatography on silica eluting with ethyl acetate to give alcohol Compound 6 (0.95 g, 100 percent) as a white crystalline solid: Rf=0.20 (ether); mp=176-177°C (from ether); IR (CDC13) νΜΧ 3600, 2950, 1510 cm'1; 1H NMR (500 MHz, CDClj): δ 8.51 (s, 1 H, H-6), 8.20 (d, J=9.1 HZ, 1 Η, H-4), 8.00 (d, J=9.1 Hz, 1 H, H-l), 7.61 (t, J=6.8 Hz, 1 H, H-2 or H-3), 7.55 (t, J=6.8 Hz, 1 H, H-2 or H-3), 5.39 (bs, 1 H, CH-OH), 2.89 110 (bd, J=16.1 Hz, 1 Η, H-7), 2.80-2.72 (m, 1 Η, H-7), 2.80-2.60 (bs, 1 H, OH), 2.24 (bd, J=12.5 Hz, 1 Η, H-8 or H-9), 2.07-1.88 (m, 3 H) ; MS (FAB+) m/e (relative intensity) 200 (M+H, 100), 154 (41), 136 (37), 109 (24)? HRMS calcd. for C,3H,4NO (M+H) 200.1075, found 200.1085.
Example 6: 10-tert-Butyldimethylsilyloxy-7,8,9,10tetrahvdrophenanthridine (Compound 7) A solution of Compound 6 (3.70 g, 18.6 mmol) in dry dichloromethane (100 mL) was treated with 2,6lutidine (3.4 mL, 27.9 mmol) and tert-butyldimethylsilyl triflate (5.35 mL, 22.3 mmol). After stirring for 1 hour at 25°C, methanol (2 mL) was added, stirring was continued for a further 5 minutes, and then the solution was poured into saturated sodium bicarbonate solution (100 mL) and extracted. The aqueous layer was extracted with further dichloromethane (2 x 50 mL), the combined organic layers were dried (Na2SO4), evaporated in vacuo and the residue was purified by flash chromatography on silica eluting with 50 percent ether in petroleum ether to give pure silyl ether Compound 7 (5.38g, 92 percent) as a white solid. 7: colorless oil; Rf=0.50 (70 percent ether in petroleum ether); IR (CDClj) νΜχ 2970, 2930, 2860 cm'1; 1H NMR (500 MHZ, CDClj) : S 8.68 (s, 1 Η, H-6) , 8.08 (d, J=4.7 Hz, 1 Η, H-l or H-4), 8.05 (d, J=4.7 Hz, 1 Η, H-l or H-4), 7.62 (t, J=4.7 HZ, 1 Η, H-2 or H-3), 7.53 (t, J=4.7 Hz, Η, H-2 or H-3), 5.45 (t, J=2.8 Hz, 1 Η, H-10), 3.00 (dd, J=5.5, 16.6 Hz, 1 H, CH-Ar), 2.81 (m, 1 H, CH-Ar), 2.23-2.10 (m, 2 H, CH2) , 1.88-1.78 (m, 2 H, CH2) , 0.84 (s, 9 H, rBu) , 0.22 (S, 6 H, SiMe2) ; 13C NMR (125 MHz, CDClj); 6 152.8, 147.0, 141.2, 129.8, 129.3, 127.9, 126.9, 126.1, 123.6, 63.2, 31.8, 27.0, 25.8, 18.2, 16.4, -3.6, -4.5; MS (FAB+) m/e (relative intensity) 314 (M+H, - Ill 100), 256 (7), 182 (11)? HRMS calcd. for C19H28NOSi (M+H) 314.1940, found 314.1951.
Example 7: N-Phenyloxycarbonyl-10-tert5 butyldimethylsilyloxy-6-ethyl5,6,7,8,9,10-hexahydrophenanthridine (Compound 8) A solution of quinoline Compound 7 (5.20 g, 16.6 mmol) in dry THF (166 mL) was cooled to -78°C and treated with ethynylmagnesium bromide (36.5 mL of a 0.5 M solution in THF, 18.3 mmol) followed by phenyl chloroformate (2.3 mL, 18.3 mmol). The solution was allowed to warm up slowly to 25°C over 1 hour, quenched with saturated ammonium chloride solution (10 mL), poured into saturated sodium bicarbonate solution (150 mL) and extracted. The aqueous layer was extracted with dichloromethane (2 x 100 mL), the combined organic layers were dried (Na2S04), evaporated in vacuo, and purified by flash chromatography on silica eluting with 10 percent ether in petroleum ether to give pure carbamate Compound 8 (6.96 g, 92 percent) as a colorless oil (about 3:1 mixture of isomers as judged by NMR). Rf=0.85 (30 percent ether in petroleum ether); IR (CDC13) Ymax 3300, 2952, 2858, 2250, 1715, 1473, 1204 cm'1; 1H NMR (500 MHz, CDC13) : S 7.68 (d, J=7.5 Hz, 1 H, H-4), 7.40-7.12 (m, 8 H), 5.68, 5.61 (2 X s, 1 Η, H-6), 5.00, 4.69 (2 x bs, 1 H, H-10), 2.50-1.50 (m, 7 H), 0.80, 0.92 (2 X s, 9 H, lBu), 0.28, 0.19, 0.10, 0.09 (singlets, 6 H, SiMe2) ; 13C NMR (125 MHz, CDC13) ; S 151.1, 136.3, 132.9, 129.8, 129.3, 127.2, 126.0, 125.4, 125.1, 124.2, 124.1, 123.9, 122.0, 80.2, 72.3, 65.0 and 64.2, 48.7 and 48.2, 32.3 and 31.4, 28.0, 26.1, 18.4 and 16.3, -4.1 and -4.8; MS m/e (relative intensity) 459 (M*, 10), 402 (100), 366 (10), 308 (24), 206 (26), 151 112 (27) , 75 (29); HRMS calcd. for C28H33O3NSi (M*) : 459.2230, found: 459.2233.
Example 8: N-Phenyloxycarbonyl-10-tert5 butyldimethylsilyloxy-6a:1 Oa-epoxy6-ethyl-5,6,6a,7,8,9,10,10aoctahvdrophenanthridine ί Compound 9) A solution of Compound 8 (8.60 g, 18.8 mmol) in dichloromethane (120 mL) was treated with mCPBA (8.08 g of a 60 percent sample, 37.6 mmol) and stirred at 25°C for 3 hours. The solution was poured into saturated sodium bicarbonate solution (lOOmL), extracted, and the aqueous layer extracted with further dichloromethane (2 x 100 mL). The combined organic layers were dried (Na2S04) , evaporated in vacuo, and the residue was purified by flash chromatography on silica eluting with 10 percent ether in petroleum ether to give epoxide Compound 9 (8.20 g, 92 percent) as a white foam (mixture of two isomers, about 3:1 ratio); Rf=0.73 (30 percent ether in petroleum ether); IR vMX (CDC13) 3307, 2953, 2250, 1721, 1494, 1384, 1322, 1250, 1207 cm'1; 1H NMR (500 MHz, CDClj): «5 7.88 (d, J=7.1 Hz, 1 H, H-4), 7.507.10 (m, 8 H), 5.58 (bs, 1 Η, H-6), 4.82 (dd, J=10.0, .7 HZ, 1 Η, H-10), 2.34 (dd, J=14.8, 5.6 Hz, 1 H), 2.09 (bs, 1 H), 1.95-1.85 (m, 2 H), 1.78-1.62 (m, 2 H), 1.401.30 (m, 1 H) ; 13C NMR (125 MHz, CDClj): δ 153.9 and 151.1, 135.5, 129.2, 129.2, 129.1, 128.3, 128.1, 127.9, 127.1, 125.5, 121.6, 78.5, 73.8, 72.8, 69.9, 60.4, 48.0, 31.0 and 29.6, 26.0 and 25.8, 24.0, and 26.5, 18.2 and .3, -0.28, -0.28, -0.37; MS: m/e (relative intensity) 475(M*,2), 419 (100), 325 (28), 268 (10), 222 (14), 151 (18), 73 (42); HRMS: calcd. for C28H33O4NSi (M*): 475.2179, found: 475.2175. 113 Example 9: N-Phenyloxycarbonyl-6a:10a-epoxy-6-ethyl10-hydroxy-5,6,6a,7,8,9,10,10aoctahvdrophenanthridine (Compound 10) A solution of epoxide Compound 9 (8.20 g, 17.4 mmol) in THF (lOOmL) was treated with TBAF (20.9 mL of a 1 M solution in THF, 20.9 mmol) and heated to 42°C for three hours. The solution was evaporated in vacuo and purified by flash chromatography on silica eluting with 50 percent Et2O/petroleum ether to give pure alcohol Compound 10 (6.00 g, 100 percent) as a white crystalline solid (about 3:1 mixture of isomers as shown by NMR). Rf=0.31 (50 percent ether in petroleum ether); mp 78-79°C (from Et20) ; IR (CDC13) νΜχ 3580, 3306, 2951, 2250, 1720, 1595, 1494, 1382, 1322, 1206 cm*1; 1H NMR (500 MHZ, CDC13) : δ 7.91 and 7.88 (d, J=8.0 Hz, 1 H, H-4), 7.50-7.08 (m, 8 H), 5.62 and 5.59 (d, J=1.0 Hz, 1 Η, H-6), 4.89 and 4.70 (m, 1 Η, H-10), 2.47-1.35 (m, 8 H) ; 13C NMR (125 MNz, CDC13) : i 150.9, 135.5, 129.3, 128.7, 128.6, 128.4, 127.7, 127.3, 126.1, 125.8, 121.5, 78.7 and 78.2, 74.8 and 70.8, 73.2, 66.6, 65.9 and 64.4, 60.9 and 58.2, 47.8, 30.3 and 27.0, 24.1 and 19.0, 15.2 and 13.8; MS m/e (relative intensity) 361 (M*,65), 224 (100), 196 (24), 180 (29), 167 (30), 94 (40), 77 (45); HRMS: calcd. for C22H19N04 (M+) ; 361.1314, found: 361.1317.
