CA2143853C - 2-aminoalkyl-5-aminoalkylamino substituted isoquinoindazole-6-(2h)-ones with antitumour activity - Google Patents
2-aminoalkyl-5-aminoalkylamino substituted isoquinoindazole-6-(2h)-ones with antitumour activity Download PDFInfo
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Abstract
This invention is directed to 2-aminoalkyl-5-aminoalkylamino substituted isoquino [8,7,6-cd]
indazole-6-(2H)-ones and to 2-aminoalkyl-5-aminoalkylamino substituted-isoquino [5,6,7-cd] indazole-6(2H)-ones.
These compounds have been shown to have antitumor activity.
indazole-6-(2H)-ones and to 2-aminoalkyl-5-aminoalkylamino substituted-isoquino [5,6,7-cd] indazole-6(2H)-ones.
These compounds have been shown to have antitumor activity.
Description
ISOQUINOINDAZOLE-6(2H)-ONES
BACKGROUND OF TfiE INVENTION
Field of the Invention This invention is directed to azaanthrapyrazoles, namely to 2-aminoalkyl-5-amino-alkylamino substituted isoquino [8,7,6-cd] indazole-6-(2H)-ones and to 2-aminoalkyl-5-aminoalkylamino substituted-isoquino [5,6,7-cd] indazole-6(2H)-ones.
These compounds have been shown to have antitumor activity.
Background Certain 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been reported which show antitumor activity in clinical trials. Of particular interest has been ametantrone, 1,4-bis{[2-(2-hydroxyethylamino) ethyl]amino}anthracene-9,10-dione, and mitoxantrone, 5,8-dihydroxy-1,4-bis{[2-(2-hydroxyethylamino)ethyl]
amino}anthracene-9,10-dione. [Zee-Cheng et al., J. Med.
Chem. 21, 291-4 (1978); Cheng et al., "Progress in Medicinal Chemistry", Ellis, G.P. and West, G.B., eds.;
Elsevier: Amsterdam, 1983, Vol. 20, pp. 83 and references cited therein]. Mitoxantrone is a broad spectrum oncolytic agent, whose activity is similar to that of the anthracycline antibiotic doxorubicin. Clinical trials have demonstrated that mitoxantrone has particularly promising activity in the treatment of advanced breast cancer, acute leukemia and lymphoma [Legha, Drugs of Today, 20, 629 (1984)j. Although animal studies have demonstrated a diminished cardiotoxicity in comparison to doxorubicin, some clinical cardiotoxicity has been observed also with mitoxantrone, mostly in patients previously treated with doxorubicin (R. Stuart Harris et 21~3g5~3 al., Lancet, 219, (1984) and references cited therein).
Ametantrone has been reported to be, in animals, about l0-fold less potent and less cardiotoxic than mitoxantrone. Because a delayed toxicity is observed only with mitoxantrone after administration of the two drugs by the i.p. route to non-tumor bearing rats at equieffective antitumor dosages, it is suggested that the presence of the 5, 8-dihydroxy substitution in mitoxantrone might be implicated in the delayed deaths [Corbett et al., Cancer Chemother. Pharmacol., 6, 161, (1981)].
In addition, both mitoxantrone and ametantrone have a remarkable myelodepressive toxicity and both compounds show cross-resistance to cell histotypes developing resistance against doxorubicin mediated by overexpression of glycoprotein P. Such a resistance, which is named multidrug resistance, involves a number of antitumor antibiotics, among which are amacrine and podophyllotoxinic derivatives, and this resistance is one of the main reasons for therapeutical failures in the treatment of solid tumors with such antibiotics.
In an attempt to overcome the above mentioned drawbacks, some chromophore modified anthracenediones have been prepared. For example, E.P. Patent Application 103,381 discloses 2-aminoalkyl-5-aminoalkylamino substituted anthra [1,9-cd] pyrazol-6(2H)-ones (anthrapyrazoles) which are claimed to have antitumor activity. The antitumor activity of said compounds in a number of preclinical models has been reported by H.D.
Hollis Showalter et al. [J. Med. Chem., 30, 121-131, (1987)]. However, anthrapyrazoles are not devoid of toxic side effects, with severe leukopenia (W.H.O. grade 3 and 4) and neutropenia (W.H.O. grade 4) being dose limiting in phase I and phase II clinical trials with 'the anthra-pyrazole CI-941 [I.E. Smith et al., J. Clin. Oncol. 9, 2141-2147, (1991)]. Moreover, a marked nephrotoxicity is associated with CI-941 treatment in the rat [D. Campling and M.E.C. Bobbins, Nephrotoxicity, Peter H. Dekker Bach editor, pp. 345-352, (1991), New York; see Chemical Abstract 116:294n, (1992)], and these authors suggest that renal injury may be a clinical problem with anthrapyrazole therapy.
Therefore, the search for newer active analogues is still highly desirable.
We have now discovered that the introduction of one nitrogen atom in the position 9 or in the position 8 of the above mentioned anthra [1,9-cd] pyrazol-6(2H)-ones provides 2-aminoalkyl-5-aminoalkylamino substituted isoquino [8, 7, 6-cd]
indazole-6-(2H)-ones and 2-amino-alkyl-5-aminoalkylamino substituted-isoquino [5, 6, 7-cd]
indazole-6(2H)-ones respectively, which are endowed with marked antitumor activity.
BRIEF SLJMMARY OF THE INVENTION
The compounds of the invention have the formula (I):
O trt-t_~
(I) N-N~B
wherein R is hydrogen or hydroxy;
one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R is hydrogen;
A and B are the same or different and are selected from the group of C~-Clo alkyl or [phenylalkyl]; CZ-Clo alkyl having one or two substituents selected from the group consisting of ORl and NR2R3; CZ-Clo alkyl interrupted by one or two oxygen atoms or by one -NR4- group, and said CZ-Clo, alkyl is optionally substituted by one or two hydroxy (OH) or NRZR3 groups;
Rl is selected from the group consisting of hydrogen, C1-C6 _2143353 alkyl, phenyl, [phenylalkyl] , -S (02) R5, C2-C6 alkyl optionally substituted by NR2R3;
RZ and R3 may be the same or different and are selected from the group consisting of hydrogen, C,-C,o alkyl, [phenylalkyl] , phenyl, CZ-C,~, alkyl substituted with one or two hydroxy (OH) groups, or RZ and R3 taken together with the nitrogen atom to which they are bound form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains l0 another heteroatom such as sulfur, oxygen or nitrogen;
R4 is selected from the group consisting of hydrogen, C~-C~~
alkyl, C2-C,~ hydroxyalkyl, Cz-C,o alkyl substituted with NRZR3, [phenylalkyl] , phenyl;
RS is selected from the group consisting of C,-Ci" alkyl, [phenylalkyl], as free bases and their salts with pharmaceutically acceptable acids.
The present invention also concerns the tautomeric forms, the single enantiomers and diastereoisomers of the compounds of formula (I), as well 2o as mixtures thereof.
The present invention also concerns the non-toxic salts of the compounds of formula (I) with acids acceptable for pharmaceutical and veterinary use such as those obtained by addition of inorganic acids such as hydrochloric, hydrobromic, sulfuric, phosphoric, pyrophosphoric acid, and/or of organic acids such as acetic, propionic, citric, benzoic, lactic, malefic, fumaric, succinic, tartaric, glutamic, aspartic, gluconic, ascorbic acids and the like.
DETAILED DESCRIPTION OF THE INVENTION
In compounds (I) the term "phenyl" means phenyl rings which can optionally contain one or two substituents such as C,-C4 alkyl groups, CF3, halogen atoms, vitro, amino, acetylamino, formylamino, dimethylamino, diethylamino, hydroxy, methoxy and ethoxy groups.
_2143853 Preferred examples of C~-C,~ alkyl groups are methyl, ethyl, n-propyl, sec-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl.
Preferred examples of [phenylalkyl] are benzyl 5 and 4-methoxy benzyl. When in compounds of formula (I) A
or B are a Cz-C,~ alkyl interrupted by one or two oxygen atoms or by one -NR4- group and optionally substituted by one or two hydroxy or -NRZR3 groups, at least two carbon atoms are preferably interposed, between said oxygen atoms l0 and/ or the -NR4- and -NRZR3 groups .
When in compounds of formula (I), the -NRZR3 substituent is a 5- or 6-member aromatic or non-aromatic heterocyclic ring which may contain another heteroatom such as sulfur, oxygen and nitrogen, preferred examples of said heterocyclic rings are 1-imidazolyl, 1-pyrrolyl, 1-tetrahydropyrrolyl, 1-pyrazolyl, 4-morpholinyl, 1-piperidinyl, 1-piperazinyl, 1-(4-methyl)-piperazinyl, and 1-(4-benzyl)piperazinyl.
Preferred compounds of the invention are those of formula (I) where R is H and X and Y are as above defined .
Most preferred compounds are those of formula (I) where R is N, X and Y are as above defined, and A and B are independently selected from the group consisting of:
residue of formula - (CHZ) ~,-NHZ wherein p is the integer 2 or 3;
- residue of formula -(CHZ)~,-NR2R3 wherein p is as above defined and RZ and Rj are methyl;
- residue of formula -(CHz)P-NRZR3 wherein p is as above defined and RZ is hydrogen and R3 is methyl;
- residue of formula -(CHZ)P-OH wherein p is as above def fined;
- residue of formula -(CHz)~,-NH-(CHZ)q-OH wherein p and q are independently an integer selected from the group consisting of 2 or 3;
_'2143853 Specific examples of the preferred compounds of this invention are reported in table 1 and have the following chemical names:
(1) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydrox yethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole -6(2H)-one;
(2) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-amino-propyl)amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(3) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-amino-ethyl)amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(4) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(5) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(6) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydro-xyethyl)amino]ethyl]amino]isoquino[5,6,7-cd) indazole-6(2H)-one;
BACKGROUND OF TfiE INVENTION
Field of the Invention This invention is directed to azaanthrapyrazoles, namely to 2-aminoalkyl-5-amino-alkylamino substituted isoquino [8,7,6-cd] indazole-6-(2H)-ones and to 2-aminoalkyl-5-aminoalkylamino substituted-isoquino [5,6,7-cd] indazole-6(2H)-ones.
These compounds have been shown to have antitumor activity.
Background Certain 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been reported which show antitumor activity in clinical trials. Of particular interest has been ametantrone, 1,4-bis{[2-(2-hydroxyethylamino) ethyl]amino}anthracene-9,10-dione, and mitoxantrone, 5,8-dihydroxy-1,4-bis{[2-(2-hydroxyethylamino)ethyl]
amino}anthracene-9,10-dione. [Zee-Cheng et al., J. Med.
Chem. 21, 291-4 (1978); Cheng et al., "Progress in Medicinal Chemistry", Ellis, G.P. and West, G.B., eds.;
Elsevier: Amsterdam, 1983, Vol. 20, pp. 83 and references cited therein]. Mitoxantrone is a broad spectrum oncolytic agent, whose activity is similar to that of the anthracycline antibiotic doxorubicin. Clinical trials have demonstrated that mitoxantrone has particularly promising activity in the treatment of advanced breast cancer, acute leukemia and lymphoma [Legha, Drugs of Today, 20, 629 (1984)j. Although animal studies have demonstrated a diminished cardiotoxicity in comparison to doxorubicin, some clinical cardiotoxicity has been observed also with mitoxantrone, mostly in patients previously treated with doxorubicin (R. Stuart Harris et 21~3g5~3 al., Lancet, 219, (1984) and references cited therein).
Ametantrone has been reported to be, in animals, about l0-fold less potent and less cardiotoxic than mitoxantrone. Because a delayed toxicity is observed only with mitoxantrone after administration of the two drugs by the i.p. route to non-tumor bearing rats at equieffective antitumor dosages, it is suggested that the presence of the 5, 8-dihydroxy substitution in mitoxantrone might be implicated in the delayed deaths [Corbett et al., Cancer Chemother. Pharmacol., 6, 161, (1981)].
In addition, both mitoxantrone and ametantrone have a remarkable myelodepressive toxicity and both compounds show cross-resistance to cell histotypes developing resistance against doxorubicin mediated by overexpression of glycoprotein P. Such a resistance, which is named multidrug resistance, involves a number of antitumor antibiotics, among which are amacrine and podophyllotoxinic derivatives, and this resistance is one of the main reasons for therapeutical failures in the treatment of solid tumors with such antibiotics.
In an attempt to overcome the above mentioned drawbacks, some chromophore modified anthracenediones have been prepared. For example, E.P. Patent Application 103,381 discloses 2-aminoalkyl-5-aminoalkylamino substituted anthra [1,9-cd] pyrazol-6(2H)-ones (anthrapyrazoles) which are claimed to have antitumor activity. The antitumor activity of said compounds in a number of preclinical models has been reported by H.D.
Hollis Showalter et al. [J. Med. Chem., 30, 121-131, (1987)]. However, anthrapyrazoles are not devoid of toxic side effects, with severe leukopenia (W.H.O. grade 3 and 4) and neutropenia (W.H.O. grade 4) being dose limiting in phase I and phase II clinical trials with 'the anthra-pyrazole CI-941 [I.E. Smith et al., J. Clin. Oncol. 9, 2141-2147, (1991)]. Moreover, a marked nephrotoxicity is associated with CI-941 treatment in the rat [D. Campling and M.E.C. Bobbins, Nephrotoxicity, Peter H. Dekker Bach editor, pp. 345-352, (1991), New York; see Chemical Abstract 116:294n, (1992)], and these authors suggest that renal injury may be a clinical problem with anthrapyrazole therapy.
Therefore, the search for newer active analogues is still highly desirable.
We have now discovered that the introduction of one nitrogen atom in the position 9 or in the position 8 of the above mentioned anthra [1,9-cd] pyrazol-6(2H)-ones provides 2-aminoalkyl-5-aminoalkylamino substituted isoquino [8, 7, 6-cd]
indazole-6-(2H)-ones and 2-amino-alkyl-5-aminoalkylamino substituted-isoquino [5, 6, 7-cd]
indazole-6(2H)-ones respectively, which are endowed with marked antitumor activity.
BRIEF SLJMMARY OF THE INVENTION
The compounds of the invention have the formula (I):
O trt-t_~
(I) N-N~B
wherein R is hydrogen or hydroxy;
one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R is hydrogen;
A and B are the same or different and are selected from the group of C~-Clo alkyl or [phenylalkyl]; CZ-Clo alkyl having one or two substituents selected from the group consisting of ORl and NR2R3; CZ-Clo alkyl interrupted by one or two oxygen atoms or by one -NR4- group, and said CZ-Clo, alkyl is optionally substituted by one or two hydroxy (OH) or NRZR3 groups;
Rl is selected from the group consisting of hydrogen, C1-C6 _2143353 alkyl, phenyl, [phenylalkyl] , -S (02) R5, C2-C6 alkyl optionally substituted by NR2R3;
RZ and R3 may be the same or different and are selected from the group consisting of hydrogen, C,-C,o alkyl, [phenylalkyl] , phenyl, CZ-C,~, alkyl substituted with one or two hydroxy (OH) groups, or RZ and R3 taken together with the nitrogen atom to which they are bound form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains l0 another heteroatom such as sulfur, oxygen or nitrogen;
R4 is selected from the group consisting of hydrogen, C~-C~~
alkyl, C2-C,~ hydroxyalkyl, Cz-C,o alkyl substituted with NRZR3, [phenylalkyl] , phenyl;
RS is selected from the group consisting of C,-Ci" alkyl, [phenylalkyl], as free bases and their salts with pharmaceutically acceptable acids.