Example 10: N-Phenyloxycarbonyl-6a:10a-epoxy-6-ethyl10-OXO-5,6,6a,7,8,9,10,10aoctahvdrophenanthridine (Compound 11) Alcohol Compound 10 (6.009, 17.4 mmol) was dissolved in dry dichloromethane (180 mL) and treated with powdered, activated 4A molecular sieves (1 g) and pyridinium chlorochromate (6.25 g, 29.0 mmol). The suspension was stirred for 1 hour at 25°C, filtered through celite, concentrated in vacuo, and the residue 114 was purified by flash chromatography on silica eluting with 30 percent Et20/petroleum ether to give ketone Compound 11 (4.49 9,75 percent) as a white foam: Rf=0.51 (50 percent ether in petroleum ether) ; IR (CDC13) vmax 3306, 2259, 1721, 1491, 1321, 1206 cm'1; 1H NMR (500 MHz, CDClj): δ 8.50 (d, J=7.8 Hz, 1 Η, H-4), 7.53-7.10 (m, 8 H, aromatic), 5.73 (d, J=2.4 Hz, 1 Η, H-6), 2.76 (dt, J=15.2, 4.9 Hz, 1 Η, H-9), 2.60 (ddd, J=15.2, 10.4, 6.1 HZ, 1 H, H-9), 2.37-2.28 (m, 2 Η, H-7), 2.21 (bs, 1 H, C=C-H), 2.04-1.90 (m, 2 Η, H-8); 13C NMR: (125 MHz, CDC13): δ 201.0, 153.9, 151.0, 135.8, 129.9, 129.3, 129.0, 127.6, 126.1, 125.9, 123.0, 121.5, 77.7, 74.9, 74.2, 57.4, 47.3, 38.9,23.8, 18.3; MS m/e (relative intensity) 359 (M+, 100), 266 (52), 222 (65), 194 (54), 180 (51) , 146 (45) , 69 (80) ; HRMS calcd. for C22H17N04 (M+): 359.1158, found: 359.1154; Anal, calcd. for C22H17NO4: C, 73.53; H, 4.77; N, 3.90. Found: C, 73.27; H, 4.79; N, 3.91.
Example 11: N-Phenyloxycarbonyl-6-[6-trimethylsilyl3(Z)-hexene-1,5-diynyl]-6a:10aepoxy-10-oxo-5,6,6a,7,8,9,10,10aoctahvdrophenanthridine (Compound 13) Palladium11 acetate (192 mg, 0.86 mmol) and triphenylphosphine (832 mg, 3.17 mmol) in dry, degassed benzene (10 mL) were heated under argon at 60°C for 1 hour. The resulting dark red solution was cooled to 25°C, and the (Z)-chloroenyne Compound 12 (2.88 g, 18.2 mmol) in dry, degassed benzene (20 mL) was added, followed by n-butylamine (1.92 mL, 19.4 mmol). The solution was stirred for 15 minutes at 25°C, cooled to zero degree C, and the acetylene 11 (4.49g, 12.5 mmol) in dry, degassed benzene (50 mL) was added, followed by copper (I) iodide (512 mg, 2.69 mmol). The solution was stirred for 2 hours at 25°C, poured into saturated - 115 sodium bicarbonate solution (100 mL) and extracted. The aqueous layer was extracted with dichloromethane (2 x 50 mL), the combined organic layers were dried (Na2S04) , evaporated in vacuo, and the residue was purified by flash chromatography on silica eluting with 20 percent ether in petroleum ether to give the coupled product Compound 13 (4.50 g, 74 percent) as a colorless gum: Rf=0.51 (30 percent ether in petroleum ether); IR (CDC13) VMX 2962, 1720, 1492, 1378, 1322, 1252, 1206, 846 cm1; 1H NMR (500 MHz, CDClj): S 8.36 (d, J=8.5 Hz, 1 Η, H-4), 7.52-7.09 (m, 8 H, aromatic), 5.99 (d, J=1.6 Hz, 1 Η, H-6), 5.82 (d, J=11.2 Hz, 1 H, olefinic), 5.66 (dd, J=11.2, 1.6 Hz, 1 H, olefinic), 2.76 (dt, J=15.3, 4.7 Hz, 1 Η, H-9), 2.71 (ddd, J=15.3, 10.8, 6.1 Hz, 1 H, H-9), 2.39-2.30 (m, 2 Η, H-7), 2.07-1.89 (m, 2 Η, H-8), 0.25 (s, 9 H, SiMe3) ; 13C NMR (125 MHz, CDClj): S 201.1, 150.9, 135.8, 129.9, 129.2, 128.9, 128.4, 127.7, 126.0, 125.8, 122.9, 121.4, 120.8, 118.9, 103.6, 101.5, 90.4, 83.0, 74.9, 57.5, 48.3, 38.9, 23.9, 18.2, 0.00; MS m/e (relative intensity) 481 (M*,ll), 360 (100), 146 (10); HRMS: calcd. for C29H2704NSi (M+) : 481.1709, found: 481.1705.
Example 12: Compound 2¾ A solution of enediyne Compound 2 (100.1 mg, 0.224 mmol) in pyridine (2 mL) was treated with acetic anhydride (0.50 mL, 5.31 mmol) and DMAP (10 mg, catalytic) at 25°C. After 2 hours, the reaction mixture was poured into saturated sodium bicarbonate solution (25 mL), extracted with dichloromethane (3 x 25 mL), the combined organic layers were dried (Na2SO4) , evaporated in vacuo, and the residue was purified by flash chromatography (silica, 30 percent ether in petroleum ether) to give acetate Compound 2a (110.7 mg, 100 percent). 2a: white crystalline solid, mp 212-214°C - 116 dec. (from ether); Rf=0.55 (50 percent ether in petroleum ether)? IR (CDC13) 3075, 2950, 2215, 1742, 1720, 1500, 1216, 769 cm*1? 1H NMR (500 MHz, CDClj) : δ 7.92 (d, J=8.1 Hz, 1 H, aromatic), 7.50-7.09 (m, 8 H, aromatic), 5.83 (d, J=10.1 Hz, 1 H, olefinic), 5.65 (d, J=10.1 Hz, 1 H, olefinic), 5.53 (s, 1 H, N-CH(C)-C), 2.51-1.70 (m, 6 H, CH2) , 2.18 (s, 3 H, OAc) ? 13C NMR (125 MHZ, CDC13): δ 169.1, 150.8, 130.0, 129.3, 128.4, 128.1, 128.0, 127.2, 126.8, 125.7, 125.2, 124.3, 122.9, 121.5, 97.9, 96.5, 93.7, 88.9, 78.0, 73.5, 62.6, 50.3, 29.8, 22.7, 21.8, 18.8? MS (FAB+) m/e (relative intensity) 452 (M+H, 52), 410 (37), 392 (100), 316 (32), 272 (43), 242 (30), 154 (77), 136 (70); HRMS calcd. for C28H28NO5 (M+H) 452.1498, found 452.1469.
A solution of enediyne Compound 2a (93.0 mg, 0.206 mmol) and 1,4-cyclohexadiene (1.0 mL) in benzene (3.0 mL) was treated with p-toluene-sulfonic acid (39 mg, 0.23 mmol) and stirred at 60°C for 2 hours. The solvent was removed in vacuo and the residue purified by flash chromatography (silica, 50 percent ether in petroleum ether) to give diol acetate Compound 15a (80.2 mg, 83 percent). 15a: while crystalline solid, mp 198200°C (from ether).
Example 13: Compound 15 Colorless solid: R#=0.22 (50 percent ether in petroleum ether)? IR (CDC13) 3360, 3072, 2950, 1738, 1715, 1500, 1192 cm'1? 1H NMR (500 MHz, CDC13) : δ 7.57 (d, J=7.8 Hz, 1 H, aromatic), 7.40-7.01 (series of multiplets, 12 H, aromatic), 6.83 (bs, 1 H, OH), 5.59 (s, 1 H, N-C H(C)-C), 3.17 (m, 1 H, CH2) , 2.28 (m, 1 H, CH2), 2.26 (s, 3 H, OAc), 1.80-1.40 (series of multiplets, 3 H, CH2)·, 0.72 (m, 1 H, CH2) ; 13C NMR (125 MHz, CDClj): 5 174.9, 150.8, 137.7, 134.8, 133.5, 129.7, 129.3, 129.2, 129.0, 128.8, 128.5, 128.2, 127.8, 127.7, - 117 ~ 125.5, 124.8, 123.4, 121.8, 93.8, 75.1, 70.6, 61.4, 32.5, 31.4, 22.6, 19.8; MS; m/e (relative intensity) 471 (M+, 19), 245 (100), 162 (100), 94 (42); HRMS: calcd. for C28H2506N (M*): 471.1682, found: 471.1683; Anal. calcd. for C28H25O6N: C, 71.33; H, 5.34; N, 2.97. Found: C, 71.36; H, 5.54; N, 2.84.