The present invention also concerns the tautomeric forms, the single enantiomers and diastereoisomers of the compounds of formula (I), as well 2o as mixtures thereof.
The present invention also concerns the non-toxic salts of the compounds of formula (I) with acids acceptable for pharmaceutical and veterinary use such as those obtained by addition of inorganic acids such as hydrochloric, hydrobromic, sulfuric, phosphoric, pyrophosphoric acid, and/or of organic acids such as acetic, propionic, citric, benzoic, lactic, malefic, fumaric, succinic, tartaric, glutamic, aspartic, gluconic, ascorbic acids and the like.
DETAILED DESCRIPTION OF THE INVENTION
In compounds (I) the term "phenyl" means phenyl rings which can optionally contain one or two substituents such as C,-C4 alkyl groups, CF3, halogen atoms, vitro, amino, acetylamino, formylamino, dimethylamino, diethylamino, hydroxy, methoxy and ethoxy groups.
_2143853 Preferred examples of C~-C,~ alkyl groups are methyl, ethyl, n-propyl, sec-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl.
Preferred examples of [phenylalkyl] are benzyl 5 and 4-methoxy benzyl. When in compounds of formula (I) A
or B are a Cz-C,~ alkyl interrupted by one or two oxygen atoms or by one -NR4- group and optionally substituted by one or two hydroxy or -NRZR3 groups, at least two carbon atoms are preferably interposed, between said oxygen atoms l0 and/ or the -NR4- and -NRZR3 groups .
When in compounds of formula (I), the -NRZR3 substituent is a 5- or 6-member aromatic or non-aromatic heterocyclic ring which may contain another heteroatom such as sulfur, oxygen and nitrogen, preferred examples of said heterocyclic rings are 1-imidazolyl, 1-pyrrolyl, 1-tetrahydropyrrolyl, 1-pyrazolyl, 4-morpholinyl, 1-piperidinyl, 1-piperazinyl, 1-(4-methyl)-piperazinyl, and 1-(4-benzyl)piperazinyl.
Preferred compounds of the invention are those of formula (I) where R is H and X and Y are as above defined .
Most preferred compounds are those of formula (I) where R is N, X and Y are as above defined, and A and B are independently selected from the group consisting of:
residue of formula - (CHZ) ~,-NHZ wherein p is the integer 2 or 3;
- residue of formula -(CHZ)~,-NR2R3 wherein p is as above defined and RZ and Rj are methyl;
- residue of formula -(CHz)P-NRZR3 wherein p is as above defined and RZ is hydrogen and R3 is methyl;
- residue of formula -(CHZ)P-OH wherein p is as above def fined;
- residue of formula -(CHz)~,-NH-(CHZ)q-OH wherein p and q are independently an integer selected from the group consisting of 2 or 3;
_'2143853 Specific examples of the preferred compounds of this invention are reported in table 1 and have the following chemical names:
(1) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydrox yethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole -6(2H)-one;
(2) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-amino-propyl)amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(3) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-amino-ethyl)amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(4) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(5) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(6) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydro-xyethyl)amino]ethyl]amino]isoquino[5,6,7-cd) indazole-6(2H)-one;
(7) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-amino propyl) amino]isoquino[5,6,7-cd)indazole-6(2H)-one;
(8) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-aminoethyl) amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(9) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methyl-amino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(10) 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethyl-amino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(11) 5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-(dimethylamino)ethyl]isoquino [8,7,6-cd]indazole-6 (2H)-one;
(12) 5-[(3-aminopropyl)amino]-2-[2-(dimethylamino)ethyl) isoquino [8,7,6-cd]indazole-6(2H)-one;
(13) 5-[(2-aminoethyl)amino]-[2-[2-(dimethylamino) ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
w 2143853 (14) 5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino[8,7,6-cd]indazole-6(2H)-one;
w 2143853 (14) 5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino[8,7,6-cd]indazole-6(2H)-one;
(15) 5-[[2-(dimethylamino)ethyl]amino]-2-[2-(dimethyl-amino)ethyl]isoquino[8,7,6-cd]indazole-6(2fI)-one;
(16) 5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-(di-methylamino)ethyl]isoquino[5,6,7-cd]indazole-6(2H)-one;
(17) 5-[(3-aminopropyl)amino]-2-[2-(dimethylamino) ethyl]isoquino[5,6,7-cd]indazole-6(2H)-one;
(18) 5-[(2-aminoethyl)amino]-[2-(dimethylamino)ethyl]
isoqu~ino [5,6,7-cd]indazole-6(2H)-one;
isoqu~ino [5,6,7-cd]indazole-6(2H)-one;
(19) 5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
(20) 5-[[2-(dimethylamino)ethyl]amino)-2-[2-(dimethyl-amino)ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
(21) 2-[2-aminoethyl]-5-[[2-[(2-hydroxyethyl)amino]ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(22) 2-[2-aminoethyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(23) 2-[2-aminoethyl)-5-[(2-aminoethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(24) 2-[2-aminoethyl]-5-[[2-(methylamino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one;
isoquino[8,7,6-cd]indazole-6(2H)-one;
(25) 2-[2-aminoethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
(26) 2-[3-aminopropyl)-5-[[2-[(2-hydroxyethyl)amino]ethy 1] amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(27) 2-[3-aminopropyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6 (2H)-one;
(28) 2-[3-aminopropyl]-5-[(2-amino)ethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(29) 2-[3-aminopropyl]-5-[[2-(methylamino)ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(30) 2-[3-aminopropyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
(31) 5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[3-aminopropyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
_2143853 (32) 5-[[2-((2-hydroxyeth yl)amino]ethyl]amino]-2-[2-ami.noethyl]isoquino [5,6,7-cd)indazole-6(2H)-one;
_2143853 (32) 5-[[2-((2-hydroxyeth yl)amino]ethyl]amino]-2-[2-ami.noethyl]isoquino [5,6,7-cd)indazole-6(2H)-one;
(33) 2-((2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl) amino]ethyl]amino]isoquino[8,7,6-cd]indazole-6(21i)-one;
(34) 2-[(2-methylamino)ethyl]-5-[(3-aminopropyl)amino]
isoquino[8,7,6-cd]indazole-6(2I~)-one;
isoquino[8,7,6-cd]indazole-6(2I~)-one;
(35) 2-[(2-methylamino)ethyl]-5-[(2-aminoethyl)amino]
isoquino[8,7,6-cd]indazole-6(2H)-one;
isoquino[8,7,6-cd]indazole-6(2H)-one;
(36) 2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
amino]isoquino (8,7,6-cd]indazole-6(2H)-one;
amino]isoquino (8,7,6-cd]indazole-6(2H)-one;
(37) 2-[(2-methylamino)]ethyl]-5-[[2-(dimethylamino) ethyl]amino]isoquino[8,7,6-cd]indazole-6(21i)-one;
(38) 2-[(2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl) amino]ethyl]amino]isoquino[5,6,7-cd]indazole-6(2ti)-one;
(39) 2-[(2-methylarni.no)ethyl)-5-[(3-aminopropyl)amino]
isoquino(5,6,7-cd]indazole-6(211)-one;
isoquino(5,6,7-cd]indazole-6(211)-one;
(40) 2-[(2-meth ylamino)ethyl]-5-[(2-aminoethyl)amino]
isoquino[5,6,7-cd)indazole-6(211)-one;
isoquino[5,6,7-cd)indazole-6(211)-one;
(41) 2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
aminoJisoquino[5,6,7-cd]indazole-6(2H)-one;
aminoJisoquino[5,6,7-cd]indazole-6(2H)-one;
(42) 2-[(2-methylamino)ethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(43) 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino [5,6,7-cd)indazole-6(2(1)-one;
(44) 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino (5,6,7-cd]indazole-6(2H)-one.
NH-A
Yi \
i X
I I
N N~B
C
TABLE 1 (Continued) o. Y X R A B
1 CH N H C"HZCHZNHCHZCHZOH CHZCHZNHCHZCHZOH
2 CH N H CHZCH~CHZNHZ "' 3 CH N H CH~CH2NHz "' 4 CH N H C'HZCHZNHC:H3 "' 5 CH N H C"HZCH~N (CHI) Z "' 6 N CH H C'HzCH2NHC:HzCHZOH CHZCHZNHCHzCH20H
7 N CH H C'HZCH2CHpNII~ "' 8 N CH H t.'HzCH2NH~ ' 9 N CH H C~H~CH2NHCH3 ", 10 N CH H C~'HZCH~N (CH_i) Z "' 11 CH N H C"HZCHZNH('H~CHZOH CHZCHZN (CH3) ~;
12 CH N H C"H2CH~CH~NH2 "' 13 CH N H C'HZCHZNH~ "' 14 CH N H C'HZCHZNHC"H3 "' 15 CH N H CHZCHZN (C'H S ) ~ "' 16 N CH H C'HZCH ZNHCHZCH?OH CH 2CHZN (CH3) a 17 N CH H CHZCH2CHZNHz "' 18 N CH H C'H~CHZNH~ "
19 N CH H CHzCH2NH('H3 ' 20 N CH H t,HZCH~N (C"H,~) Z "' 21 CH N H C"HZCH~NHC'HzCHZOH CHZCHZNHZ
22 CH N H C~H~,CHZCH~N)-IZ "' 23 CH N H C~HZC~HZNH~
24 C~'H N H ('HZCH~NH(~H ~ "' 25 CH N H lv"HZCH~N (C'H.3) ? ' 26 CH N H C"HZt~'H~NIIC'H~CEi20HCHZCHZCHZNHZ
27 CH N H Cl-i2CH~N1-12 "' 29 CH N H C'H~CHZN11CH; "' 30 CH N H C:'H~C.'H~N (C'H,3) ' z 31 N CH H C'HzCH2NHCH~CH20H CHZCHZCHZNHZ
32 N CH H CVHzCH2NH(:'H-~CHZOH CH2CHZNH2 33 CH N H C"HZCH~NH(~H~CHZOH CHZCHZNHCH3 34 CH N H CH~CH~CH~NH~ ' 35 CH N H C'~IZCH~NH~ "
36 CH N H C'li2CH~NHC"H_{
37 CH N N (.'1-i2CH~N (C:H.~) "
Z
38 N CH H C~H~CHZNHCH;CHZOH CHZCHZNHCH3 39 N CH H CH~CH~CH-~f-IZ "
40 N CH H ('HZCH~NH~ "
41 N CH H C'HZCH~NHC'H~ "
42 N CH H C,I12C1-IzN (CHI) 2 "
43 CH N H C'HZCH~N (CH3) z CH3 44 N CH H C'H~CHZN (C~'H~) ~ CH3 The compounds of this invention can be prepared by the process depicted in scheme 1 and involving the reaction (reaction a) of a compound of formula {1II):
R O Z
X .,,' W
5 (IIIa) X = N, Y = C'.H
~( I IIb ) X = CH, Y = N
wherein Z is OTs (OTs being the p-toluenelsulfonyloxy group) or Cl and W is F or Cl, with the proviso that Z and W can not simultaneously be C1, with a hydrazine of formula { IV ):
10 HZN-NH-B' (IV) where B' has the sanue meanings as B is defined in fornmla (I), or B' is a group that can be converted into B by removal of protective groups for the primary or secondary amines aptionally present in B', to give a compound of formula (II):
R p . Z
Y.o W /
f Nw---N~B>
l Ila) X = N, Y = CH
{IIb) X-CH, Y=N
which then is reacted (reaction b) with a compound of formula (V):
HZN--A' ( V ) where A' has the same meanings as A is defined in formula (I), or A' is a group that can be converted into A by removal of protective groups for the primary or secondary amines optionally present in A', to give the compounds of formula (I'):
R O NH_A, y~ \
X\ I ~ ~ , (I ) N N~B, When A' and/or B' are different from A and/or B, compounds of formula (I') are converted to compounds of formula (I) by removal of the protective groups for the primary~and/or secondary amines optionally present in A' and/or B'.
When, if desired, the process depicted in scheme 1 is performed by reacting compounds of formula (IIIa), then the compounds of the invention of formula (Ia) can be obtained where X represents an atom of nitrogen and Y
represents a carbon atom. Alternatively, if desired, by 2o reacting compounds of formula (IIIb), the compounds of formula (Ib) can be obtained.
Protective groups for the primary and/or secondary amines optionally present in A' and/or B' which can advantageously be used for the preparation of compounds of formula (I) are represented by (C~-Cj) acyl-derivatives (preferably acetyl-derivatives), (C,-C4) alkoxycarbonyl-derivatives (preferably. tert-butoxy-carbonyl-derivatives) and by (C~-C,o)aralkyloxycarbonyl-derivatives (preferably benzyloxycarbonyl-derivatives).
w 2143853 In a preferred embodiment of this invention, compounds of formula (I) are prepared by reaction of a compound of formula (III'):
R O OTs Y
I (III') X
O
with a hydrazine of formula (IV) to give a compound of formula (II'):
R O OTs Y / I \ (II') X~ /
N N~B, Compounds of formula (II' ) are then reacted with a compound of formula (V) to give a compound of formula (I'), which step is followed by removal of the protective groups for the primary and secondary amines optionally present in A' and/or B', to give a compound of formula (I) .
In another preferred embodiment of this invention compounds of formula (I) wherein X is C and Y is N are preferably prepared by reaction of a compound of formula (III" ) R O F
(III" ) N\
_21~38~3 with a hydrazine of formula (IV) to give a compound of formula (II" ) I~ N-N'~
l N I I \ (II,.) /
p CI
Compounds of formula (II " ) are then reacted with a compound of formula (V) to give a compound of formula (I'), which step is followed by removal of the protective groups for the primary and secondary amines optionally present in A' and/or B', to give a compound of formula (I) wherein X is C and Y is N.
The reaction of compounds (III) with the hydrazines (IV) can be performed by heating compounds (III) with a stoichiometric amount of hydrazines (IV) or an excess of hydrazines (IV). The reaction is usually performed in an inert solvent such as methylene chloride, chloroform, 1,1,1-trichloroethane, dimethoxyethane, tetrahydrofuran, dimethylsulfoxide, dimethylformamide, pyridine, picoline, and mixtures thereof, or if it is desired, using compound (IV) itself as the solvent, optionally in the presence of an inorganic base such as an alkaline or alkaline-earth carbonate or hydrogen carbonate or an organic base such as a trialkylamine, at a temperature from 0°C to the reflux temperature of the solvent.