Example 14: Compound 15b Dry HCl gas was bubbled through a solution of 10 acetate Compound 2a (32 mg, 0.071 mmol) and 1,4cyclohexadiene (40 mg, 0.32 mmol) in dichloromethane (4 mL) at 25°C for 30 seconds. The solvent was removed in vacuo and the residue purified by flash chromatography (silica, 50 percent ether in petroleum ether) to give the chloride, Compound 15b (25 mg, 80 percent).
Colorless gum; Rf=0.21 (50 percent ether in petroleum ether); IR (CDC13) 3500, 2945, 1710, 1492, 1400, 1225, 789 cm'1; ’h NMR (500 MHz, CDC13) : S 7.72 (d, J=8.1 Hz, 1 H, aromatic), 7.45-6.96 (m, 12 H, aromatic), .85 (s, 1 H, benzylic), 2.56 (bs, 1 H, OH), 2.37 (bs, 1 H, OH), 2.34-1.42 (m, 6 H, CH2) ; 13C NMR (125 MHZ, CDClj) : 5 151.2, 134.7, 132.6, 130.4, 129.4, 129.3, 128.6, 128.5, 128.2, 128.2, 128.1, 127.5, 125.7, 124.5, 124.2, 124.0, 121.7, 81.2, 80.4, 70.2, 62.7, 35.4, 33.7, 18.8; MS (FAB+): m/e (relative intensity) 580 (M+Cs, 100), 419 (42), 286 (100), 154 (37); HRMS: Calcd. for C26H22°4NC1Cs (M+Cs) : 580.0291, found: 580.0286.
Example 15: Compound 17 Compound 17 has been prepared by several methods as indicated below.
Method (i): A solution of the cobalt complex Compound 19 (42 mg, 0.060 mmol) in CH2C12 (1 mL) was treated with Et3N*-O' (32.7 mg, 0.29 mmol) and stirred at °C for 4 hours. The solution was poured into - 118 saturated sodium bicarbonate solution (25 mL) and extracted with CH2C12 (3 x 25 mL). The combined organic layers were dried (MgSO4), evaporated in vacuo and purified by flash chromatography to give the aromatized product Compound 17 (17.7 mg, 83 percent).
Method (ii): A solution of enediyne Compound 2 (57.8 mg, 0.141 mmol) and 1,4-cyclohexadiene (0.5 mL) in benzene (1.5 mL) was treated with p-toluenesulfonic acid (29.6 mg, 0.155 mmol) and stirred at 25°C for 24 hours.
The solvent was removed in vacuo and the residue purified by flash chromatograph (silica, 50 percent ether in petroleum ether) to give keton Compound 17 (53.7 mg, 92 percent).
Method (iii) : Trimethylsilyl triflate (15 μ1>, 0.08 mmol) was added to a solution of enediyne Compound (32 mg, 0.078 mmol) and triethylsilane (40 mg, 0.32 mmol) in dichloromethane (2 mL) at -78°C. After five minutes, the mixture was quenched at -78°C with saturated ammonium chloride solution (1 mL), diluted with either (10 mL), washed with water (2x3 mL), brine (3 mL) and dried (MgSO4) . The organic solvent was removed in vacuo and the residue was purified by flash chromatograph (silica, 50 percent ether in petroleum ether) to give ketone Compound 17 (22 mg, 68 percent).
Method (iv); Dry HC1 gas was bubbled through a solution of enediyne Compound 2 (32 mg, 0.078 mmol) and 1,4-cyclohexadiene (40 mg, 0.32 mmol) in dichloromethane (4 mL) at 25°C for 30 seconds. The solvent was removed in vacuo and the residue purified by flash chromatography (silica, 50 percent ether in petroleum ether) to give Compound 17 (25 mg, 78 percent).
White crystals; Rf=0.63 (70 percent ether in petroleum ether); mp=191-193°C (from methylene chloride/ether) ; IR (CDC13) 3480, 3080, 2935, 1712, 1490, 1264, 1192 cm'1; 1H NMR (500 MHz, CDC13) : δ 8.33 - 119 (dd, J=7.9, 1.3 Hz, 1 H, aromatic), 8.09 (d, J=7.5 Hz, 1 H, aromatic), 7.54-7.02 (m, 11 H, aromatic), 5.65 (s, 1 H, benzylic), 2.75 (bs, 1 H, OH), 2.69-1.80 (m, 6 H, CH2) ; 13C NMR (125 MHz, CDClj): 6 207.5, 153.0, 150.9, 148.2, 137.1, 134.2, 129.8, 129.5, 128.5, 128.2, 127.8, 127.1, 126.1, 126.0, 124.3, 122.8, 121.8, 121.3, 82.5, 65.0, 64.1,40.0, 30.2, 23.5; MS; m/e (relative intensity) 411 (M*,100), 318 (58), 274 (49), 246 (12), 217 (55), 94 (29); HRMS; Calcd. for C26H21O4N (M+) : 411.1471, found: 411.1468; Anal. Calcd. for C26H21O4N: C, 75.90; H, 5.14; N, 3.40. Found: C, 75.66; H, 5.45; N, 3.14.
Example 16: Compound 18 A solution of the enediyne Compound 2 (124 mg, 0.30 mmol) in CH2C12 (4 mL) was treated with Co2(CO)8 (260 mg, 0.76 mmol) and stirred at 25°C for 5 minutes. The solution was concentrated in vacuo and the residue was purified by flash chromatography to give the cobalt complex Compound 18 (291 mg, 98 percent).
Green crystalline solid; mp>300°C (from ether); Rf=0.80 (50 percent ether in petroleum ether); IR (CDClj) 3500, 2950, 2872, 2095, 2070, 2025, 1725, 1492, 1207 cm'1; 1H NMR (500 MHz, CDClj): S 8.87 (bs, 1 H, aromatic), 7.61-7.02 (m, 8 H, aromatic), 6.47 [bs, 1 H, N-CH(C)-C], 6.38 (bd, J=10.7 Hz, 1 H, olefinic), 6.19 (bd, J=10.7 HZ, 1 H, olefinic), 3.50 (bs, 1 H, OH), 2.70-1.71 (m, 6 H,CH2) ; 13C NMR (125 MHz, CDClj) : δ 199.1, 198.6, 197.8, 151.3, 134.9, 132.9, 130.9, 129.4, 128.8, 127.2, 125.8, 125.3, 125.1, 124.8, 123.4, 121.6, 98.5, 88.9, 81.5, 80.1, 78.0, 73.9, 63.1, 59.0, 44.2, 24.9, 17.1; MS (FAB+) m/e (relative intensity) 1114 (M+CS, 11), 1086 (M+Cs-CO, 18), 1058 (M+CS-2CO, 6), 1030 (M+CS-3CO, 19), 1002 (M+CS-4CO, 11), 943 (M+CS-4CO-CO, ), 918 (11), 890 (24), 862 (34), 813 (100); HRMS 120 calcd. for C38H19016NCo4Cs (M+Cs) 1113.7086, found 1113.7001.
Example 17: Compound 19 A solution of the cobalt complex Compound 18 (291 mg, 0.30 mmol) in CH2C12 (4 mL) was treated at zero degree C with trifluoroacetic acid (68.6 ph, 0.89 mmol), After 5 minutes, the mixture was poured into saturated sodium bicarbonates solution (25 mL) and extracted with CH2C12 (3 x 25 mL) . The combined organic layers were dried (MgSO4), evaporated in vacuo, and purified by flash chromatography (silica, 50 percent ether in petroleum ether) to give the ketone Compound 19 (167.4 mg, 81 percent).
Brown crystalline solid; mp >300°C (from ether); Rf=0.25 (50 percent ether in petroleum ether); IR (CDC13) 3408, 2945, 2100, 2065, 2032, 1875, 1735, 1680, 1512, 1217 cm'1; 1H NMR (500 MHz, CDClj); δ 7.81 (d, J=8.2 Hz, 1 H, aromatic), 7.42-7.11 (m, 8 H, aromatic), 7.00 (d, J=10.2 Hz, 1 H, olefinic), 6.39 [s, H, N-C H(C)-C], 5.52 (d, J=10.2 Hz, 1 H, olefinic), 3.35-1.82 (m, 7 H, CH2, OH); 13C NMR (125 MHz, CDClj): δ 202.9, 198.9, 198.1, 154.3, 150.9, 144.0, 133.2, 132.8, 129.6, 128.3, 128.1, 126.7, 126.0, 125.8, 123.3, 121.8, 108.7, 93.2, 92.5, 82.1, 81.0, 68.5, 56.2, 38.0, 30.2, 21.6; MS (FAB+) m/e (relative intensity) 828 (M+Cs, 17), 800 (18), 688 (74), 639 (20), 555 (32), 527 (100); HRMS calcd. for c32H19NO10co2Cs (M+Cs) 827.8727, found 827.8730; Anal, calcd. for C32H19NO10Co2: C, 55.27; H, 2.75; N, 2.01; Co, 16.97. Found: C, 54.98; H, 2.79; N, 1.86; Co, 15.22.
Example 18: Compound 20 Thiocarbonyldiimidazole (180 mg, 0.99 mmol) was added to a solution of the alcohol Compound 2 (137 mg, 121 0.335 mmol) and 4-dimethylaminopyridine (DMAP) (25 mg, 0.18 mmol) in dichloromethane (2 mL) at 25°C. After 48 hours, the solution was concentrated in vacuo and the residue purified by flash chromatography (silica, 80 percent ether in petroleum ether) to give thionoiroidazolide 20 (160 mg, 95 percent). 20: white crystalline solid, mp 178-179°C dec. (from ether/dichloromethane); Rf=0.62 (70 percent ether in petroleum ether); IR (CDClj) 3042, 2912, 2195, 1710, 1500, 1495, 1212, 1105 cm'1; 1H NMR (500 MHz, CDC13) : 5 8.49 (s, 1 H, N-CH=N), 7.71-7.05 (m, 11 H, aromatic), 5.93 (d, J=10.3 Hz, 1 H, olefinic), 5.73 (dd, J=10.3, 1.6 Hz, 1 H, olefinic), 5.60 (d, J=1.6 Hz, 1 H, N-CHCsC), 3.08 (d, J-ll.l Hz, 1 H, CH2) , 2.46-1.70 (m, 5 H, CH2) ; 13C NMR (125 MHz, CDClj) : S 179.1, 153.4, 151.0, 137.0, 135.9, 130.9, 129.4, 129.3, 128.2, 127.0, 126.4, 125.8, 125.4, 123.9, 123.2, 121.3, 117.7, 100.6, 94.3, 93.9, 88.9, 85.4, 74.5, 65.9, 63.2, 50.3, 28.0, 22.7, 18.4; MS (FAB+) m/e (relative intensity) 653 (M+Cs, 21), 419 (19), 379 (15), 286 (100), 154 (30); HRMS Calcd. for C30H21N3°4SCs (M+Cs) 653.0385, found 653.0360; Anal, calcd. for C30H21N3O4S: C, 69.35; H, 4.07; N, 8.09; S, 6.17. Found: C, 69.01; H, 4.17; N, 7.91; S, 6.19.
Example 19: Compound 21 A solution of the imidazolide Compound 20 (112 mg, 0.24 mmol), azobisisobutyronitrile (AIBN; 3 mg) and tri-n-butylstannane (n-Bu3SnH) (94 gL, 0.36 mmol) was heated at 75°C for 2 hours, the solvent was removed in vacuo, and the residue was purified by flash chromatography to give the deoxygenated product Compound (71 mg, 75 percent).
White crystals; Rf=0.62 (30 percent ether in petroleum ether); mp 248-250°C dec. (from ether); IR(CDC13) νΜχ 2945, 2872, 2232, 2205, 1712, 1465, 1325, 122 1185 cm'1; 1H NMR (500 MHz, CDClj): δ 7.67 (d, J=7.5 Hz, H, aromatic), 7.6-7.14 (m, 8 H, aromatic), 5.84 (dd, J=10.5, 1.6 Hz, 1 H, olefinic), 5.72 (dd, J=10.5, 1.6 Hz, 1 H, olefinic), 5.57 (d, J=1.6 Hz, 1 H, N-CH-Cs), 3.85 (d, J=1.6 Hz, 1 H, C®C-CH-C), 2.49 (m, 1 H, CH2) , 2.30 (m, 1 H, CH2) , 2.12-1.60 (m, 4 H, C H2) ; 13C NMR (125 MHz, CDClj): δ 151.0, 135.5, 129.4, 129.4, 128.2, 127.3, 125.8, 125.8, 125.4, 125.0, 122.0, 122.0, 121.5, 101.8, 94.9, 91.4, 88.8, 70.5, 61.1, 50.0, 29.8, 22.9, 22.5, 15.5; MS: m/e (relative intensity) 393 (20,M*) , 294(9), 262(15), 212 (11), 149 (42); HRMS: Calcd. for C26H19°jN (M*) : 393.1365, found: 393.1332.
Example 20: Compound 23 A solution of the enediyne Compound 21 (30 mg, 0.076 mmol) and 1,4-cyclohexadiene (0.5 mL) in benzene (2 mL) was treated with TsOH.H2O (18 mg, 0.09 mmol) and stirred at 25°C for 24 hours. The solvent was removed in vacuo and the residue was purified by flash chromatography to give the diol Compound 23 (26 mg, 85 percent).
Colorless gum; Rf=0.35 (50 percent ether in petroleum ether); IR (CDClj) 3310, 3082, 2925, 1705, 1592, 1395, 1200 cm'1; ’h NMR (500 MHz, CDClj): δ 7.58 (bd, J=4.4 Hz, 1 H, aromatic), 7.47 (bd, J=7.8 Hz, 1 H, aromatic), 7.40-7.09 (m, 10 H, aromatic), 6.81 (d, J=8.1 Hz, 1 H, aromatic), 5.78 (s, 1 H, N-benzylic), 4.00 (bs, H, OH), 3.24 (s, 1 H, benzylic), 2.42-0.72 (m, 6 H, CH2) ; 13C NMR (125 MHz, CDC13) : 6 151.0, 138.2, 134.7, 129.4, 129.4, 129.3, 128.8, 128.4, 128.3, 127.1, 126.9, 125.7, 125.0, 124.4, 121,8, 121.8, 121.5, 83.0, 66.2, 65.1, 51.2, 33.5, 27.1, 18.7; MS(FAB+): m/e (relative intensity) 546 (15, M+Cs), 379 (31), 312 (30), 286 (100); HRMS: Calcd. for C26H23O4NCs (M+Cs) : 546.0681, found: 546.0691. 123 Example 21: Compound 23a HCI gas was bubbled through a solution of the enediyne Compound 21 (30 mg, 0.076 mmol) and 1,4cyclohexadiene (0.5 mL) in CH2C12 at 25°C for 30 seconds The solvent was removed in vacuo and the residue was purified by flash chromatography to give the chloride Compound 23a (27 mg, 84 percent).
Pale yellow solid; mp=114-116°C; Rf=0.62 (50 percent ether in petroleum ether); IR (CDC13) 3500, 3065, 2932, 1712, 1495, 1382, 1200 cm'1; 1H NMR (500 MHz CDC13) : 5 7.71-6.73 (m, 13 H, aromatic), 5.87 (s, 1 H, N-benzylic), 3.62 (s, 1 H, benzylic), 2.52 (bs, 1 H, OH), 2.50-1.60 (m, 6 H, CH2) ; MS: m/e (relative intensity) 564 (5, M+Cs), 419 (100), 379 (58); HRMS: Calcd. for C26H22O3NC1Cs (M+Cs): 564.0343, found: 564.0351.
Example 22: Compound 24c Ethyl bromoacetate (27 mg, 0.16 mmol) was added to a mixture of the alcohol Compound 2 (34 mg, 0.08 mmol) and Cs2CO3 (67 mg, 0.2 mmol) in anhydrous DMF (2 mL) at 60°C. The mixture was heated for 3 hours, diluted with ether (10 mL), washed with NH4C1 (2x3 mL), water (2x2 mL), and brine (2 mL). The organic layer was dried (MgSOJ and purified by flash chromatography to give the ester Compound 24c (37.5 mg, 91 percent.
Colorless oil; Rf=0.55 (50 percent ether in petroleum ether); ’h NMR (500 MHz, CDC13) : δ 8.63 (d, J=10.3 Hz, 1 H aromatic), 7.45-7.10 (m, 8 H, aromatic), .82 (d, J=10.5 Hz, 1 H, olefinic), 5.68 (dd, J=10.5, 1.5 Hz), 1 H, olefinic), 5.51 [d, J=1.5 Hz, 1 H, CsC(C)CHN], 4.34 [d, J=15.6 Hz, 1 H, C(O)CH2O], 4.28 [d=15.6 HZ, 1 H, C(O)CH2O], 4.24 (m, 2 H, OCH2CH3) , 2.3535 1.70 (m, 6 H, CH2), 1.30 (5, J=8.2 Hz, 3 H, OCH2CH3) ; 13C 124 NMR (125 MHz, CDClj): 5 169.5, 150.9, 135.6, 131.0, 129.3, 129.3, 128.1, 127.7, 125.7, 125.6, 123.9, 122.4, 121.6, 121.6, 98.2, 96.3, 94.5, 89.0, 80.1, 73.2, 68.1, 63.2, 61.5, 50.6, 30.0, 29.8, 19.2, 14.5: HRMS calcd. C30H25°6NCs (M+Cs) , 628.0736; found: 628.0750.
Compounds 24a, b, d, a, f and g are similarly prepared.
Alternative Preparation of Compound 5 Toluenesulfonic acid (TsOH.H2O; 8 mg, 0.05 mmol) was added in one portion to a solution of the alcohol Compound 2 (18 mg, 0.045 mmol), 1,4cyclohexadiene (0.2 mL) and benzene (0.5 mL) at 25°C, and the solution was stirred for 24 hours. The organic solvent was removed in vacuo and the residue was purified by flash chromatography to give the ketone Compound 5 (15 mg, 90 percent). (b) Trimethylsilyl trifluoromethylsulfonate (TMSOTf; 15 gL, 0.08 mmol) was added to a solution of the alcohol Compound 2 (32 mg, 0.078 mmol) and triethylsilane (EtjSiH) (40 mg, 0.32 mmol) in CH2C12 (2 mL) at -78°C. After 1 minute, the mixture was quenched at -78°C with saturated NH4C1 solution (1 mL), diluted with ether (10 mL), washed with water (2x3 mL), brine (3 mL) and then dried (MgSO4). The organic solvent was removed in vacuo, and the residue was purified by flash chromatography to give the ketone Compound 5 (22 mg, 75 percent).