Preferably the reaction is carried out in a solvent such as pyridine, tetrahydrofuran, dimethyl-sulfoxide, or N,N,N',N'-tetramethylethylenediamine, using from 2 to l0 equivalents of compound (IV) for 1 equivalent of compound (III), and working at a temperature ranging from 5°C to 50°C.
_2143853 When, in a particular embodiment of this invention, a compound of formula (III') is reacted with a hydrazine of formula (IV), the reaction is preferably performed with a molar ratio between compounds (III) and (IV) of 1:1.05 to 1:1.25 and by using tetrahydrofuran as solvent at a temperature ranging from room temperature to 50°C.
The reaction of the compounds of formula (II) with the compounds of formula (V) can be performed by l0 heating compounds (II) with a stoichiometric amount of amine (V) or an excess of amine (V). The reaction is usually performed in an inert solvent such as methylene chloride, chloroform, 1,1,1-trichloroethane, dimethoxyethane, tetrahydrofuran, dimethylsulfoxide, dimethylformamide, pyridine, picoline, and mixtures thereof, or, if it is desired, using compound (V) itself as the solvent, optionally in the presence of an inorganic base such as an alkaline or alkaline-earth carbonate or hydrogen carbonate or an organic base such as a trialkylamine, at a temperature from 0°C to the reflux temperature of the solvent.
Preferably the reaction is carried out in a solvent such as pyridine, chloroform, or dimethyl-sulfoxide, using from 2 to 10 equivalents of compound (V) for 1 equivalent of compound (II), and working at a temperature ranging from room temperature to 100°C.
When, in the compounds of formula (I'), A' and/or B' are different from A and/or B, the removal of the protective group for the primary and/or secondary amino functions is carried out following the procedures well known to those skilled in the art. Useful teachings can be found in Green, T.W., Wuts, P.G.M., "Protective Groups in Organic Synthesis", second Edition, John Wiley & Sons, 1991.
For example, the removal of the N-(tert-butoxycarbonyl) protective group can be performed by treatment of a compound of formula (I') with an excess of anhydrous hydrochloric acid in a solvent such as a (C,-C4) alkanol, dichloromethane, chloroform, or mixtures thereof, at a temperature of 0°C to the reflux temperature of the solvent and for a time ranging from several minutes to a few hours. Preferably the reaction is performed in 5 ethanol or in chloroform using from 10 to 20 molar equivalents of anhydrous hydrochloric acid at a temperature of from 20°C to 50°C, and is generally complete in four hours.
The compounds of formula (IV) are known or they 10 can be prepared according to known procedures, see for example, J. Med. Chem., 7, 493, (1964) and J. Het. Chem., 26, 85, (1989).
The compounds of formula (V) are known and commercially available, or they can be prepared according 15 to known procedures. r'or example, the preparation of some N-(tert-butoxycarbonyl) alkanediamines useful for the preparation of some compounds of the present invention is described in Synth. Comm., 20, 2559, (1990) or in J. Med.
Chem., 33, 97, (1990).
The compounds of formula (III) wherein Z = OTs [ compounds III' ) ) an be prepared by a multistep procedure, depicted in scheme 2, involving the following reactions:
(c) the Friedel and Craft acylation of 1,4-difluorobenzene with pyridine-3,4-dicarboxylic anhydrides (VI) where R6 is hydrogen or a suitable protecting group of the hydroxy function such as methoxy or benzyloxy, in presence of A1C13 (110°C, 22 h) which leads to the regioisomeric keto-acids (VIIa) and (VIIb);
(d) reaction of the ketoacids (VIIa) and (VIIb) with sodium methoxide in methanol (8.5 h, reflux) leading to the regioisomeric methoxy-substituted ketoacids (VIIIa) and (VIIIb); compounds (VIIIa) and (VIIIb) where R6 is hydrogen can be reacted as such in the following step;
when R6 is different from hydrogen, compound (VIIIa) is purified by crystallization and reacted as pure regioisomer;
. 2143853 (e) reduction of compounds (VIIIa) (R6 different from hydrogen) with Zn/Cu couple in 75% aqueous formic acid (15' room temperature, then 80°C, 2h) leading to (IX); when R6 is hydrogen, the acids (IXa) and (IXb) can be separated by chromatography yielding the pure isolated regioisomers (IXa) and (IXb);
(f) cyclization of the appropriate acid (IX) by heating a suspension of the compound in polyphosphoric acid at 110-120°C for 2 h leading to the benzo[g]isoquinoline (X);
(g) oxidation of the compound (X) to the corresponding dione (XI) by cerium ammonium nitrate in a mixture of acetonitrile and water (60°C, 2 h);
(h) removal of the methoxy group of the dione (XI) by aluminum chloride in methylene chloride (room temperature 2 h, then ref lux temperature 1. 5 h) leading to compounds (XII) which correspond to a mixture of 9-fluoro 6-hydroxy and 9-chloro-6-hydroxy-5,10-diones (XII) due to partial substitution of the leaving fluoride by means of A1C13; and (i) the final functionalization of the free hydroxy group of (XII) by means of toluenesulfonyl chloride in pyridine at room temperature, leads to the desired compounds ( I I I ) wherein Z = OTs [ compounds ( II I ) ] ;
when R6 is a protective group of the hydroxy function, it can be removed according to methods well known to the expert in the art, thus leading to compound (III) where R
is OH.
In a preferred embodiment of this invention, the preparation of intermediates (XI) is carried out by a multistep procedure depicted in scheme 3 and involving the following reactions:
- cyclization of the mixture of the regioisomeric keto-acids (VIIa) and (VIIb) with 20% oleum at 130-140°C to give the 6,9-difluorobenzo[g]isoquinolines (XIII);
- reaction of (XIII) with one equivalent of sodium methylate in a solvent such as methanol to give a mixture of intermediates (XI) which is separated into the single pure compounds (XIa) and (XIb) by recrystallization from a solvent and/or column chromatography. The pure intermediates (XIa) and (XIb) are then processed according to equation (h) and (i) of scheme 2 and then according to scheme 1 to give compounds (Ia) and (Ib), respectively.
In the preferred process of this invention which provides the compounds of formula (I) wherein X = C and Y = N, the 9-chloro-6-fluorobenzo[g]isoquinoline-5,10 diones of formula (III") are prepared by the multistep process depicted in scheme 4 and involving the following reactions:
- lithiation of 1-chloro-4-fluorobenzene with an alkyllithium reagent such as sec-butyllithium in THF
at -75°C to give 1-lithio-5-chloro-2-fluorobenzene (XIV);
- acylation of 1-lithio-5-chloro-2-fluorobenzene (XIV), generated in situ according to the above step, with pyridine-3,4-dicarboxylic anhydrides (VI) to give the mixture of keto-acids (XVa) and (XVb) which can be separated into the single pure compounds by recrystallization from a solvent or by sublimation;
- reduction of the pure keto-acid (XVa) with Zn/Cu couple or Zn powder in 75% aqueous formic acid (15' at room temperature, then 80°C, 2 hrs) leading to (XVI);
- oxidative cyclization of (XVI) with fuming sulfuric acid (20-30% SO3, 10', 130°C) to give the 9-chloro-6-fluorobenzo[g] isoquinoline-5,10-diones of formula (III'!).
. . , v 2i43s~~
Intermediates (III ") are then processed according to scheme 1 to give the compounds of formula (I) wherein X = C and Y = N.
BIOLOGICAL ACTIVITY OF COMPOUNDS OF THE INVENTION
The evaluation of the biological activity for the compounds of this invention was performed in vitro and in vivo following the protocols developed by the U.S.
National Cancer Institute.
The evaluation of the in vitro cytotoxic activity of the compounds of the invention was performed using a human colon adenocarcinoma cell line (Lovo) isolated from a metastatic nodule, and a subline expressing multidrug resistance. The subline is resistant to a number of antitumor agents, among which are doxorubicin, VP-16, and vincristine. This subline (named Lovo/DX) shows reduced accumulation of doxorubicin and overexpression of a protein (Grandi, M., Geroni, C., Giuliani, F.C., British J. Cancer, (1986), 54, 515). The compounds were tested according to the MTT assay (Mosman, T. "Rapid Colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assay", J. Immunol. Methods, (1983), 65, 55-63; Green, L.M., "Rapid colorimetric assay for cell viability;
application to the quantitation of cytotoxic and growth inhibitory lymphokines", J. Immunol. Methods, (1984), 70, 257-268) in comparison with mitoxantrone, and doxorubicin.
_143853 ICso (~9/ml) com ound LOVO LOVO/DX RI
_. O NH~N~CH~s 0.3 5.0 16.7 I I
N
I
N-N
Nliz O NH~NH~ 0.5 22.4 44.8 I
N-N
N(Ch4s)~
O NH~N(CH~)Z .5 ~ 0.9 1.8 i I I
N
I
N-N~N(CH~)i MITOXANTRONE Q,p4 0.9 22.5 DOXORUBICIN 0.9 66.6 74 In general, representative compounds of this invention were more cytotoxic than doxorubicin and as cytotoxic as mitoxantrone in the Lovo cell line. When mitoxantrone was tested in the Lovo/DX cell line, a resistance index RI (defined a the ratio of the ICS for the resistant line cell to the ICso for the sensitive cell line) as high as 22.5 was found, showing that this subline l0 does have an acquired resistance to mitoxantrone and ametantrone. On the other hand, some compounds of this invention, when tested in the same resistant subline, show no cross resistance with mitoxantrone and ametantrone as reported in Table 2. The in vitro evaluation of representative compounds of this invention suggests that representative compounds of this invention may be useful in order to overcome the multidrug resistance-mediated mechanism of tumor resistance.
~I43~53 Studies of the biological activity in vivo of representative compounds of the invention were performed using the P388 and L1210 marine leukemia models. P388 marine leukemia cells were intraperitoneally (ip) or 5 intravenously (iv) injected in CD2F1 mice. Treatment was initiated approximately 24 hours after tumor transplantation and dosages of the drug were administered ip (P388 ip/ip) or iv (P388 iv/iv) according to preestablished protocols, usually at 3-day (P388 iv/iv) or 10 4-day (P388 ip/ip) intervals. The studies were done over a 60-day period and the date of death for each animal was recorded. The % T/C was determined using the mean survival time (MST) for each group according to the formula ' 15 % T/C = [(MST treated) / (MST control)] x 100 Representative compounds of this invention were able to increase the survival time of treated animals significantly more than mitoxantrone, leading to higher T/C % values at well tolerated dosages. Moreover, the 20 above representative compounds of the invention showed antileukemic activity over a wide range of well tolerated dosages, and, in particular, were active at dosages which were lower than the maximum tolerated dose, providing indication for more favorable therapeutic index in comparison to mitoxantrone.
The antitumor activity of representative compounds of this invention was evaluated also in the L1210 marine leukemia model.
L1210 leukemia cells were intraperitoneally (ip) or intravenously (iv) injected in CDF1 mice and treatment was initiated approximately 24 hours after tumor transplantation. Dosages of the drugs were administered ip (L1210 ip/ip) or iv (L1210 iv/iv) according to preestablished protocols, usually at 3-day (L1210 iv/iv) or 4-day (L1210 ip/ip) intervals. The studies were done over a 60-day period and the date of death for each animal was recorded. The % T/C was determined using the mean survival timed (MST) for each group according to the formula:
% T/C [(MST treated) / (MST control)] x 100 Also in this further leukemia model, representative compounds of this invention showed activity superior to the clinically used antitumor drug mitoxantrone. Since representative compounds of this invention show good results against in vivo models of murine P388 and L1210 leukemias, which are considered to be predictive of antitumor activity in humans, the compounds disclosed herein are expected to be operative against human leukemias and solid tumors sensitive to treatment with antitumor antibiotics.
The compounds of the present invention may therefore be used as active ingredients of therapeutic compositions to induce regression and/or palliation of cancers in mammals when administered in amounts ranging from about 1 mg to about 0.4 g per kilogram of body weight. A preferred dosage regimen would be-from about 1 mg to about 50 mg per kilogram of body weight per day.
Unit dosage may be employed so that from about 70 mg to about 3.5 g of the active compound for a subject of about 70 kg of body weight are administered in a 24-hour period.
The dosage may be adjusted to be compatible to other treatment regimens, such as radiation therapy.
The pharmaceutical composition may be in the form of tablets, capsules, gel capsules, suppositories, lyophilized powders and solutions for intravenous administration. The invention is illustrated by the following non-limiting examples, and variations which are readily apparent to those skilled in the art.
21438.x:3 SYNTHESIS OF COMPOUNDS OF THE INVENTION
Preparative Example 1 Pyridine-3,4-dicarboxylic acid anhydride A mixture of pyridine 3,4-dicarboxylic acid (15.0 g) and acetic anhydride (30 mL) is refluxed for two hours. The excess acetic anhydride is removed by distillation and the anhydride is collected and purified by sublimation (123°C at 3 mm Hg) to yield pyridine 3, 4-dicarboxylic acid anhydride as a white solid ( 10. 1 g) .
m.p.. 74-76°C.
~H-NMR (CDC13): 7.94 (d, 1H); 9.24 (d, 1H); 9.39 (s, 1H).
Preparative Example 2 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl) isonicotinic acid A mixture of pyridine 3,4-dicarboxylic acid anhydride (5.0 g) and aluminum chloride (17.5 g) in 1,4-difluorobenzene (65 mL) is heated in an oil bath at 110°C
for 22 hours. The excess 1,4-difluorobenzene is recovered by distillation. The residue is cooled in an ice-bath and quenched with ice-water (75 mL) and concentrated hydrochloric acid (6.3 mL). The precipitated solid is filtered and dried to yield an approximately 4/1 mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl) isonicotinic acid respectively, as a white powder (7.7 g) which can be recrystallized from acetonitrile and water.
m.p.. 214-217°C.
'H-NMR (DMSO-db): 7.4 (m); 7.5 (m); 7.90 (m); 8.80 (d);
8.90 (d); 9.15 (s).
Recrystallization of this material (15.97 g) from absolute ethanol (360 mL) yields almost pure 3-(2,5-difluoro-benzoyl) isonicotinic acid (1.146 g).
_2143853 Preparative Example 3 4-(2-methoxy-5-fluorobenzoyl)nicotinic acid and 3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid The mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)isonicotinic acid of Preparative Example 2 (14.1 g) is added to a solution of sodium methylate, prepared by portionwise addition of sodium ( 6. 8 g) to dry methanol v ( 140 mL) . The reaction mixture is allowed to react at the reflux temperature for 8.5 hours and at room temperature overnight. The reaction mixture is concentrated to about one third of its volume, water (100 mL) is added and the remaining methanol is removed by distillation. Concentrated HC1 (25 mL) is slowly added to the residue while cooling at 10°C and the obtained precipitate is recovered by suction and washed with 0.1 N HC1, to give an approximately 4:1 mixture of 4-(2-methoxy-5-fluorobenzoyl) nicotinic acid and 3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid (11.31 g).
m.p.. > 230°C.