Example 23: (a) (c) HC1 gas was bubbled through a solution of the alcohol Compound 2 (32 mg, 0.078 mmol) and 1,4cyclohexadiene (40 mg, 0.32 mmol) in dichloromethane (4 mL) at 25°C for 30 seconds. The solvent was removed in vacuo and the residue was purified by flash chromatography to give the ketone Compound 5 (25 mg, 80 percent). - 125 Example 24: Compound 2b A solution of the phenyl carbamate Compound 2 (42 mg, 0.103 mmol) in dry methanol (4 mL) was treated with sodium methoxide (17 mg, 0.31 mmol) and heated at 60°C for 2 hours. The reaction mixture was diluted with dichloromethane (25 mL), washed with sodium bicarbonate solution (25 mL), dried (Na2SO4) , evaporated in vacuo and the residue purified by flash chromatography (silica, 40 percent ether in petroleum ether) to give methyl carbamate 2b (28.5 mg, 80 percent). 2b: white crystalline solid, mp 126-127°C (from ether/petroleum ether); Rf=0.43 (50 percent ether in petroleum ether); IR (CDC13) 3600, 3450, 2957, 2257, 2250, 1706 cm'1; ’Η NMR (500 MHZ, CDClj): δ 8.65 (d, J=8.0 Hz, 1 H, aromatic), 7.25-7.10 (m, 3 H, aromatic), 5.81 (d, J=10.1 Hz, 1 H, olefinic), 5.69 (d, J=10.1 Hz, 1 H, olefinic), 5.45 (s, 1 H, CH-N), 3.82 (s, 3 H, OMe), 2.79 (s, 1 H, OH), 2.27-1.72 (m, 6 H, CH2) ; 13C NMR (125 MHz, CDClj): 6 135.9, 131.3, 127.8, 127.5, 126.1, 124.9, 123.9, 122.1, 100.7, 94.1, 88.3, 74.2, 73.1, 65.8, 64.2, 53.7, 50.1, .2, 23.2, 19.2, 15.2; MS m/e (relative intensity) 347 (M*, 100) 291 (35), 204 (50) ; HRMS calcd. for C21H17NO4 (M+) 347.1158, found 347.1159. Anal, calcd. for C21H17NO4: C, 72.61; H, 4.93; N, 4.03. Found: C, 72.63; H, 5.24; N, 3.79.
Example 25: Compound 40 Carbamate Compound 21 (39 mg, 0.10 mmol) in THF (3 mL) was treated at zero degrees C with LiAlH4 (0.25 mL of a 1.0 M solution in ether, 0.25 mmol). After stirring for 30 minutes, the reaction was quenched with saturated sodium bicarbonate solution (1 mL), diluted with ether (20 mL), washed with 1.0 M aqueous LiOH solution (2x5 mL) in order to remove phenol, dried (Na2SO4) , filtered and stored under argon at -78°C until - 126 required. MS (FAB+) m/e (relative intensity) 290 (97), 278 (75), 274 (M+H, 98), 235 (100)? HRMS calcd. for C19H16NO (M+H) 274.1232, found 274.1247.
Physical data for further selected compounds: Compound 42 Rf=0.63 (50 percent diethyl ether in benzene)? 1H NMR (300 MHz, d8-THF/D2O, 10:1):6 8.53 (d, J=8.8 Hz, 1 H, aromatic), 7.45-7.10 (m, 5 H, aromatic), 6.88 (dd, J=2.5 Hz, 1 H, aromatic), 6.63 (dd, J=8.8, 2.5 Hz, 1 H, aromatic), 5.97 (d, J=10.0 Hz, 1 H, olefinic), 5.78 (dd, J=10.0, 1.6Hz, 1 H, olefinic), 5.46 (bs, 1 H, CHN), 2.35-1.55 (m, 6 H, CH2) .
Compound 43 Rf=0.78 (50 percent diethyl ether in benzene)? 1H NMR (300 MHz, C6D6) : δ 8.97 (d, J=9.0 Hz, 1 H, aromatic), 7.72 (d, J=8.3 Hz, 1 H, aromatic), 7.52 (d, J=7.7 Hz, 1 H, aromatic), 7.13-7.01 (m, 5 H, aromatic), 6.97-6.87 (m, 2 H, aromatic), 6.81 (bd, J=8.9 Hz, 1 H, aromatic), 6.66 (t, J=7.9 Hz, 1 H, aromatic), 5.90 (bs, H, C HN), 5.31 (d, J=10.1 Hz, 1 H, olefinic), 5.17 (dd, J=10.1, 1.7 Hz, 1 H, olefinic), 5.13 and 5.04 (AB, J=16.0 HZ, 2 H, ArCHjO) , 2.29 (bs, 1 H, OH), 2.15-1.85 (m, 4 H, CH2), 1.70-1.60 (m, 1 H, CH2) , 1.37-1.29 (m, 1 H, CH2)? IR (C6H6) 3554, 2954, 2927, 1728, 1615, 1579, 1529, 1506, 1494, 1378, 1343, 1302, 1280, 1252, 1239, 1202 cm1? HRMS Calcd for C33H25N2O7 (M+H): 561.1162, found 561.1162.
Compound 44c Rf=0.33 (5 percent methanol in methylene chloride)? ’h NMR (300 MHz, CDCl3):ff 7.43 (dd, J=5.3, 3.5 Hz, 1 H, aromatic), 7.25-7.10 (m, 4 H, aromatic), 6.56 (dd, J=8.4, 2.2 Hz, 1 H, aromatic), 6.53 (d, J=2.2 127 Hz, 1 H, aromatic, 5.58 (s, 1 H, CHN), 5.46 (t, J=5.6 HZ, 1 H, CH2NHCON) , 3.19-2.95 (m, 2 H, CH2NHCON) , 2.80 (dt, J=11.3, 6.3 Hz, 1 H, CH2CH2NH) , 2.53-2.26 (m, 5 H, CH2CH2NH, CH2, OH), 1.84 (S, 1 H, OH), 1.68 (dd, J=12.4, 4.7 HZ, 1 H, CH2) , 1.61-1.36 (m, 5 H, CH2CH2NHCON, CH2CH2NH, CH2) , 0.94 (t, J=7.3 Hz, 3 H, CH3CH2CH2NHCON) , 0.89 (dd, J=4.8, 2.4 Hz, 1 H, CH2) , 0.83 (t, J=7.3 Hz, 3 H, CH3CH2CH2NH) , 0.78-0.59 (m, 1 H, CH2) ; IR (CHCl3) 3591, 3439, 3270, 2964, 2935, 1645, 1613, 1500, 1459, 1416, 1252, 1188 cm'1; HRMS Calcd. for C26H34N3O4 (M+H):452.2549, found: 452.2549.
Compound 45 Rf=0.22 (silica, 70 percent diethyl ether in 15 petroleum ether) 1H NMR (500 MHz, CDC13):6 7.92-7.1 (m, 9H, aromatic), 5.73 (d, J=10.1 Hz, 1 H, olefinic), 5.63 (d, J=10.1 Hz, 1 H, olefinic), 5.37 (bs, 1 H, NC H), 4.65-4.22 (m, 2 H, SO2CH2CH2) , 3.73 (S, 1 H, CHCH2) , 3.48 (m, 2H, SO2CH2CH2) , 2.43-1.52 (m, 6 H, CH2) ; 13C NMR (125 MHZ, CDC13) : δ 134.01, 129.3, 128.5, 128.1, 127.9, 127.1, 125.2, 124.8, 121.9, 101.7, 93.7, 91.2, 88.6, 70.1, 60.9, 59.3, 55.0, 49.4, 29.3, 23.1, 22.3, 15.6; IR (CHClj) 2975, 2950, 1715, 1360, 1300, 1150 cm'1; HRMS Calcd. for C28H23SNCs (M+Cs®) :618.0351, found: 618.0352.
Compound 48 Rf=0.61 (silica, 70 percent diethyl ether in petroleum ether) 1H NMR (500 MHz, CDC13):6 8.32 (d, J=7.34 HZ, 1 H, aromatic), 7.11 (t, J=7.34 Hz, IH, aromatic), 6.82 (t, J=7.34 Hz, 1 H, aromatic), 6.55 (d, J-7.34 Hz, 1 H, aromatic), 5.83 (d, J=8.8 Hz, 1 H, olefinic), 5.73 (dd, J=8.8, 1.74 Hz, olefinic), 4.32 (d, J=1.74 Hz, 1 H, NC H), 4.00 (bs, 1 H, NH), 3.50 (s, 3 H, OC H3), 2.36-1.68 (m, 6 H, CH2) ; 13C NMR (125 MHZ, CDC13) : 35 142.2, 131.0, 128.3, 123.1, 122.5, 122.0, 119.3, 115.9, - 128 100.2, 96.9, 94.6, 87.3, 79.6, 72.9, 62.9, 29.0, 24.6, 19.0; IR (CHC13) 3400, 2950, 2850, 1100, 1080 cm'1; HRMS Calcd. for C20H17O2N (^): 303.1337, found 303.1348.