'H-NMR (DMSO-db): 3.40 (s); 3.45 (s); 7.15 (m); 7.37 (d);
7.42-7.63 (m); 7.26 (d); 8.60 (s); 8.83 (d); 9.07 (s), 13.55 (br.s).
Preparative Example 4 4-(2-methoxy-5-fluorobenzyl)nicotinic acid (and 3-(2-methoxy-5-fluorobenzyl)isonicotinic acid) Zinc-copper couple (L. F. Fieser and M. Fieser, Reagents for Organic Synthesis, Vol. 1, page 1292) (1.5 g) is added to a stirred suspension of the mixture of 4-(2-methoxy-5-fluorobenzoyl)nicotinic acid and3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid of Preparative Example 3 (1.222 g) in formic acid (15 mL) and water (5 mL). After 15 minutes at room temperature the reaction mixture is heated for two hours in a oil bath held at 80°C. After cooling to room temperature the reaction mixture is . _2143853 filtered through a sintered glass filter and the solids are thoroughly washed with 75% aqueous formic acid ( 10 mL) and then with ethyl acetate (10 mL). The combined filtrates are concentrated to about 5 mL, treated with 0.5N HC1 (15 mL) and extracted with ethyl acetate (3 x 20 mL); finally they are saturated with sodium chloride and further extracted with ethyl acetate/1,2-dimethoxyethane 3/1 (2 x 20 mL). The combined organic phases are dried over anhydrous sodium sulphate and the l0 solvent removed under reduced pressure to give a yellowish residue. Subjecting this material to silica-gel column chromatography (eluant: ethyl acetate/methanol/acetic acid from 96/4/0 to 90/10/1 v/v/v) 4-(2-methoxy-5-fluorobenzyl) nicotinic acid (0.805 g) is obtained as a yellowish white solid.
m.p.. > 220°C.
~H-NMR (DMSO-db): 3.70 (s, 3H); 4.33 (s, 2H); 6.91-7.12 (m, 3H); 7.21 (d, 1H); 8.61 (d, 1H); 8.97 (s, 1H). From the above column-chromatography some 3-(2-methoxy-5-fluoro-benzyl)isonicotinic acid may also be recovered.
Preparative Example 5 9-fluoro-10-hydroxy-6-methoxybenzo[g]isoquinoline A mixture of 4-(2-methoxy-5-fluorobenzyl) nicotinic acid (0.63 g) and polyphosphoric acid (15 g) is heated at 110-120°C for two hours under stirring. The heating is removed and water (50 mL) is added to the reaction mixture while it is still warm (60°C). The mixture is cooled to 0°C, neutralized with 20% sodium hydroxide and allowed to stir at room temperature for 1.5 hours; finally it is extracted with 4% methanol in chloroform (4 x 75 mL). The combined organic phases are washed with brine, dried over anhydrous sodium sulphate and the solvents removed under reduced pressure to give 9-fluoro- 10-hydroxy-6-methoxybenzo[g] isoquinoline (0.40 g) as a purple-red solid.
m.p.. > 210°C (from ethanol).
.. . _2143853 ~H-NMR (DMSO-db) :3 .87 (s, 3H) ; 6.70-6.83 (m, 2H) ; 6.92-7.00 (m, 1H); 7.30 (d, 1H); 7.50 (d, 1H); 8.75 (s, 1H); 12.30 (br.s, 1H).
UV (ethanol) : lambda max. (nm) (E ,%) (cm) : 539 (204) ;
5 398 (513); 378 (452); 266 (1232).
IR (KBr): 729, 1245, 1499, 1528, 1620, 1644, and 2838 cm'.
Preparative Example 6 9-fluoro-6-methoxybenzo[g]isoquinoline-5,10-dione A solution of cerium ammonium nitrate (CAN;
10 13.70 g) in water (50 mL) is added during twenty minutes to a stirred suspension of 9-fluoro-10-hydroxy-6-methoxy-benzo[g]isoquinoline (1.22 g) in acetonitrile (150 mL).
At the end of the addition the obtained suspension is heated at 60°C for two hours to give a clear, dark 15 solution which is cooled to room temperature and diluted with water (100 mL). Following removal of acetonitrile by distillation at reduced pressure the aqueous phase is saturated with sodium chloride and extracted with methylene chloride (3 x 150 mL). The combined organic 2o solutions are dried over anhydrous sodium sulphate and the solvent is removed at reduced pressure. The obtained residue is purified by silica-gel column chromatography (eluant: methylene chloride/ethyl acetate from 85/15 to 75/25 v/v) to give 9-fluoro-6-methoxybenzo[g]
25 isoquinoline5,10-dione as a brown-yellow solid (0.48 g).
m.p.. > 220°C.
'H-NMR (CDC13) : 4.05 (s, 3H) ; 7.38 (dd, J=3.39, 9.39 Hz, 1H); 7.55 (dd, J=10.37, 9.39 Hz, 1H), 8.00 (dd, J=5.09, 0.78 Hz, 1H); 9.07 (d, J=5.09 Hz, 1H); 9.45 (d, J=0, 78 Hz, 1 H).
Preparative Example 7 6,9-difluorobenzo[g]isoquinoline-5,10-dione A solution of the mixture of 4-(2,5-difluoro-benzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)iso-nicotinic acid of Preparative Example 2 (61.07 g) in 20%
oleum (100 mL) is heated at 140°C while 20% oleum is added in four portions (13.2 mL each) at 20 min-intervals.
After the fourth addition the mixture is heated for 20 l0 min, then it is cooled to room temperature and quenched with a mixture of ice (1,500 g), water (1,500 mL) and 35%
NaOH (350 mL). The mixture is extracted four times with methylene chloride (1 x 1,000 mL followed by 3 x 500 mL).
The combined organic solutions are washed with water (2 x 1,000 mL), dried (NazS04) and the solvent removed by roto-evaporation. The dark-red solid obtained (56.0 g) is dissolved in boiling THF (840 mL) and decolorizing charcoal (8.40 g) is added. After 30 min the mixture is filtered while hot and the filtrate concentrated to ~20 200 mL. The precipitate obtained is collected by suction filtration to give 6,9-difluorobenzo[g]isoquinoline-5,10-dione (43.00 g) .
m.p.. 201-203°C.
Concentration of the mother liquor to 70 mL yields a second crop of product (3.35 g), m.p. 200-202°C.
Preparative Example 8 9-fluoro-6-methoxybenzo[g]isoquinoline-5,10-dione and 6-fluoro-9-methoxybenzo[g]isoquinoline-5,10-dione A solution of sodium methylate is prepared under a nitrogen atmosphere in a dropping addition funnel from dry methanol (97.6 mL) and sodium (2.024 g) portionwise added. When all the sodium disappears the solution is dropped during 2 h, 35 min to a stirred solution of 6,9-difluorobenzo[g]isoquinoline-5,10-dione of Preparative Example 7 (19.615 g) in dry THF (883 mL) at 20°C. At the end of the addition the solution is concentrated to half its volume by roto-evaporation, then it is cooled to 18°C
for 30 min. The solid which separates is recovered by suction filtration and washed with THF (100 mL); then it is suspended in water (80 mL) under stirring overnight and filtered again to give the solid A (7.4 g).
The mother THF solution is concentrated to dryness. The obtained solid is suspended in water (78 mL) under stirring for 1 hour and filtered to give the solid B (12.9 g).
The solid A (9.30 g) in methylene chloride (45 mL) is heated to reflux for 30 min. After cooling to room temperature the solid is recovered by suction filtration, washed with methylene chloride (5 x 3 mL) and dried under vacuum at 40°C to give 6-methoxy-9-fluorobenzo[g)iso-quinoline-5,10-dione (8.65 g) as a pure compound.
m.p.. 248-250°C.
~H-NMR (CDC13) : 4.05 (s, 3H) ; 7.40 (dd (J=9.39, 3.91 Hz) 1H); 7.55 (dd, J=10.37, 9.39 Hz, 1H); 8.00 (dd, J=5.09, 0.78 Hz, 1H); 9.05 (d, J=5.09 Hz, 1H); 9.48 (d, J=0.78 Hz, 1H) .
The solid B (14.0 g) is dissolved in methylene chloride (140 mL) and the insoluble portion is removed by filtration. The methylene chloride solution is applied on a silica gel (630 g) column chromatography, which is eluted at ambient pressure with methylene chloride. When the yellow chromatographic bands appear well separated the column is eluted with mixtures of methylene chloride/ethyl acetate from 10/1 to 8/2, to 1/1 to give a 94/6 mixture (HPLC evaluation) of 9-methoxy-6-fluorobenzo[g] iso-quinoline-5,10-dione and 6-methoxy-9-fluorobenzo[g] iso-quinoline-5,10-dione respectively (6.50 g).
m.p.. 168-170°C.
~~ 2143853 Preparative Example 9 a) 9-fluoro-6-hydroxybenzo[gJisoquinoline-5,10-dioneand 9-chloro-6-hydroxybenzo[g]isoqu:inoline-5,10-dione (1/1 mixture: small scale reaction) A mixture of 9-fluoro-6-methoxybenzo[gJ iso-quinoline-5,10- dione (0.072 g) and aluminum trichloride (0.112 g) in dry methylene chloride (40 mL) is stirred at room temperature for 4 hours under a nitrogen atmosphere.
An additional portion of aluminum chloride (0.190 g) is l0 added and the mixture is allowed to react at reflux for 1.5 hrs and at room temperature overnight. Following addition of brine (15 mL) the aqueous phase is separated and extracted with methylene chloride (3 x 5 mL). The combined organic solutions are dried over anhydrous sodium sulphate and the solvent is removed by distillation at reduced pressure to give an approximately 1:1 mixture (0.070 g) of 9-fluoro-6-hydroxybenzo[g] isoquinoline-5,10-dione (slower moving yellow spot on silica gel TLC
plate, eluant methylene chloride/ethyl acetate 70/30) and 9-chloro-6-hydroxybenzo [g]isoquinoline-5,10-dione (faster moving yellow spot on the above chromatographic system) which is used without further purification for the next step.
9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione has the following 'H-NMR spectrum (CDC13):
7.38 (dd, 1H); 7.53 (dd, 1H); 8.09 (dd, 1H); 9.15 (d, 1H);
9.57 (d, 1H); 12.56 (s, 1H).
9-chloro-6-hydroxybenzo[g]isoquinoline-5, 10-dione has the following 'H-NMR spectrum (CDC13) :
7.91 (d, 1H); 7.75 (d, 1H); 8.07 (dd, 1H); 9.13 (d, 1H); 9.58 (d, 1H); 12.95 (s, 1H).
_2143853 b) 9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneand 9-chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione(9/1 mixture: multigram preparation):
Aluminum chloride (19.05 g) is added in one portion to a stirred refluxing solution of 6-methoxy-9-fluorobenzo(g]isoquinoline-5,10-dione (7.20 g) in methylene chloride (432 mL). After refluxing for 4 hours the reaction mixture is cooled and poured in water (1,300 mL). Methylene chloride (200 mL) is added and after l0 stirring for 10 min the organic phase is separated. The aqueous solution is saturated with NaCl and further extracted with methylene chloride (3 x 400 mL). The combined organic solutions are washed with brine (1,000 mL), dried and the solvent removed by roto-evaporation.
The brown solid obtained (6.5 g) is recrystallized from ethyl acetate/n-hexane 1/1 (65 mL) to yield a 9/1 mixture ('H-NMR evaluation) of 9-fluoro-6-hydroxybenzo[g] iso-quinoline-5,10-dione and 9-chloro-6-hydroxybenzo[g] iso-quinoline-5,10-dione respectively (6.00 g).
m.p.. partial melting at 179-181°C; complete melting at 193-195°C.
Preparative Example 10 a) 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline 5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]isoquinoline-5,10-dione (1/1 mixture; small scale preparation) The 1:1 mixture of 9-fluoro-6-hydroxybenzo[g]
isoquinoline- 5,10-dione and 9-chloro-6-hydroxybenzo[g]
isoquinoline-5,10-dione, of Preparative Example 9a, (0.060 g) is dissolved in dry pyridine (2 mL) and p-toluene-sulfonyl chloride (0.095 g) is added. After stirring at room temperature for one hour, triethylamine (0.25 mL) is added and stirring is continued for one additional hour.
The reaction mixture is concentrated almost to dryness and . . 2143853 partitioned between 1 N HC1 ( 4 mL) -20% ammonium sulfate ( 6 mL) and ethyl acetate (l0 mL). The aqueous phase is separated, extracted with ethyl acetate (3 x 5 mL) and discarded. The combined organic solutions are dried over 5 anhydrous sodium sulphate and concentrated to dryness to give an approximately 1:1 mixture (0.095 g) of 9-fluoro-6-(p-toluenesulfonyloxy) benzo[g) isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]iso-quinoline-5,10-dione which is used without further 10 purification for the next step.
The pure single compounds can be obtained by silica-gel column chromatography of this mixture (eluant:methylene chloride/n-hexane/ethyl acetate from 50/45/5 to 50/40/10 v/v/v) and they have the following 15 analytical data:
9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]iso-quinoline-5,10-dione: m.p. 173-174°C.
~H-NMR (CDC13): 2.45 (s, 3H), 7.35 (d, 2H); 7.50-7.57 (m, 2H); 7.82-7.94 (m, 3H); 9.08 (d, 1H); 9.48 (s, 1H).
20 9-chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5, 10-dione:
m.p.. 180-181°C.
~H-NMR (CDC13): 2.45 (s, 3H); 7.35 (d, 2H); 7.47 (d, 1H);
7.78-7.91 (m, 4H), 9.07 (d, 1H); 9.48 (s, 1H).
25 b) 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g)isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo [g)isoquinoline -5,10-dione (9/1 mixture; multigram preparation):
Triethylamine (8.20 mL) is added to a stirred 30 suspension of the 9/1 mixture of 9-fluoro-6-hydroxy-benzo[g]isoquinoline-5,10-dione and 9-chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione respectively of Preparative Example 9b (5.53 g) and p-toluenesulfonyl-chloride (8.47 mL) in methylene chloride (166 mL). The reddish-violet solution obtained is left at room temperature under a nitrogen atmosphere for 1 hour and then it is poured into water (500 mL). The organic phase is separated and the aqueous solution is further extracted with methylene chloride (100 mL). The combined organic solutions are dried (NazS04) and concentrated to dryness.
The obtained solid is suspended in n-hexane (100 mL) for 1 hour and filtered to give a 9:1 mixture (~H-NMR
evaluation) of 9-fluoro-G-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluene sulfonyloxy)benzo [g]isoquinoline-5,10-dione respectively (8.85 g) .
m.p.. 156-158°C.
Preparative Example 11 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid and 4-(5-chloro-2-fluorobenzoyl)nicotinic acid Sec-butyllithium (1.3 M in cyclohexane; 6.0 mL) is added dropwise via a syringe to a stirred solution of 1-chloro-4-fluorobenzene (0.97 g) in THF (70 mL) at -75°C
which is kept under a nitrogen atmosphere. After stirring for additional 30 min, the yellow mixture is transferred dropwise via a jacketed canula into a stirred mixture of pyridine-3,4-dicarboxylic acid anhydride (1.00 g) in THF
(100 mL) at -78°C under a nitrogen blanket. The pale yellow solution is allowed to warm to -20°C for 4 hours.
The THF is removed at reduced pressure. The yellow solid obtained is dissolved in water (10 mL), cooled to 0°C, and acidified with dilute HC1 in an ice-bath and the resulting precipitate is collected by filtration. Upon heating the white solid with acetone (30 mL), an insoluble material remains (0.095 g), which by ~H-NMR analysis is a 94/4 mixture of 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid and 4-(5-chloro-2-fluorobenzoyl)nicotinic acid, respectively.
m.p.. 289-291°C.
After centrifugation, the supernate is removed and roto-evaporated to give crystals of a 94/6 mixture (by ~H-NMR analysis) of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid respectively (0.947 g).
m.p.. 236-237°C.
Sublimation of this mixture (0.025 g) at 180 205°C/0.5 mm Hg gives a white solid with a 98/2 ratio of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5 chloro-2-fluorobenzoyl)isonicotinic acid respectively (20 mg) .
4-(5-chloro-2-fluorobenzoyl)nicotinic acid: 'H
NMR (CDC13/CD30D 9/1) : 6.96 (m, 1H) ; 7.21 (d, 1N) ; 7.45 (m, 1H); 7.86 (m, 1H); 8.76 (d, 1H); 9.18 (s, 1H).
3-(5-chloro-2-fluorobenzoyl)isonicotinic acid:
'H-NMR (DMSO-d6) : 7. 37 (m, 1H) ; 7.75 (m, 2H) ; 7. 83 (d, 1H) ;
8.77 (s, 1H); 8.90 (d, 1H).
Preparative Example 12 4-(5-chloro-2-fluorobenzyl)nicotinic acid Zinc-copper couple (0.75 g) is added to a stirred mixture of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid of Preparative Example 11 (94/6 on a molar base; 0.60 g) in 75% formic acid. The exothermic and effervescent reaction mixture is stirred for 15 min before heating to 80°C for 2 hours. After cooling to 40°C, the mixture is filtered through a sintered glass funnel. The solid is washed with 75% formic acid (1 x 5 mL) and ethyl acetate (2 x 5 mL).
The mixture is concentrated by roto-evaporation to about 2 mL. The orange oil obtained is dissolved in 0.5 N HCl (3 mL) and extracted with ethyl acetate (3 x 10 mL), then saturated with NaCl and extracted with ethyl acetate/1,2-dimethoxyethane (2 x 5 mL). The combined extracts are dried with Na2S04 and the solvents removed by roto-evaporation to yield a yellow foam. The foam (0.541 g) is recrystallized in hot acetonitrile (1 mL) to yield 4-(5-chloro-2-fluorobenzyl)nicotinic acid (0.142 g).
m.p.. 174-176°C.
~H-NMR (CDC13/CD30D 9/1): 4.43 (s, 2H); 6.79 (m, 1H); 6.86 (m, 1H); 6.95 (m, 1H); 7.11 (d, 1H); 8.55 (d, 1H); 9.12 (s, 1H).
Preparative Example 13 9-chloro-6-fluorobenzo[g]isoquinoline-5,10-dione Fuming sulfuric acid (30% S03; 0.31 mL) is added to 4-(5-chloro-2-fluorobenzyl)nicotinic acid of Preparative Example 12. The dark mixture is heated quickly to 130°C for 10 min in a flask fitted with a cotton filled drying tube. After cooling to room temperature, the reaction mixture is quenched with ice (3 g) and extracted with methylene chloride (4 x 7 mL).
The combined extracts are dried with Na2S0~ and the solvent is removed by roto-evaporation to yield 9-chloro-6-fluoro-benzo[g]isoquinoline-5,10-dione as a yellow solid (0.045 g; 82% yield).
m.p.. 204-206°C.
~H-NMR (CDC13): 7.45 (m, 1H); 7.83 (m, 1H); 7.98 (d, 1H);
9.08 (d, 1H) ; 9.49 (s, 1H) .
Example 1 5-(p-toluenesulfonyloxy)-2-methylisoquino[8,7,6-cdJindazole-6(2H)-one The 1:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy) benzo[g] isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]isoquinoline-5,10-dione, of Preparative Example 10a, (0.041 g) is dissolved in dry pyridine ( 2 mL) and a freshly prepared 1M
solution of N-methyhydrazine in pyridine (0.183 mL) is added. After stirring for three hours at room temperature the reaction mixture is concentrated to dryness and added with water (5 mL), with NaH2P04 saturated solution (5 mL) and extracted several times with methylene chloride (50 mL). The combined organic solutions are dried ever anhydrous sodium sulfate and the solvent is removed at reduced pressure. The obtained residue is purified by silica-gel column chromatography (eluant: methylene chloride/ethyl acetate 90/10 v/v (50 mL), then 75/25 (50 mL), then 60/40 (50 mL) and finally 40/60 (50 mL) to give2-methyl-5-(p-toluenesulfonyloxy)isoquino[8,7,6-cd]
indazole-6(2H)-one.
~H-NMR (CDC13): 2.42 (s, 3H); 4.25 (s, 3H); 7.33 (d, 2H);
7.53 (d, 1H); 7.63 (d, 1H); 7.95 (d, 2H); 8.07 (d, 1H) 8.80 (d, 1H); 9.50 (s, 1H).
Example 2 2-[2-(dimethylamino)ethyl)]-5-(p-toluenesulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-one Under a nitrogen atmosphere a solution of 2-(dimethylaminoethyl)hydrazine (J. Med. Chem. 7, 493, 1964) (1.86 g) in anhydrous THF (6.0 mL) is added during 30' to the stirred 9:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (2.4 g) in THF (24 mL) containing N,N-diisopropylethylamine (1.10 mL). A
slightly exothermic reaction ensues, and the reaction temperature increases from 20°C to 25°C. After one hour at room temperature the reaction mixture is poured in water (240 mL) and the suspension obtained is stirred for 30' . The solid is separated by suction, washed with water and dried at 40°C to give 2-[2-(dimethylamino)ethyl)]-5 (p-toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6(2H)-one (1.44 g).
m.p.. 139-141°C.
'H-NMR (CDC13): 2.35 (s, 6H); 2.45 (s, 3H); 2.95 (t, 2H);
4.65 (t, 2H); 7.35 (d, 2H); 7.52 (d, 1H); 7.80 (d, 1H);
7.95 (d, 2H); 8.10 (d, 1H); 8.80 (d, 1H); 9.55 (s, 1H).
2143$53 Example 3 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluene-sulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-one (2-N-tert-butoxycarbonylaminoethyl)hydrazineis 5 prepared by reaction of N-t-butoxycarbonyl-2-chloro-ethylamine with hydrazine following a procedure adapted from J. Med. Chem. 7, 493, (1964). Under a nitrogen r atmosphere a solution of (2-N-tert-butoxycarbonyl aminoethyl)hydrazine (9.2 g) in anhydrous THF (10 mL) is 10 added during 30' to the stirred 9:1 mixture of 9-fluoro-6 (p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneand 9-chloro-6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (3.0 g) in THF (25 mL) containing N,N-diisopropylethylamine (1.38 mL). A
15 slightly exothermic reaction ensues, and the reaction temperature increases from 21°C to 24°C. After stirring for one hour at room temperature the obtained precipitate is recovered by suction, washed with THF/n-hexane 1/1 (15 mL) and dried at 40°C under vacuum, to give 2-[2-(N-tert-2o butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one (1.33 g).
m.p.. 206-208°C.
~H-NMR (CDC13) : 1.4 (s, 9H) ; 2.45 (s, 3H) ; 3.75 (q, 2H) ;
4.70 (t, 2H); 4.92 (br, 1H); 7.35 (d, 2H); 7.50 (d, 1H);
25 7.75 (d, 1N); 7.95 (d, 2H); 8.09 (d, 1H); 8.78 (d, 1H);
9.50 (s, 1H).
Example 4 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluene-sulfonyloxy) isoquino[8,7,6-c]indazole-6(2H)-one 30 A solution of 2-[(2-hydroxyethylamino)ethyl]-hydrazine (J. Het. Chem., 26, 85, (1989); 0.179 g) in absolute ethanol (0.5 mL) is dropped into a stirred solution of the 9:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-~143~~3 6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (0.200 g) in THF (2.0 mL) containing triethylamine (0.073 mL). After stirring for 2 hours at room temperature an additional amount of 2- [ ( 2-hydroxyethylamino)ethyl]hydrazine (0.179 g) in absolute ethanol (0.5 mL) is added and after two additional hours the reaction mixture is concentrated to the volume of about 1 mL. Water (20 mL) is added and the mixture is allowed to stir at room temperature overnight. The l0 precipitate is collected by suction filtration, dried under vacuum at 40°C and finally sludged in boiling ethyl acetate to give 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluenesulfonyloxy)isoquino[8,7,6-c]indazole-6(2H)-one (0.060 g).
m.p.. 131-133°C.
~H-NMR (DMSO-db/D20) : 2. 45 (s, 3H) ; 2 . 62 (t, 2H) ; 3. 13 (t, 2H); 3.40 (t, 2H); 4.65 (t, 2H); 7.25 (d, 1H); 7.40 (d, 2H); 7.75 (d, 2H); 7.95 (d, 1H); 8.15 (d, 1H); 8.80 (d, 1H); 9.40 (s, 1H).
Example 5 Preparation of 2-(aminoalkyl)-5-(p-toluenesulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-ones Using the procedure of Examples 1-4, the following compounds are obtained by reaction of the mixtures of 9-fluoro-6-(p-toluenesulfonyloxy) benzo[g]
isoquinoline-5,10-dione and 9-chloro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione of Preparative Example 10, with a substituted hydrazine selected from the group of 2-(diethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 3-dimethylaminopropylhydrazine [J. Het.
Chem., 23, 1491, (1986)], 2-aminoethylhydrazine [J. Het.
Chem., 23, 1491, (1986)], 2-(methylaminoethyl)hydrazine, 2-hydroxyethylhydrazine, 3-aminopropylhydrazine [J. Het.
Chem., 23, 1491, (1986)];
2-[2-(diethylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one;
2-[3-(dimethylamino)propyl]-5-(p-toluenesulfonyloxy)iso-q a i n o [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[2-(amino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[2-(methylamino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[3-(amino)propyl]-5-(p-toluenesulfonyloxy)isoquino [8,'7,6-cd]indazole-6(2H)-one.
Example 6 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one A solution of methyl hydrazine (0.76 M; 0.021 g) in pyridine (0.6 mL) is added dropwise over two min to a stirred solution of9-chloro-6-fluorobenzo[g]isoquinoline-5,10-dione of Preparative Example 13 in pyridine (0.5 mL) cooled with an ice-bath. A yellow precipitate appears in the dark solution after 6 min. After 1.3 h the reaction mixture is reduced to half its volume by a gentle stream of nitrogen and quenched with ice (5 g). The pale yellow precipitate is collected by suction filtration and washed with ice-water (2 x 1 mL) and dried under vacuum. The yellow solid is purified by silica gel column chromatography (eluant: chloroform/methanol 96/4 v/v) to yield 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.033 g; 71% yield) as a yellow solid.
m.p.. 244-245°C.
~H-NMR (CDC13): 4.25 (s, 3H); 7.59 (dd, 2H); 7.92 (d, 1H);
8.84 (d, 1H); 9.55 (s, 1H).
Example 7 Preparation of 2-(aminoalkyl)-5-chloroisoquino[5,6,7-cd]indazole-6(2H)ones Using the procedure of Example 6 the fdllowing compounds are obtained by reaction of 9-chloro-6-fluorobenzo[g]isoquinoline-5,1o-dione of Preparative Example 13 with a substituted hydrazine selected from the r _~~43853 group of (2-N-tert-butoxycarbonylaminoethyl) hydrazine, 2- -(dimethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 2- -(diethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 2-[(2-hydroxyethylamino)ethyl]hydrazine (J.
Het. Chem., 26, 85, (1989)], 3-dimethylaminopropyl-hydrazine [J. Het. Chem., 23, 1491, (1986)], 2-amino-ethylhydrazine [J. Het. Chem., 23, 1491, (1986)], 2-(methylaminoethyl)hydrazine, 2-hydroxyethylhydrazine, 3- -aminopropylhydrazine [J. Het. Chem., 23, 1491, (1986)];
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-chloroisoquino [5,6,7-cd]indazole-6(2 H)-one;
m.p.. 226-228°C.
~H-NMR (CDC13 + CD~OD) : 1. 30 (s, 9H) ; 3.58 (t, 2H) ; 4.63 (t, 2H); 7.54 (d, 1H); 7.70 (d, 1H); 7.90 (dd, 1H); 8.70 (d, 1H); 9.40 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
m.p.. 160-161°C.
~H-NMR (CDC13): 2.32 (s, 6H); 2.95 (t, 2H); 4.65 (t, 2H);
7.60 (d, 1H); 7.69 (d, 1H); 8.00 (dd, 1H); 8.88 (d, 1H);
9.60 (s, iH);
2-[2-(diethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(diethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one;
m.p.. 148-152.5°C.
~H-NMR (CDC13 + CD30D) : 2.75 (t, 2H) ; 3. 43 (t, 2H) ; 3. 60 (t, 2H) ; 4. 63 (t, 2H) 7. 55 (d, 1N) ; 7 .75 (d, 1H) ; 7.98 (dd, 1H); 8.73 (d, iH); 9.40 (s, 1H);
2-[3-(dimethylamino)propyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(amino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
2-[2-(methylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(hydroxy)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
2-[3-(amino)propyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
Example 8 5-[[2-(dimethylamino)ethyl]amino)-2-methylisoquino[8,7,6-cd]indazole-6(2H)-one A 1M solution of N,N-dimethylethylenediamine in pyridine (0.10 mL) is added to a stirred suspension of 2-l0 methyl-5- (p-toluenesulfonyloxy)isoquino [8,7,6-cd]
indazole-6(2H)-one (0.02 g) in dry pyridine (2 mL). After stirring at room temperature for one hour the reaction mixture is heated at 70°C for 13 hours while additional amounts of N,N-dimethylethylenediamine solution (0.1;
0.05; 0.05 mL) are added after 2, 4 and 11 hours respectively. Pyridine and excess N,N-dimethylethyl-enediamine are removed by distillation at reduced pressure and the obtained residue is partitioned between CH2C12 (50 mL) and brine (10 mL) to which NaHC03 saturated solution is added (1 mL). The organic solution is dried over anhydrous Na2S04 and the solvent removed by distillation.