Compound 50 Rf=0.40 (silica, 70 percent diethyl ether in petroleum ether) 1H NMR (500 MHz, CDC13) : S 7.63 (d, J=7.5 Hz, 1 H, aromatic), 7.35 (m, 2 H, aromatic), 7.18 (d, J=7.0 Hz, 1 H, aromatic), 7.14 (t, J=7.0 Hz, 1 H aromatic), 7.09 (t, J=7.0 Hz, 1 H, aromatic), 7.03 (m, 3 H, aromatic), 6.87 (d, J=7.0 Hz, 1 H, aromatic), 6.80 (t, J=7.0 Hz, 1 H, aromatic), 6.61 (t, J=7.0 Hz, 1 H, aromatic), 6.31 (d, J=7.5 Hz, aromatic), 4.12 (2s, 2H, NH and N-CH), 3.73 (s, 1 H, OH), 3.62 (t, J=2.82 Hz, 1 H, CH-CH2) , 2.80 (ddd, J=12.8, 12.8, 5.64 Hz, 1 H, CH2) , 2.41 (ddt, J=12.8, 12.8, 4.5 Hz, 1 H, CH2) , 1.75 (dd, J=13.16, 4.88 Hz, 1 H, CH2) , 1.54 (m, 1 H, CH2) , 1.39 (bd, J=13.16 HZ, 1 H, CH2) , 0.9 (m, 1 H, CH2) ; 13C NMR (125 MHz, CDC13) : 141.6, 139.2, 137.1, 135.1, 133.7, 130.6, 128.1, 127.8, 127.4, 127.0, 126.8, 126.4, 119.9, 115.8, 70.4, 62.1, 55.6, 33.3, 29.8, 28.0, 18.8: IR (CHC13) 3450, 3390, 3070, 2930, 2870, 1490, 1470 cm'1; HRMS Calcd. for C25H23OSN (M+) :385.1500, found 385.1500.
Compound 55 Rf=0.3 (50 percent diethyl ether in petroleum ether); 1H NMR (500 MHz, CDC13) : 5 8.21 (d, J=8.8 Hz, 1 H, aromatic), 7.32 (t, J=7.6 Hz, 2 H, aromatic), 7.18 (t, J=7.6 Hz, 1 H, aromatic), 7.10 (bd, J=6.9 Hz, 2 H, aromatic), 6.89 (bs, 1 H, aromatic), 6.65 (dd, J=8.8, 2.7 Hz, 1 H, aromatic), 5.82 (d, J=10 Hz, 1 H, olefinic), 5.67 (dd,-J=10, 1.7 Hz, 1 H, olefinic), 5.48 (S, 1 H, OH), 5.28 (bs, 1 H, CHN), 3.47 (s, 3H, OCH3) , 2.28 (dd, J=15.1, 8.2 Hz, 1 H, CH2) , 2.15 (m, 2 H, CH2) , 129 1.92 (m, 2 H, CH2) , 1.75 (m, 1 H, CH2) ; 13C NMR (125 MHz, CDClj): S 155.1, 150.9, 136.8, 133.2, 131.0, 130.1, 129.3, 125.8, 124.2, 124.1, 122.2, 121.6, 113.0, 99.5, 94.9, 93.9, 88.4, 79.3, 72.1, 63.2, 52.1, 50.5, 28.5, 23.2, 18.9: IR(CHClj) 3400, 3004, 2979, 2936, 2876, 1719, 1384 cm'1; HRMS Calcd. for C27H21NO5Cs (M+Cs): 572.0474, found 572.0429.
Compound 58 Rf=0.31 (diethyl ether); 1H NMR (500 MHz, CDClj): δ 7.37 (d, J=10.3 Hz, 1 H, olefinic), 6.36 (dd, J=10.4, 2.0 Hz, 1 H, olefinic), 5.85 (d, J=9.8 Hz, 1 H, olefinic), 5.81 (dd, J=1.7 Hz, 1 H, olefinic), 5.10 (d, J=2.0 Hz, 1 H, olefinic), 4.13 (d, J=4.0 Hz, 1 H, NH), 4.07 (d, J=3.0 HZ, H, olefinic), 3.72 (dd, J=4.2, 1.7 Hz, 1 H, CHN) , 3.41 (s, 3H, OCHj) , 3.20 (m, 1 H, CH2) , 2.36 (m, 1 H, CH2) , 2.10 (m, 1 H, CH2) , 1.88 (m, 1 H, CH2) , 1.74 (m, 1 H, CH2) ; 13C NMR (125 MHz, C6D6) : δ 184.4, 157.2, 137.7, 134.8, 123.3, 122.6, 113.3, 98.8, 98.4, 90.7, 87.2, 78.1, 74.8, 74.0, 58.4, 57.8, 51.5, 27.5, 27.4, 14.3; IR(CHClj) 3527, 3385, 2956, 2928, 2855, 1656, 1597 cm'1; UV (CHClj, c=2.2 x 10-4): A(log e) 330 (3.09), 285 (3.37), 256 (3.7), 244 (3.5); HRMS Calcd. for C20H17O4NCs (M+Cs): 468.0212, found 468.0254.
Compound 76 Rf = 0.44 (33 percent ethyl ether in petroleum ether); 1H NMR (300 MHz, CDClj) δ 7.68 (dd, J = 7.8, 1.1 Hz, 1 H, aromatic), 7.52 (br s, 1 H, aromatic), 7.37 (t, J = 7.7 Hz, 2 H, aromatic), 7.30 (dd, J = 7.4, 1.1 Hz, 1 H, aromatic), 7.26-7.13 (m, 8 H, aromatic), 5.61 (s, 1 H, CHN), 3.87 (t, J = 2.8 Hz, 1 H, CH2CH-), 2.49 (dd, J = 15.0, 7.8 Hz, 1 H, CH2) , 2.32-2.19 (m, 1 H, CH2) , 2.08-1.98 (m, 2 H, CH2) , 1.90-1.82 (m, 1 H, CH2) , 1.6835 1.55 (m, 1 H, CH2) ; 13C NMR (125 MHz, CDClj) 6 150.9, 130 135.6, 130.0, 129.2, 129.2, 128.9, 128.8, 128.6, 128.3, 128.3, 128.1, 128.1, 127.7, 127.2, 126.8, 125.6, 125.2, 121.5, 121.5, 96.9, 90.7, 90.6, 88.8, 70.1, 60.7, 49.7, 28.9, 22.7, 22.6, 15.5; UV (EtOH) λΜχ (log e) 282 (3.55), 260 (sh, 3.74), 237-210 (br, 4.36-4.32) nm; HRMS Calcd. for C30H21NO3Cs; 576.0576 (M+Cs©), found 576.0611 (M+Cs®).
Compound 87 Rf = 0.52 (33 percent ethyl ether in petroleum ether); 1H NMR (300 MHz, CDC13) 5 7.75 (s, 1 H, aromatic), 7.73 (s, 1 H, aromatic), 7.72-7.66 (m, 3 H, aromatic), 7.53 (br s, 1 H, aromatic), 7.50-7.42 (m, 2 H, aromatic), 7.38 (t, J = 7.7 Hz, 2 H, aromatic), 7.3015 7.13 (m, 5 H, aromatic), 5.64 (s, 1 H, CHN), 3.92 (br s, H, CH2CH), 2.53 (dd, J = 15.4, 7.5 Hz, 1 H, CH2) , 2.34-2.22 (m, 1 H, CH2) , 2.12-2.00 (m, 2 H, CH2) , 1.91I. 84 (m, 1 H, CH2) , 1.70-1.60 (m, 1 H, CH2) ; 13C NMR (125 MHZ, CDC13) S 150.9, 135.8, 132.3, 131.7, 130.3, 129.3, 129.3, 128.7, 128.4, 128.3, 128.1, 127.7, 127.6, 127.6, 127.3, 127.2, 125.6, 125.2, 123.8, 122.7, 121.5, 96.4, 90.7, 90.5, 88.8, 70.2, 60.8, 49.8, 28.9, 22.7, 22.6, 15.5; HRMS Calcd. for C^H^NOjCs: 626.0732 (M+Cs®), found 626.0732 (M+Cs®).
Compound 89 Rf = 0.53 (50 percent ethyl ether in benzene); 1H NMR (300 MHz, CDCl3) δ 8.40 (s, 1 H, aromatic), 8.23 (s, 1 H, aromatic), 8.22 (s, 1 H, aromatic), 7.99-7.88 (m, 2 H, aromatic), 7.75 (dd, J = 7.7, 1.7 Hz, 1 H, aromatic), 7.54 (s, 1 H, aromatic), 7.50-7.40 (m, 5 H, aromatic), 7.30 (d, J = 7.4 Hz, 3 H, aromatic), 7.147.00 (m, 2 H, aromatic), 6.11 (s, 1 H, CHN), 3.62 (br s, H, CH2CH), 2.46 (dddd, J = 10.8, 10.8, 3.3, 3.3 Hz, 1 H, CH2) , 2.30 (ddd, J = 13.6, 13.6, 6.0 Hz, 1 H, CH2) , 131 1.94 (dd, J = 13.3, 4.6 Hz, 1 H, CH2) , 1.53 (br t, J = 13.5 Hz, 2 H, CH2) , 0.98 (ddddd, J = 13.9, 13.9, 13.9, 4.3, 4.3 Hz, 1 H, CH2) .