The orange residue obtained is purified by silica-gel column chromatography (eluant: CHC13/MeOH 95/5 (30 mL) followed by CHC13/MeOH/NH,~OH 90/15/0.5 (50 mL) to give 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino [8,7,6-cd] indazole-6(2H)-one (0.011 g) as a reddish orange solid.
m.p.. 208-215°C (dec.).
'H-NMR (CDC13): 2.40 (s, 3H); 2.75 (t, 2H); 3.57 (q, 2H);
4. 25 (s, 3N) ; 6.97 (d, 1H) ; 7. 63 (d, 1N) ; 8. 30 (dd, 1H) 8.79 (d, 1H) ; 9.30 (br.t, 1H) ; 9.62 (d, iH) .
_2143853 Example 9 2-[2-(dimethylamino)ethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[8,7,6-cd]indazole-6(2N)-one A solution of 2-[2-(dimethylamino)ethyl]-5-(p-5 toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6 (2H)-one of Example 2 (0.463 g) and 2-(dimethylamino)ethylamine (0.80 mL) in dry pyridine (4.63 mL) is heated at 80°C for 1 h, 30~ under a nitrogen blanket. The solution is then concentrated to dryness and the dark residue obtained is 10 partitioned between brine (30 mL) and ethyl acetate (4 x 25 mL). The combined organic solutions are dried over Na2S04 and concentrated to about 3 mL. After addition of n-hexane (12 mL) and stirring for one hour the precipitate is collected by suction and dried at 40°C
15 under vacuum to give 2-[2-(dimethylamino)ethyl)]5-[[2-(dimethylamino) ethyl]amino] isoquino[8-,7,6-cd]indazole-6(2H)-one (0.23 g).
m.p.. 150-152°C.
~H-NMR (CDC13): 2.32 (s, 6 H); 2.40 (s, 6H); 2.70 (t, 2H);
20 2 . 95 (t, 2H) ; 3 . 60 (q, 2H) ; 4 . 65 (t, 2H) ; 6. 98 (d, 1H) ;
7.70 (d, 1H); 8.30 (d, iH); 8.80 (d, 1H); 9.30 (br, 1H);
9.65 (s, 1H).
Example 10 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(N-tert-25 butoxycarbonylamino)ethyl]amino]isoquino[8,7,6-cd]
indazole-6(2H)-one A suspension of 2-[2-(N-tert-butoxycarbonyl-amino)ethyl]-5-(p-toluenesulfonyloxy)isoquino(8,7,6-cd]
indazole-6(2H)-one of Example 3 (0.535 g) and N-(tert-30 butoxycarbonyl)ethylenediamine (prepared according to Synt. Comm., 20, 2559, (1990); 1.12 g) in dry pyridine (5.35 mL) is heated at 80°C. The dark solution obtained is held at this temperature for 5 hours, then it is concentrated to dryness and partitioned between brine (30 35 mL) and ethyl acetate (2 x 25 mL). The orange-red solid insoluble in the biphasic mixture is separated by suction filtration and dried at 40°C under vacuum (0.43 g).
This material (0.60 g) is purified by column chromatography (Si02; eluant methylene chloride/methanol from 90/10 to 70/30 v/v). The fractions containing the product are pooled and concentrated to about 20 mL and 2 [2-(N-tert-butoxy carbonylamino)ethyl]-5-[[2-(N-tert butoxycarbonylamino) ethyl]amino]isoquino[8,7,6-cd]
indazole-6(2H)-one separates as red-orange crystals (0.45 g).
m.p.. 211-213°C.
~H-NMR (CDC13/DMSO-db 9/1): 1.3 (s, 9H); 1.4 (s, 9H); 3.32 (q, 2H); 3.58 (m, 4Hj; 4.58 (t, 2H); 6.20 (br, 1H); 6.4a (br, 1H); 7.05 (d, 1H); 7.70 (d, 1H); 8.15 (d, 1H); 8.65 (d, 1H); 9.20 (br, 1H); 9.49 (s, 1H).
Example 11 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[(2-(dimethyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one A suspension of 2-[2-(N-tert-butoxycarbonyl-aminojethyl]-5-(p-toluenesulfonyloxy) isoquino[8,7,6- cd]
indazole-6(2H)-one (0.056 g) and 2-(dimethylamino) ethylamine (0.080 mL) in dry pyridine (0.50 mL) is heated at 80°C. The dark solution obtained is held at this temperature for 1 hour, then it is left at room temperature overnight. The dark precipitate obtained is separated by suction and purified by column chromatography (Si02; eluant ethyl acetate and then methylene chloride/methanol 9/0.5 v/v) to give 2-[2-(N-tert-butoxy-carbonylamino)ethyl)-5-[[2-(dimethylamino) ethyl) amino]
isoquino[8,7,6-cd]indazole-6(2H)-one (0.024 g) as a red-orange solid.
m.p.. 225-227°C (from methylene chloride).
~H-NMR (CDC13) : 1.43 (s, 9H) ; 2.40 (s, 6H) ; 2.7 (t, 2H) ;
3.55 (q, 2H); 3.78 (m, 2H); 4.65 (t, 2H); 5.23 (br.m, 1H);
6.87 (d, 1H); 7.62 (d, 1H); 8.28 (dd, 1H); 8.76 (d, 1H);
9.6 (s, 1H).
_2143853 Example 12 isoquino[8,7,6-cd]indazole-6(2H)-ones Following the procedures of Examples 8-11, the following compounds are prepared by reaction of 2-[2-(dimethylamino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6 (2H)-one of Example 2, 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6 -cd]indazole-6(2H)-one of Example 3, or 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluenesulfonyloxy) isoquino[8,7,6-c] indazole-6(2H)-one of Example 4 with the properly selected amine:
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxy-ethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 3.25 (m, 6H); 3.61 (t, 4H); 3.71 (m, 4H);
3.98 (q, 2H); 4.65 (t, 2H); 5.31 (br, 2H); 7.08(d, 1H), 7.70 (d, 1H); 8.30 (d, 1H); 8.83 (d, 1H); 9.30 (br, 1H);
9.69 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[3-(amino)propyl]a mino] isoquino[8,7, 6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.05 (m, 2H); 3.18 (m, 4H); 3.58 (t, 2H);
3.65 (t, 2H); 3.78 (q, 2H); 4.62 (t, 2H); 5.20 (br, 3H), 7.10 (d, 1H); 7.69 (d, 1H); 8.30 (d, 1H); 8.85 (d, 1H);
9.15 (br, 1H); 9.30 (t, 1H); 9.71 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[8,7, 6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 3.20 (m, 4H), 3.58 (t, 2H); 3.66 (t, 2H);
3.86 (q, 2H); 4.61 (t, 2H); 5.15 (br, 3H); 7.12(d, 1H);
7.69 (d, 1H); 8.30 (d, 1H); 8.85 (d, 1H); 9.15 (br, 1H);
9.30 (t, 1H); 9.71 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquin o[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.61 (s, 3H); 3.06 (t, 2H); 3.20 (t, 2H);
3.58 (t, 2H); 3.67 (t, 2H); 3.88 (q, 2H); 4.65 (t, 2H);
5. 10 (t, 1H) ; 7 (d, 1H) ; 7 .70 (d, 1H) ; (d, 1H) . 05 8. 33 ;
8.81 (d, 1H); 8.99 (br, 2H); 9.35 (t, 1H); 9.66(s, 1H).
2-[2-[(2-hydroxyethylamino]ethyl]-5-[[2-(dimethylamino) ethyl] amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.42 (s, 6H); 2.75 (t, 2H); 3.18 (t, 2H);
3.58 (q, 2H); 3.63 (t, 2H); 3.68 (t, 2H); 4.61 (t, 2H);
5. 15 (t, 1H) ; 6.99 (d, 1H) ; 7 . 66 (d, 1H) ; 8. 31 (d, 1H) ;
8.80 (d, 1H); 9.11 (br, 1H); 9.35 (t, 1H), 9.65 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(N-tert-butoxy-carbonylamino)ethyl]amino]isoquino[8,7,6-cd] indazole-6 (2H)-one;
'H-NMR (CDC13 + CD30D) : 1.40 (s, 9H) ; 3: 31 (m, 4H) ; 3.52 (q, 2H); 3.63 (t, 2H); 3.85 (t, 2H); 4.71 (t, 2H); 7.03 (d, 1H); 7.70 (d, 1H); 8.21 (dd, 1H); 8.76 (d, 1H); 9.61 (s, 1H) .
2-[2-(N-tert-butoxycarbonylamino)ethy)]-5-[[2-[(2 hydroxyethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole 6(2H)-one 'H-NMR (CDC13 + CD30D) : 1.45 (s, 9H) ; 3. 18 (m, 4H) ; 3 .73 (q, 2H); 3.80 (m, 4H); 4.67 (t, 2H); 7.00 (d, 1H); 7.68 (d, 1H); 8.25 (dd, 1H); 8.75 (d, 1H); 9.60 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
m.p.. 156-157°C.
'H-NMR (CDC13): 2.30 (s, 6H); 2.91 (m, 4H); 3.08 (t, 2H);
3.60 (t, 2H); 3.75 (m, 2H); 4.60 (t, 2H); 6.90 (d, 1H);
7.60 (d, 1H); 8.25 (dd, 1H); 8.75 (d, 1H); 9.45 (br, 1H);
9.60 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2. 30 (s, 6H) ; 2.95 (t, 2H) ; 3. 13 (t, 2H); 3.65 (t, 2H); 4.58 (t, 2H); 7.04 (d, 1H); 7.70 (d, 1H); 8.18 (dd, iH); 8.66 (d, 1H); 9.51 (s, 1H).
. _ 2143853 Example 13 5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6 (2H)-one of Example 6 (0.013 g) is added to 2-(dimethyl-amino)ethylamine (0.34 mL). The yellow mixture is heated quickly to reflux for 1 hour. The excess diamine is removed from the orange solution by a gentle stream of nitrogen. The orange mixture obtained is purified by l0 silica gel column chromatography with a gradient elution (1% methanol/chloroform (25 mL), 2% methanol/chloroform (25 mL), 4% methanol/chloroform (25 mL), 8%
methanol/chloroform (25 mL), 12% methanol/chloroform (25 mL), 16% methanol/chloroform (25 mL), 24%
methanol/chloroform (50 mL)) to yield 5-[[2-(dimethyl-amino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.010 g) as a reddish orange solid.
m.p.. 212-216°C.
~H-NMR (CDC13): 2.36 (s, 6EI); 2.69 (t, 2H); 3.54 (q, 2H);
4.21(s, 3H); 6.91 (d, 1H); 7.54 (d, lH); 8.00 (d, 1H);
8.79 (d, 1H); 9.19 (br, 1H); 9.67 (s, 1H).
Example 14 2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[5,6,7-cd]indazole-6(2H)-one Under a nitrogen atmosphere N,N-dimethylethylenediamine (1.79 mL) is added to a stirred solution of 2-[2-(dimethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one (0.539 g) in pyridine (6.80 mL) and the resulting solution is heated at 80°C for 12 hours. The pyridine and excess N,N-dimethylethylenediamine are removed by roto-evaporation and the obtained residue is purified by silica gel column chromatography eluting first with methylene chloride, then with methylene chloride/methanol 95/5 and finally with methylene chloride/methanol/concd. ammonia from 95/5/0.5 to 95/5/1 v/v/v. The fractions containing the yellow desired product are pooled and the solvents roto-evaporated. The obtained residue (0.529 g) is crystallized from 5 diisopropylether to give 2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one as a yellow powder (0.291 g).
m.p.. 110-111°C.
'H-NMR (CDC13): 2.31 (s, 6 H); 2.38 (s, 6H); 2.71 (t, 2H);
10 2.92 (t, 2H); 3.55 (q, 2H); 4.65 (t, 2H); 7.01 (d, 1H);
7.69 (d, 1H); 8.10 (dd, 1H); 8.83 (d, 1H); 9.30 (br.t., 1H) ; 9.71 (s, 1H) .
Example 15 15 isoquino[5,6,7-cd]indazole-6(2H)-ones Using the procedures of Example 13 or 14, the following compounds are prepared by reaction of 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one, 2-[2-(dimethylamino)ethyl)-5-20 chloroisoquino[5,6,7-cd]indazole-6(2H)-one, or 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one of Example 7:
2-[2-(N-tert-butoxycarbonylamino)ethyl)-5-[[2-(N-tert-butoxycarbonylamino)ethyl]amino] isoquino[5,6,7-25 cd]indazole-6(2H)-one;
m.p.. 211-213°C.
'H-NMR (CDC13): 1.40 (s, 9H); 1.46 (s, 9H); 3.55 (q, 2H);
3.65 (q, 2H); 3.77 (q, 2H); 4.69 (t, 2H); 5.55 (br, 2H);
7.00 (d, 1H); 7.60 (d, 1H); 7.93 (dd, 1H); 8.70 (d, 1H);
30 9.10 (br.t., 1H); 9.38 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(amino)ethyl)amino)isoquino[5,6,7-cd]indazole-6(2H)-one;
(reaction performed at 50°C in DMSO as the solvent) m.p.. 221-222°C.
35 ~H-NMR (CDC13): 1.43 (s, 9H); 3.13 (t, 2H); 3.58 (q, 2H);
3.75 (q, 2H); 3.67 (t, 2H); 5.05 (br, 1H); 7.00 (d, 1H);
. 2143853 7.65 (d, 1H); 8.05 (dd, 1H); 8.60 (d, 1H); 9.30 (br., 1H);
9.75 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-[[2-[(2 hydroxyethyl)amino]ethyl]ami no]isoquino[5,6,7 cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 1.48 (s, 9H) ; 3.25 (m, 4H) ; 3.74 (q, 2H); 3.80 (m, 4H); 4.68 (t, 2H); 7.01 (d, 1H); 7.72 (d, 1H); 8.09 (dd, 1H); 8.80 (d, 1H); 9.75 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-[[2-(dimethyl-l0 amino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13): 1.44 (s, 9H); 2.31 (s, 6H); 2.75 (t, 2H);
3.68 (q, 2H); 3.75 (q, 2H); 4.68 (t, 2H); 5.10 (br.m.,H);
7.03 (d, 1H); 7.70 (d, 1H); 8.15 (dd, 1H); 8.85 (d, 1H);
9.33 (br.t., 1H); 9.71 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D) : 2. 40 (s, 6H) ; 2.95 (t, 2H) ; 3 . 23 (m, 4H); 3.82 (m, 4H); 4.70 (t, 2H); 7.05 (d, 1H); 7.70 (d, 1H); 8.13 (dd, 1H); 8.85 (d, 1H); 9.70 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]iso-quino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13): 2.39 (s, 6H); 2.95 (t, 2H); 3.15 (t, 2H);
3.68 (q, 2H); 4.68 (t, 2H); 7.00 (d, 1H); 7.65 (d, 1H);
8.12 (dd, 1H); 8.85 (d, 1H); 9.33 (br.t., 1H); 9.72 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxyethyl) amino] ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(reaction performed at 52°C in DMSO as solvent) m.p.. 148-151°C.
~H-NMR (D20): 2.75 (m, 6H); 2.95 (m, 2H); 3.12 (m, 2H);
3.70 (m, 4H) ; 4.05 (m, 2H) ; 6. 10 (d, 1H) ; 6. 65 (d, 1H) ;
6.90 (d, 1H); 7.83 (s, 1H); 7.95 (d, 1H).
2143$53 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2 . 97 (t, 2H) ; 3. 30 (m, 4H) ; 3 . 68 (t, 2H); 3.85 (t, 2H); 4.66 (t, 2H); 7.00 (d, 1H); 7.69 (d, 1H); 8.10 (dd, 1H); 8.83 (d, 1H); 9.76 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[3-(amino)propyl]amino] isoquino[5,6,7-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2. 09 (m, 2H) ; 2. 57 (t, 2H) ; 3. 30 (m, 4H); 3.53 (t, 2H); 3.82 (t, 2H); 4.66 (t, 2H); 7.01 (d, 1H); 7.68 (d, 1H); 8.05 (dd, 1H); 8.80 (d, 1H); 9.68 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl] amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D) : 2.48 (s, 3H) ; 2.83 (t, 2H) ; 3.28 (m, 4H); 3.58 (t, 2H); 3.83 (t, 2H); 4.67 (t, 2H); 7.01 (d, 1H); 7.68 (d, 1H); 8.03 (dd, 1H); 8.80 (d, 1H); 9.67 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethyamino) ethyl] amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D): 2.31(s, 6H); 2.72 (t, 2H); 3.33 (m, 4H) ; 3. 57 (t, 2H) ; 3 . 87 (t, 2H) ; 4 . 71 (t, 2H) ; 7. 00 (d, 1H); 7.71 (d, 1H); 8.09 (dd, 1H); 8.81 (d, 1H); 9.70 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(N-tert-butoxy carbonylamino)ethyl]amino]isoquino[5,6,7-cd]indazole-6 (2H)-one;
'H-NMR (CDC13 + CD30D) : 1.41 (s, 9H) ; 3. 29 (m, 4H) ; 3.56 (t, 2H); 3.79 (t, 2H); 3.83 (t, 2H); 4.68 (t, 2H); 7.05 (d, 1H); 7.68 (d, 1H); 8.08 (dd, 1H); 8.80 (d, 1H); 9.68 (s, 1H).
Example 16 Removal of the t-butoxycarbonyl protective group Under a nitrogen atmosphere an ethanolic solution of anhydrous HC1 (5N; 0.40 mL) is dropped into a stirred suspension of 2-[2-(N-tert-butoxycarbonylamino) ethyl]-5-[[2-(N-tert-butoxycarbonylamino) ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one of Example 10 (0.104 g) in absolute ethanol (2.1 mL). Initial dissolution of the starting material followed by precipitation of a dark-red solid is observed during the addition of ethanolic HC1. This solid is redissolved with absolute ethanol and the solution is heated to 40°C for 2 h, 30'. The gradual formation of a red-amaranth precipitate is observed during the heating. After cooling to room temperature diethyl ether ( l0 mL) is added and the precipitate is collected by suction filtration under a nitrogen blanket, to give 2-[2-(amino)ethyl]-5-[[2-(amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one trihydrochloride (0.070 g).
m.p.. 247-250°C.
~H-NMR (D20) : 3.40 (t, 2H) ; 3.70 (t, 2H) ; 3 . 95 (t, 2H) ;
4.87 (t, 2H); 7.05 (d, 1H); 7.78 (d, 1H); 8.04 (dd, 1H);
8.62 (d, 1H); 9.10 (s, 2H).
UV (HZO) : ~",ex (E~~) = 230 nm (650 cm) ; 240 nm (555 cm) ; 370 nm (244 cm); 591 nm (342 cm).
Example 17 Following the procedure of Example 16, the following compounds are prepared as the trihydrochloride salt starting from the appropriate N-tent-butoxycarbonyl derivatives of Examples 11, 12, 14, or 15:
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
~H-NMR (D20) : 3. 07 (t, 2H) ; 3 . 39 (m, 4H) ; 3 . 69 (t, 2H) ;
3.88 (t, 2H) ; 4.83 (t, 2H) ; 7. 05 (d, 1H) ; 7.70 (d, 1H) ;
8.33 (dd, 1H); 8.78 (d, 1H); 9.15 (s, 1H).
,, ,. ~ 2143853 2-[2-(amino)ethyl)]-5-[[2-[(2-hydroxyethyl)amino]ethyl]
aminoJisoquino[8,7,6-cd]indazole-6(2H)-one;
~H-NMR (DZO): 3.28 (t, 2H); 3.31 (m, 4H); 3.85 (m, 4H);
4.90 (t, 2H); 7.03 (d, 1H); 7.70 (d, 1H); 8.35 (dd, 1H);
8.72 (d, 1H); 9.77 (s, 1H).
2-[2-(amino)ethyl)]-5-[[(2-(dimethylamino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one m.p.. 224C (dec.).
'H-NMR (Dz0): 3.00 (s, 6H); 3.60 (t, 2H); 3.70 (t, 2H);
4.07 (t, 2H); 4.93 (t, 2H); 7.20 (d, 1H); 7.95 (d, 1H);
8.43 (dd, 1H); 8.77 (d, 1H); 9.43 (s, 1H).
UV (HC1 0. 1N) : ~~,ax (E~~) - 236 nm (485 ; 382 nm (205 cm) cm); 507 nm (232 cm).
2-[2-(amino)ethyl]-5-[[2[(amino)ethyl]aminoJ isoquino [5,6,7-cd]indazole-6(2H)-one m.p.. > 260C.
~H-NMR (D20) : 3 . 42 (t, 2H) ; 3.75 (t, 2H) 4.00 (t, 2H) ; ;
5.05 (t, 2H); 7.32 (d, 1H); 8.09 (d, 1H); 8.62 (d, 1H);
8.87 (d, 1H); 9.55 (s, 1H) UV (HC1 0. 1N) : ~",ax (E~~) - 245 nm (622 cm) 275 nm ;
(181 cm); 351 nm (258 cm); 472 nm (327 cm), 494 nm (353 cm).
2-[2-(amino)ethyl)]-5-[[-[(2-hydroxyethyl)amino]ethyl]
amino] isoquino[5,6,7-cd]indazole-6(2H)-one;
2-[2-(amino)ethyl)]-5-[[2-(dimethylamino)ethyl]amino]
isoquino[5,6,7-cd]indazole -6(2H)-one;
Example 18 2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate A solution of malefic acid (0.030 g) in absolute ethanol (0.4 mL) is added drop-wise into a stirred solution of 2-[2-(dimethylamino) ethyl]-5-[[2-(amino) ethylJamino]isoquino[8,7,6-cd]indazole-6(2H)-one of Example 12 (0.030 g) in absolute ethanol (1.5 ml) held at ._ 50°C. After the addition is complete the reaction mixture is maintained at 50°C for 3 minutes and then allowed to cool to room temperature. After one hour the red-amaranth crystalline material which separated is filtered, washed 5 with ethanol and dried under vacuum at 40°C to give 2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]isoquino [8,7,6-cd]indazole -6(2H)-one dimaleate (0.029 g).
m.p.. 175-175.5°C.
~H-NMR (DZO): 3.00 (s, 6 H); 3.40 (t, 2H); 3.80 (t, 2H);
10 3.93 (t, 2H); 4.90 (t, 2H); 6.00 (s, 4H); 7.00 (d, 1H);
7.70 (d, 1H); 7.80 (d, iH); 8.55 (d, 1H); 9.00 (s, 1H).
UV (HC1 0. 1N) : ~",ax (E~~) - 236 nm (436 cm) ; 382 nm (169 cm); 507 nm (190 cm).
Example 19 15 Following the procedure of Example 18, the following maleate salts are prepared by salification of the appropriate isoquinoindazole-6(2H)-ones with malefic acid:
2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino] isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate 20 m.p.. 189-191C.
~H-NMR (DMSO-db): 2.88 (s, 12H); 3.37 (t, 3.70 2H);
(t, 2H); 3.95 (q, 2H); 5.01 (t, 2H); 6.00 (s, 4H); 7.38 (d, 1H); 8.20 (dd, 1H); 8.85 (d, 1H); 9.20 (br.t., 1H);
9.55 (s, 1H).
25 UV (HZO) : ~,",x (E,~)- 368 nm (154 cm) ; 469 nm (206 cm) ;
490 nm (211 cm).
2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino] isoquino[5,6,7-cd]indazole-6(2H)-one dimaleate m.p.. 142-146C.
30 ~H-NMR (D20) : 3.00 (s, 6H) ; 3.05(s, 6H) ; 3.60(t, 2H) ;
3.92 (t, 2H) ; 4. 08 (t, 2H) ; 5.07(t, 2H) ; 6. (s, 4H) 15 ;
7.20 (d, 1H); 7.95 (d, 1H); 8.20 (d, 1H); 8.75 (d, 1H);
9.30 (s, 1H).
UV (H20) : ~",ax (E~~) - 292 nm (108 cm) ; 352 nm (133 cm) ;
35 476 nm (215 cm) .
_2143853 2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate m.p.. 156-157°C.
~H-NMR (D20) : 3. 05 (s, 6H) ; 3 . 30 (m, 2H) ; 3 . 54 (t, 2H) ;
3.88 (m, 4H); 4.03 (t, 2H); 4.96 (t, 2H); 6.00 (s, 4H);
7.00 (d, 1H); 7.70 (d, 1H); 7.83 (dd, 1H); 8.57 (d, 1H);
9.05 (s, 1H) (HzD) ~ ~max (Em) - 368 nm (1057 cm) ; 491 nm (210 cm) .
NH-A
Yi \
i X
I I
N N~B
C
TABLE 1 (Continued) o. Y X R A B
1 CH N H C"HZCHZNHCHZCHZOH CHZCHZNHCHZCHZOH
2 CH N H CHZCH~CHZNHZ "' 3 CH N H CH~CH2NHz "' 4 CH N H C'HZCHZNHC:H3 "' 5 CH N H C"HZCH~N (CHI) Z "' 6 N CH H C'HzCH2NHC:HzCHZOH CHZCHZNHCHzCH20H
7 N CH H C'HZCH2CHpNII~ "' 8 N CH H t.'HzCH2NH~ ' 9 N CH H C~H~CH2NHCH3 ", 10 N CH H C~'HZCH~N (CH_i) Z "' 11 CH N H C"HZCHZNH('H~CHZOH CHZCHZN (CH3) ~;
12 CH N H C"H2CH~CH~NH2 "' 13 CH N H C'HZCHZNH~ "' 14 CH N H C'HZCHZNHC"H3 "' 15 CH N H CHZCHZN (C'H S ) ~ "' 16 N CH H C'HZCH ZNHCHZCH?OH CH 2CHZN (CH3) a 17 N CH H CHZCH2CHZNHz "' 18 N CH H C'H~CHZNH~ "
19 N CH H CHzCH2NH('H3 ' 20 N CH H t,HZCH~N (C"H,~) Z "' 21 CH N H C"HZCH~NHC'HzCHZOH CHZCHZNHZ
22 CH N H C~H~,CHZCH~N)-IZ "' 23 CH N H C~HZC~HZNH~
24 C~'H N H ('HZCH~NH(~H ~ "' 25 CH N H lv"HZCH~N (C'H.3) ? ' 26 CH N H C"HZt~'H~NIIC'H~CEi20HCHZCHZCHZNHZ
27 CH N H Cl-i2CH~N1-12 "' 29 CH N H C'H~CHZN11CH; "' 30 CH N H C:'H~C.'H~N (C'H,3) ' z 31 N CH H C'HzCH2NHCH~CH20H CHZCHZCHZNHZ
32 N CH H CVHzCH2NH(:'H-~CHZOH CH2CHZNH2 33 CH N H C"HZCH~NH(~H~CHZOH CHZCHZNHCH3 34 CH N H CH~CH~CH~NH~ ' 35 CH N H C'~IZCH~NH~ "
36 CH N H C'li2CH~NHC"H_{
37 CH N N (.'1-i2CH~N (C:H.~) "
Z
38 N CH H C~H~CHZNHCH;CHZOH CHZCHZNHCH3 39 N CH H CH~CH~CH-~f-IZ "
40 N CH H ('HZCH~NH~ "
41 N CH H C'HZCH~NHC'H~ "
42 N CH H C,I12C1-IzN (CHI) 2 "
43 CH N H C'HZCH~N (CH3) z CH3 44 N CH H C'H~CHZN (C~'H~) ~ CH3 The compounds of this invention can be prepared by the process depicted in scheme 1 and involving the reaction (reaction a) of a compound of formula {1II):
R O Z
X .,,' W
5 (IIIa) X = N, Y = C'.H
~( I IIb ) X = CH, Y = N
wherein Z is OTs (OTs being the p-toluenelsulfonyloxy group) or Cl and W is F or Cl, with the proviso that Z and W can not simultaneously be C1, with a hydrazine of formula { IV ):
10 HZN-NH-B' (IV) where B' has the sanue meanings as B is defined in fornmla (I), or B' is a group that can be converted into B by removal of protective groups for the primary or secondary amines aptionally present in B', to give a compound of formula (II):
R p . Z
Y.o W /
f Nw---N~B>
l Ila) X = N, Y = CH
{IIb) X-CH, Y=N
which then is reacted (reaction b) with a compound of formula (V):
HZN--A' ( V ) where A' has the same meanings as A is defined in formula (I), or A' is a group that can be converted into A by removal of protective groups for the primary or secondary amines optionally present in A', to give the compounds of formula (I'):
R O NH_A, y~ \
X\ I ~ ~ , (I ) N N~B, When A' and/or B' are different from A and/or B, compounds of formula (I') are converted to compounds of formula (I) by removal of the protective groups for the primary~and/or secondary amines optionally present in A' and/or B'.
When, if desired, the process depicted in scheme 1 is performed by reacting compounds of formula (IIIa), then the compounds of the invention of formula (Ia) can be obtained where X represents an atom of nitrogen and Y
represents a carbon atom. Alternatively, if desired, by 2o reacting compounds of formula (IIIb), the compounds of formula (Ib) can be obtained.
Protective groups for the primary and/or secondary amines optionally present in A' and/or B' which can advantageously be used for the preparation of compounds of formula (I) are represented by (C~-Cj) acyl-derivatives (preferably acetyl-derivatives), (C,-C4) alkoxycarbonyl-derivatives (preferably. tert-butoxy-carbonyl-derivatives) and by (C~-C,o)aralkyloxycarbonyl-derivatives (preferably benzyloxycarbonyl-derivatives).
w 2143853 In a preferred embodiment of this invention, compounds of formula (I) are prepared by reaction of a compound of formula (III'):
R O OTs Y
I (III') X
O
with a hydrazine of formula (IV) to give a compound of formula (II'):
R O OTs Y / I \ (II') X~ /
N N~B, Compounds of formula (II' ) are then reacted with a compound of formula (V) to give a compound of formula (I'), which step is followed by removal of the protective groups for the primary and secondary amines optionally present in A' and/or B', to give a compound of formula (I) .