Compound 115a Pale yellow oil? Rf- 0.39 (silica, 10 percent methanol in dichloromethane), [a]025 = -87.3° (c = 0.48, CHClj) , ’h NMR, (500MHZ, C6D6) : δ - 8.97 (dd, 1 H, J = 4.2, 0.7 HZ, Dyn-Ar), 7.52 (m, 1 H, Dyn-Ar), 7.41-6.98 (m, 12 H, 11 Ar, propargylic H), 6.98 (dd, 1 H, J - 7.1 7.1 Hz, Dyn-Ar), 5.89 (bs, 1 H, OH), 5.83 (bs, 1 Η, O-N H), 5.78 (s, 1 Η, E-l), 5.28 (d, 1 H, J = 10.0 Hz, vinylic H), 5.10 (dd, 1 H, J = 10.0, 1.7 Hz, vinylic H) 4.58-4.51 (m, 2 H, CH2-Ph) , 4.50 (d, 1 H, J = 7.4, A-1) , 4.48-4.40 (m, 1 H, E-5ax), 4.25-4.17 (m, 1 H, E-5eq), 4.13-4.02 (m, 3 H, A-3, OCH2CH2O), 4.01-3.94 (m, 1 H, OCH2CH2O) , 3.93-3.90 (m, 1 Η, E-3), 3.77 (dd, 1 H, J = 9.5, 7.3 Hz, A-2), 3.69-3.52 (m, 1 H, A-5), 3.26 (s, 3 H, OCH3) , 2.78-2.66 (m, 2 Η, E-4, N-CH2) , 2.65-2.57 (m, 1 H, N-CH2) , 2.47 (dd, 1 H, J - 12.0, 2.2 Hz, E-2eq) , 2.44 (dd, 1 H, J = 9.5, 9.5 Hz, A-4), 2.31 (dd, 1 H, J = 14.5, 6.5 Hz, Dyn-CH2) , 2.04 (d, 1 H, J = 6.7 Hz, DynCH2) , 1.95-1.83 (m, 4 H, CH2) , 1.43 (dd, 1 H, J = 14.5, 9.3 Hz, E-2ax), 1.33 (d, 3 H, J = 6.1 Hz, A-6), 1.04 (t 3 H, J = 6.5 Hz, N-CH2-CH3) ; IR (CHC13) = 2965, 2931, 1733, 1380, 1323, 1146, 1098, 1071 cm'1; HRMS calcd. for C49H55N3°ii (M+CS®) 994.2891; found 994.2904.
Compound 115b Pale yellow oil; Rf = 0.38 (silica, 10 percent methanol in dichloromethane), [a]025 = +125.7° (c= 0.68, CHClj) , 1H NMR (500MHz, C6D6) ; δ = 8.93 (dd, 1 H, J = 4.2, 0.7 Hz, Dyn-Ar), 7.56 (dd, J = 7.4, 1.4 Hz, DynAr), 7.32-7.02 (m, 12 H, 11 Ar, propagylic H), 6.90 (dd, 1 H, J = 7.1, 7.1 Hz, Dyn-Ar), 5.90 (bs, 1 Η, O-N-H), - 132 5.88 (bs, 1 H, OH), 5.82 (s, 1 Η, E-l), 5.29 (d, 1 H, J = 10.2 Hz, vinylic H), 5.11 (dd, 1 H, J = 10.2, 1.7 Hz, vinylic H), 4.56-4.51 (m, 2 H, CH2Ph), 4.49 (dd, 1 H, J = 11.1, 9.0 Hz, E-5ax), 4.48 (d, 1 H, J = 7.4 Hz, A-1), 4.22 -4.17 (m, 2 H, OCH2CH2O) , 4.14 (dd, 1 H, J « 11.1, 4.7 Hz, E-5eq), 4.09 (dd, 1 H, J = 9.5, 9.5 Hz, A-3), 4.06-4.01 (m, 1 H, OCH2CH2O) , 3.93-3.88 (in, 1 H, OCH2CH2O) , 3.87-3.81 (m, 1 Η, E-3), 3.78 (dd, 1 H, J 9.5, 7.1 HZ, A-2), 3.58 (dq, 1 H, J = 9.5, 6.1 Hz, A-5), 3.27 (S, 3 H, OCH3) , 2.84 (ddd, 1 H, J = 9.0, 9.0, 4.7 HZ, E-4), 2.77 (m, 2 H, N-CH2) , 2.54 (dd, 1 H, J = 12.2, 2.5 Hz, E-2eq), 2.42 (dd, 1 H, J = 9.5, 9.5 Hz, A-4), 2.30 (dd, 1 H, J = 14.6, 10.5 Hz, Dyn-CH2) , 2.06 (dd, 1 H, J = 14.6, 7.1 Hz, Dyn-CH2) , 1.97-1.83 (m, 4 H, Dyn15 CH2), 1.51 (dd, 1 H, J = 12.2, 9.2 Hz, E-2ax), 1.33 (d, H, J = 6.1 Hz, A-6), 1.10 (t, 3 H, J = 6.5 Hz, N-CH2CH3) ? IR (CHClj) : = 2962, 2957, 2929, 1733, 1386, 1323, 1146, 1097, 1070 cm'1; HRMS calcd. for C^HjjNjO,, (M+Cs®) 994.2891: found 994.2904.
Although the present invention has now been described in terms of certain preferred embodiments, and exemplified with respect thereto, one skilled in the art will readily appreciate that various modifications, changes, omissions and substitutions may be made without departing from the spirit thereof.

Claims (24)

CLAIMS:
1. A fused ring compound corresponding to the structural formula wherein A is a double or single bond; R 1 is selected from the group consisting of H, C t -C 6 alkyl, phenoxycarbonyl, benzyloxycarbonyl, C 1 -C 6 alkoxycarbonyl, substituted C 1 -C 6 alkoxycarbonyl, 20 and 9-fluorenylmethyloxycarbonyl; R 2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyloxy-C 1 -C 6 alkyl; R 3 is selected from the group consisting 25 of H and C 1 -C 6 alkoxy; R 4 is selected from the group consisting of H, hydroxyl, alkoxy, oxyacetic acid, oxyacetic C 1 -C 6 hydrocarbyl or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazilthiocarbonyl and C 1 -C 6 acyloxy; 30 R 6 and R 7 are each H or together form with the intervening vinylene group form a one, two or three fused aromatic six-membered ring system; W together with the bonded vinylene group forms a substituted aromatic hydrocarbyl ring system 35 containing 1, 2 or 3 six-membered rings such that said 134 fused ring compound contains 3, 4 or 5 fused rings, all but two of which are aromatic, and in which W is joined [a, b] to the nitrogen-containing ring of the structure shown; and A 5 R is hydrogen or methyl, with the proviso that R 8 is hydrogen when W together with the intervening vinylene group is 9,10-dioxoanthra.
2. The fused ring compound according to claim 10 1 wherein R 6 and R 7 are H, or together with the intervening vinylene group form a benzo or naphtho ring system.
3. The fused ring compound according to claim 15 1 wherein said substituted aromatic hydrocarbyl ring system W is selected from the group consisting of a substituted or unsubstituted benzo ring, a substituted or unsubstituted naphtho ring and a substituted 9,10dioxoanthra ring.
4. The fused ring compound according to claim 3 wherein the formed aromatic hydrocarbyl ring system is an otherwise unsubstituted benzo ring. 25 5. The fused ring compound according to claim 3 wherein the formed aromatic hydrocarbyl ring system is a benzo ring substituted at one or two of the remaining positions by a radical selected from the group consisting of hydroxyl, C t -C 6 alkoxy, fi-nitrobenzyloxy, 30 benzyloxy, C^-C^-acyloxy, oxyethanol, oxyacetic acid and halo. 135 6. The fused ring compound according to claim 3 wherein the formed aromatic hydrocarbyl ring system is a naphtho ring having a 4-position radical selected from the group consisting of hydroxyl, ¢,-¾ alkoxy, ¢,-¾
5. Acyloxy, benzyloxy and halo, and radicals at the 5- and 8-positions selected from the group consisting of hydroxyl, ¢,-¾ alkoxy, benzyloxy, ¢,-¾ acyloxy, oxo and halo. 10 7. The fused ring compound according to claim 3 wherein the formed aromatic hydrocarbyl ring system is a 9,10-dioxoanthra ring substituted at one or more of the 4-, 5- and 8-positions by a radical selected from the group consisting of hydroxyl, ¢,-¾ alkoxy, ¢,-¾ 15 acyloxy, and halo.
6. 8. The fused ring compound according to claim 1 wherein A is a single bond. 20 9. A fused ring compound corresponding in structure to the formula wherein A is a double or single bond; 136 R 1 is selected from the group consisting of H, alkyl, phenoxycarbonyl, benzyloxycarbonyl, C.j-C 6 alkoxycarbonyl, substituted ethoxycarbonyl and 9-fluorenylmethyloxycarbonyl; 5 R 2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyl oxy-C,alkyl; R 3 is selected from the group consisting of H and C,,-C 6 alkoxy; 10 R 4 is selected from the group consisting of H, hydroxyl, oxyacetic acid, oxyacetic hydrocarbyl or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazilthiocarbonyl and 0,-C^ acyloxy; R 5 is selected from the group consisting 15 of H, hydroxyl, C,-^ alkoxy, fi-nitrobenzyloxy, benzyloxy, and C.,-C 6 acyloxy; R 6 and R 7 are each H or together form with the intervening vinylene group form a one, two or three fused aromatic six-membered ring system; and 20 R 8 is methyl or hydrogen. 10. The fused ring compound according to claim 9 wherein R 2 , R 3 , R 5 , R 6 and R 7 are H. 25 11. The fused ring compound according to claim 10 wherein R 1 is phenoxycarbonyl, phenylsulfonylethoxycarbonyl or naphthylsulfonylethoxycarbonyl. 30 12. The fused ring compound according to claim 11 wherein R 4 is selected from the group consisting of H, hydroxyl, alkoxy, oxyacetic acid, imidazylthiocarbonyloxy, oxyacetic amide and oxyacetic 0,-C^ hydrocarbyl or benzyl esters. 137 13. A fused ring compound corresponding in structure to the formula wherein R 1 is selected from the group 15 consisting of H, phenylsulfonylethoxycarbonyl, naphthylsulfonylethoxycarbonyl, phenoxycarbonyl and benzyloxycarbonyl; and R 4 is selected from the group consisting of H, hydroxyl, oxyacetic acid, oxyacetic hydrocarbyl 20 or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazilthiocarbonyl and acyloxy. 14. The fused ring compound according to claim 13 wherein R 1 is phenoxycarbonyl, 25 phenylsulfonylethoxycarbonyl or naphthlsulfonylethoxycarbonyl. 15. The fused ring compound according to claim 14 wherein R 4 is selected from the group consisting of 30 H, hydroxyl, and oxyethanol. - 138 16. A fused-ring compound corresponding to the formula 15 wherein R 1 is selected from the group consisting of H, phenoxycarbonyl, benzyloxycarbonyl, phenylsulfonylethoxycarbonyl and naphthylsulfonylethoxycabony; R 4 is selected from the group consisting of 20 H, hydroxyl, oxyacetic acid, oxyacetic amide, oxyacetic hydrocarbyl or benzyl ester and oxyethanol; and R 5 is situated meta or para to the nitogen atom bonded to R 1 and is selected from the group consisting of hydroxyl, alkoxy, benzyloxy, 25 acyloxy, oxyethanol, oxyacetic acid, an oxyacetic hydrocarbyl or benzyloxy ester and p-nitrobenzyloxy. 17. The fused ring compound according to claim 16 wherein R 1 is phenylsulfonylethoxycarbonyl. 18. The fused ring compound according to claim 17 wherein R 4 is H. 19. The fused ring compound according to claim 35 18 wherein R 5 is hydroxyl or 0,-C^ acyloxy. 139 20. A pharmaceutical composition that comprises a DNA-cleaving or cytotoxic amount of a fused ring compound having the structural formula shown below dissolved or dispersed in a physiologically tolerable 5 diluent wherein A is a double or single bond; R 1 is selected from the group consisting of H, alkyl, phenoxycarbonyl, benzyloxycarbonyl, 20 alkoxycarbonyl, substituted C t -C 6 alkoxycarbonyl, and
7. 9-fluorenylmethyloxycarbonyl; R 2 is selected from the group consisting of H, carboxyl, hydroxy lmethyl and carbonyloxy-C,,-C 6 alkyl; R 3 is selected from the group consisting of 25 H and alkoxy; R 4 is selected from the group consisting of H, hydroxyl, C,-C 6 alkoxy, oxyacetic acid, oxyacetic hydrocarbyl or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazilthiocarbonyl and C,-^ acyloxy; 30 R 6 and R 7 are each H or together form with the intervening vinylene group form a one, two or three fused aromatic six-membered ring system; W together with the bonded vinylene group forms a substituted aromatic hydrocarbyl ring system 140 containing 1, 2 or 3 six-membered rings such that said fused ring compound contains 3, 4 or 5 fused rings, all but two of which are aromatic, and in which W is joined [a, b] to the nitrogen-containing ring of the structure 5 shown; and R 8 is hydrogen or methyl, with the proviso that R 8 is hydrogen when W together with the intervening vinylene group is 9,10-dioxoanthra.
8. 10 21. The composition according to claim 20 wherein R 6 and R 7 are H, or together with the intervening group form a benzo or naphtho ring system, and R 2 , R 3 and R 8 are H.
9. 15 22. The composition according to claim 21 wherein said substituted aromatic hydrocarbyl ring system W is selected from the group consisting of a substituted or unsubstituted benzo ring, a substituted or unsubstituted naphtho ring and a substituted
10. 20 9,10-dioxoanthra ring.
11. 23. The composition according to claim 21 wherein the formed aromatic hydrocarbyl ring system is a benzo ring substituted at one or two of the remaining 25 positions by a radical selected from the group consisting of hydroxyl, C,-C 6 alkoxy, benzyloxy, C,-C 6 acyloxy, oxyethanol, oxyacetic acid and halo.
12. 24. The composition according to claim 21 30 wherein A is a single bond.
13. 25. The composition according to claim 21 wherein R 1 is pehnoxylcarbonyl, phenylsulfonylethoxycarbonyl or 35 naphthylsulfonylethoxycarbonyl. 141
14. 26. The composition according to claim 25 wherein W is subsituted or unsubstituted benzo.
15. 27. The composition according to claim 26 5 wherein R 6 and R 7 are both H.
16. 28. The composition according to claim 27 wherein said benzo group, W, is substituted meta or para to the nitrogen atom bonded to R 1 with a moiety selected 10 from the group consisting of hydroxyl, alkoxy, benzyloxy, acyloxy, oxyethanol, oxyacetic acid and an oxyacetic hydrocarbyl ester.
17. 29. A chimeric compound comprised of an 15 aglycone portion bonded to (i) an oligosaccharide portion or (ii) a monoclonal antibody or antibody binding site portion thereof that immunoreacts with target tumor cells, wherein said aglycone poriton is a fused 20 ring compound corresponding to the structural formula wherein A is a double or single bond; 142 R 1 is selected from the group consisting of H, C,-C 6 alkyl, phenoxycarbonyl, benzoxycarbonyl, C,C 6 alkoxy carbonyl, substituted alkoxycarbonyl, and 9-fluorenylmethyloxycarbonyl; 5 R 2 is selected from the group consisting of H, carboxyl, hydroxylmethyl and carbonyloxy-C,-C 6 alkyl; R 3 is selected from the group consisting of H and C.,-C 6 alkoxy? 10 R 4 is selected from the group consisting of H, hydroxyl, alkoxy, oxyacetic acid, oxyacetic C.|-C 6 hydrocarbyl or benzyl ester, oxyacetic amide, oxyethanol, oxyimidazilthiocarbonyl and acyloxy; R 6 and R 7 are each H or together form with 15 the intervening vinylene group form a one, two or three fused aromatic six-membered ring system; W together with the bonded vinylene group forms a substituted aromatic hydrocarbyl ring system containing 1, 2 or 3 six-membered rings such that said 20 fused ring compound contains 3, 4 or 5 fused rings, all but two of which are aromatic, and in which W is joined [a, b] to the nitrogen-containing ring of the structure shown; and R 8 is hydrogen or methyl, with the proviso 25 that R 8 is hydrogen when W together with the intervening vinylene group is 9,10-dioxoanthra; said oligosaccharide portion comprising a sugar moiety selected from the group consisting of ribosyl, deoxyribosyl, fucosyl, glucosyl, galactosyl,
18. 30 N-acetylglucosaminyl, N-acetylgalactasaminyl, a saccharide whose structure is shown below, wherein a wavy line adjacent a bond indicates the position of linkage 143 OMe - 144 said monoclonal antibody or combining site portion thereof being bonded to said fused ring compound aglycone portion through an R 4 oxyacetic acid amide or ester bond or an oxyacetic acid amide or ester bond from 5 W, and said oligosaccharide portion being glycosidically bonded to the aglycone portion through the hydroxyl of an R 4 oxyethanol group or the hydroxyl of an oxyethanolsubstituted W. 10 30. The chimeric compound according to claim 29 wherein A is a single bond, R 2 , R 3 , R 6 , R 7 and R 8 are hydrogen, and W is benzo.
19. 31. The chimeric compound according to claim 15 30 wherein said aglycone portion is bonded to said oligosaccharide portion.
20. 32. The chimeric compound according to claim 31 wherein the glycosidic bond between the aglycone and 20 oligosaccharide portions is formed form an R 4 oxyethanol group.
21. 33. The chimeric compound according to claim 31 wherein R 1 is phenoxycarbonyl, 25 phenylsulfonylethoxycarbonyl or naphthylsulfonylethoxycarbonyl.
22. 34. The chimeric compound according to claim 32 wherein said oligosaccharide portion is selected from 30 the group of oligosaccharides shown. -14535. A fused ring compound as claimed in claim 1, substantially as hereinbefore described and exemplified.
23. 36. A pharmaceutical composition according to claim 20, substantially as hereinbefore described.
24. 37. A chimeric compound as claimed in claim 29, substantially as hereinbefore described and exemplified.
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