In another preferred embodiment of this invention compounds of formula (I) wherein X is C and Y is N are preferably prepared by reaction of a compound of formula (III" ) R O F
(III" ) N\
_21~38~3 with a hydrazine of formula (IV) to give a compound of formula (II" ) I~ N-N'~
l N I I \ (II,.) /
p CI
Compounds of formula (II " ) are then reacted with a compound of formula (V) to give a compound of formula (I'), which step is followed by removal of the protective groups for the primary and secondary amines optionally present in A' and/or B', to give a compound of formula (I) wherein X is C and Y is N.
The reaction of compounds (III) with the hydrazines (IV) can be performed by heating compounds (III) with a stoichiometric amount of hydrazines (IV) or an excess of hydrazines (IV). The reaction is usually performed in an inert solvent such as methylene chloride, chloroform, 1,1,1-trichloroethane, dimethoxyethane, tetrahydrofuran, dimethylsulfoxide, dimethylformamide, pyridine, picoline, and mixtures thereof, or if it is desired, using compound (IV) itself as the solvent, optionally in the presence of an inorganic base such as an alkaline or alkaline-earth carbonate or hydrogen carbonate or an organic base such as a trialkylamine, at a temperature from 0°C to the reflux temperature of the solvent.
Preferably the reaction is carried out in a solvent such as pyridine, tetrahydrofuran, dimethyl-sulfoxide, or N,N,N',N'-tetramethylethylenediamine, using from 2 to l0 equivalents of compound (IV) for 1 equivalent of compound (III), and working at a temperature ranging from 5°C to 50°C.
_2143853 When, in a particular embodiment of this invention, a compound of formula (III') is reacted with a hydrazine of formula (IV), the reaction is preferably performed with a molar ratio between compounds (III) and (IV) of 1:1.05 to 1:1.25 and by using tetrahydrofuran as solvent at a temperature ranging from room temperature to 50°C.
The reaction of the compounds of formula (II) with the compounds of formula (V) can be performed by l0 heating compounds (II) with a stoichiometric amount of amine (V) or an excess of amine (V). The reaction is usually performed in an inert solvent such as methylene chloride, chloroform, 1,1,1-trichloroethane, dimethoxyethane, tetrahydrofuran, dimethylsulfoxide, dimethylformamide, pyridine, picoline, and mixtures thereof, or, if it is desired, using compound (V) itself as the solvent, optionally in the presence of an inorganic base such as an alkaline or alkaline-earth carbonate or hydrogen carbonate or an organic base such as a trialkylamine, at a temperature from 0°C to the reflux temperature of the solvent.
Preferably the reaction is carried out in a solvent such as pyridine, chloroform, or dimethyl-sulfoxide, using from 2 to 10 equivalents of compound (V) for 1 equivalent of compound (II), and working at a temperature ranging from room temperature to 100°C.
When, in the compounds of formula (I'), A' and/or B' are different from A and/or B, the removal of the protective group for the primary and/or secondary amino functions is carried out following the procedures well known to those skilled in the art. Useful teachings can be found in Green, T.W., Wuts, P.G.M., "Protective Groups in Organic Synthesis", second Edition, John Wiley & Sons, 1991.
For example, the removal of the N-(tert-butoxycarbonyl) protective group can be performed by treatment of a compound of formula (I') with an excess of anhydrous hydrochloric acid in a solvent such as a (C,-C4) alkanol, dichloromethane, chloroform, or mixtures thereof, at a temperature of 0°C to the reflux temperature of the solvent and for a time ranging from several minutes to a few hours. Preferably the reaction is performed in 5 ethanol or in chloroform using from 10 to 20 molar equivalents of anhydrous hydrochloric acid at a temperature of from 20°C to 50°C, and is generally complete in four hours.
The compounds of formula (IV) are known or they 10 can be prepared according to known procedures, see for example, J. Med. Chem., 7, 493, (1964) and J. Het. Chem., 26, 85, (1989).
The compounds of formula (V) are known and commercially available, or they can be prepared according 15 to known procedures. r'or example, the preparation of some N-(tert-butoxycarbonyl) alkanediamines useful for the preparation of some compounds of the present invention is described in Synth. Comm., 20, 2559, (1990) or in J. Med.
Chem., 33, 97, (1990).
The compounds of formula (III) wherein Z = OTs [ compounds III' ) ) an be prepared by a multistep procedure, depicted in scheme 2, involving the following reactions:
(c) the Friedel and Craft acylation of 1,4-difluorobenzene with pyridine-3,4-dicarboxylic anhydrides (VI) where R6 is hydrogen or a suitable protecting group of the hydroxy function such as methoxy or benzyloxy, in presence of A1C13 (110°C, 22 h) which leads to the regioisomeric keto-acids (VIIa) and (VIIb);
(d) reaction of the ketoacids (VIIa) and (VIIb) with sodium methoxide in methanol (8.5 h, reflux) leading to the regioisomeric methoxy-substituted ketoacids (VIIIa) and (VIIIb); compounds (VIIIa) and (VIIIb) where R6 is hydrogen can be reacted as such in the following step;
when R6 is different from hydrogen, compound (VIIIa) is purified by crystallization and reacted as pure regioisomer;
. 2143853 (e) reduction of compounds (VIIIa) (R6 different from hydrogen) with Zn/Cu couple in 75% aqueous formic acid (15' room temperature, then 80°C, 2h) leading to (IX); when R6 is hydrogen, the acids (IXa) and (IXb) can be separated by chromatography yielding the pure isolated regioisomers (IXa) and (IXb);
(f) cyclization of the appropriate acid (IX) by heating a suspension of the compound in polyphosphoric acid at 110-120°C for 2 h leading to the benzo[g]isoquinoline (X);
(g) oxidation of the compound (X) to the corresponding dione (XI) by cerium ammonium nitrate in a mixture of acetonitrile and water (60°C, 2 h);
(h) removal of the methoxy group of the dione (XI) by aluminum chloride in methylene chloride (room temperature 2 h, then ref lux temperature 1. 5 h) leading to compounds (XII) which correspond to a mixture of 9-fluoro 6-hydroxy and 9-chloro-6-hydroxy-5,10-diones (XII) due to partial substitution of the leaving fluoride by means of A1C13; and (i) the final functionalization of the free hydroxy group of (XII) by means of toluenesulfonyl chloride in pyridine at room temperature, leads to the desired compounds ( I I I ) wherein Z = OTs [ compounds ( II I ) ] ;
when R6 is a protective group of the hydroxy function, it can be removed according to methods well known to the expert in the art, thus leading to compound (III) where R
is OH.
In a preferred embodiment of this invention, the preparation of intermediates (XI) is carried out by a multistep procedure depicted in scheme 3 and involving the following reactions:
- cyclization of the mixture of the regioisomeric keto-acids (VIIa) and (VIIb) with 20% oleum at 130-140°C to give the 6,9-difluorobenzo[g]isoquinolines (XIII);
- reaction of (XIII) with one equivalent of sodium methylate in a solvent such as methanol to give a mixture of intermediates (XI) which is separated into the single pure compounds (XIa) and (XIb) by recrystallization from a solvent and/or column chromatography. The pure intermediates (XIa) and (XIb) are then processed according to equation (h) and (i) of scheme 2 and then according to scheme 1 to give compounds (Ia) and (Ib), respectively.
In the preferred process of this invention which provides the compounds of formula (I) wherein X = C and Y = N, the 9-chloro-6-fluorobenzo[g]isoquinoline-5,10 diones of formula (III") are prepared by the multistep process depicted in scheme 4 and involving the following reactions:
- lithiation of 1-chloro-4-fluorobenzene with an alkyllithium reagent such as sec-butyllithium in THF
at -75°C to give 1-lithio-5-chloro-2-fluorobenzene (XIV);
- acylation of 1-lithio-5-chloro-2-fluorobenzene (XIV), generated in situ according to the above step, with pyridine-3,4-dicarboxylic anhydrides (VI) to give the mixture of keto-acids (XVa) and (XVb) which can be separated into the single pure compounds by recrystallization from a solvent or by sublimation;
- reduction of the pure keto-acid (XVa) with Zn/Cu couple or Zn powder in 75% aqueous formic acid (15' at room temperature, then 80°C, 2 hrs) leading to (XVI);
- oxidative cyclization of (XVI) with fuming sulfuric acid (20-30% SO3, 10', 130°C) to give the 9-chloro-6-fluorobenzo[g] isoquinoline-5,10-diones of formula (III'!).
. . , v 2i43s~~
Intermediates (III ") are then processed according to scheme 1 to give the compounds of formula (I) wherein X = C and Y = N.
BIOLOGICAL ACTIVITY OF COMPOUNDS OF THE INVENTION
The evaluation of the biological activity for the compounds of this invention was performed in vitro and in vivo following the protocols developed by the U.S.
National Cancer Institute.
The evaluation of the in vitro cytotoxic activity of the compounds of the invention was performed using a human colon adenocarcinoma cell line (Lovo) isolated from a metastatic nodule, and a subline expressing multidrug resistance. The subline is resistant to a number of antitumor agents, among which are doxorubicin, VP-16, and vincristine. This subline (named Lovo/DX) shows reduced accumulation of doxorubicin and overexpression of a protein (Grandi, M., Geroni, C., Giuliani, F.C., British J. Cancer, (1986), 54, 515). The compounds were tested according to the MTT assay (Mosman, T. "Rapid Colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assay", J. Immunol. Methods, (1983), 65, 55-63; Green, L.M., "Rapid colorimetric assay for cell viability;
application to the quantitation of cytotoxic and growth inhibitory lymphokines", J. Immunol. Methods, (1984), 70, 257-268) in comparison with mitoxantrone, and doxorubicin.
_143853 ICso (~9/ml) com ound LOVO LOVO/DX RI
_. O NH~N~CH~s 0.3 5.0 16.7 I I
N
I
N-N
Nliz O NH~NH~ 0.5 22.4 44.8 I
N-N
N(Ch4s)~
O NH~N(CH~)Z .5 ~ 0.9 1.8 i I I
N
I
N-N~N(CH~)i MITOXANTRONE Q,p4 0.9 22.5 DOXORUBICIN 0.9 66.6 74 In general, representative compounds of this invention were more cytotoxic than doxorubicin and as cytotoxic as mitoxantrone in the Lovo cell line. When mitoxantrone was tested in the Lovo/DX cell line, a resistance index RI (defined a the ratio of the ICS for the resistant line cell to the ICso for the sensitive cell line) as high as 22.5 was found, showing that this subline l0 does have an acquired resistance to mitoxantrone and ametantrone. On the other hand, some compounds of this invention, when tested in the same resistant subline, show no cross resistance with mitoxantrone and ametantrone as reported in Table 2. The in vitro evaluation of representative compounds of this invention suggests that representative compounds of this invention may be useful in order to overcome the multidrug resistance-mediated mechanism of tumor resistance.
~I43~53 Studies of the biological activity in vivo of representative compounds of the invention were performed using the P388 and L1210 marine leukemia models. P388 marine leukemia cells were intraperitoneally (ip) or 5 intravenously (iv) injected in CD2F1 mice. Treatment was initiated approximately 24 hours after tumor transplantation and dosages of the drug were administered ip (P388 ip/ip) or iv (P388 iv/iv) according to preestablished protocols, usually at 3-day (P388 iv/iv) or 10 4-day (P388 ip/ip) intervals. The studies were done over a 60-day period and the date of death for each animal was recorded. The % T/C was determined using the mean survival time (MST) for each group according to the formula ' 15 % T/C = [(MST treated) / (MST control)] x 100 Representative compounds of this invention were able to increase the survival time of treated animals significantly more than mitoxantrone, leading to higher T/C % values at well tolerated dosages. Moreover, the 20 above representative compounds of the invention showed antileukemic activity over a wide range of well tolerated dosages, and, in particular, were active at dosages which were lower than the maximum tolerated dose, providing indication for more favorable therapeutic index in comparison to mitoxantrone.
The antitumor activity of representative compounds of this invention was evaluated also in the L1210 marine leukemia model.
L1210 leukemia cells were intraperitoneally (ip) or intravenously (iv) injected in CDF1 mice and treatment was initiated approximately 24 hours after tumor transplantation. Dosages of the drugs were administered ip (L1210 ip/ip) or iv (L1210 iv/iv) according to preestablished protocols, usually at 3-day (L1210 iv/iv) or 4-day (L1210 ip/ip) intervals. The studies were done over a 60-day period and the date of death for each animal was recorded. The % T/C was determined using the mean survival timed (MST) for each group according to the formula:
% T/C [(MST treated) / (MST control)] x 100 Also in this further leukemia model, representative compounds of this invention showed activity superior to the clinically used antitumor drug mitoxantrone. Since representative compounds of this invention show good results against in vivo models of murine P388 and L1210 leukemias, which are considered to be predictive of antitumor activity in humans, the compounds disclosed herein are expected to be operative against human leukemias and solid tumors sensitive to treatment with antitumor antibiotics.
The compounds of the present invention may therefore be used as active ingredients of therapeutic compositions to induce regression and/or palliation of cancers in mammals when administered in amounts ranging from about 1 mg to about 0.4 g per kilogram of body weight. A preferred dosage regimen would be-from about 1 mg to about 50 mg per kilogram of body weight per day.
Unit dosage may be employed so that from about 70 mg to about 3.5 g of the active compound for a subject of about 70 kg of body weight are administered in a 24-hour period.
The dosage may be adjusted to be compatible to other treatment regimens, such as radiation therapy.
The pharmaceutical composition may be in the form of tablets, capsules, gel capsules, suppositories, lyophilized powders and solutions for intravenous administration. The invention is illustrated by the following non-limiting examples, and variations which are readily apparent to those skilled in the art.
21438.x:3 SYNTHESIS OF COMPOUNDS OF THE INVENTION
Preparative Example 1 Pyridine-3,4-dicarboxylic acid anhydride A mixture of pyridine 3,4-dicarboxylic acid (15.0 g) and acetic anhydride (30 mL) is refluxed for two hours. The excess acetic anhydride is removed by distillation and the anhydride is collected and purified by sublimation (123°C at 3 mm Hg) to yield pyridine 3, 4-dicarboxylic acid anhydride as a white solid ( 10. 1 g) .
m.p.. 74-76°C.
~H-NMR (CDC13): 7.94 (d, 1H); 9.24 (d, 1H); 9.39 (s, 1H).
Preparative Example 2 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl) isonicotinic acid A mixture of pyridine 3,4-dicarboxylic acid anhydride (5.0 g) and aluminum chloride (17.5 g) in 1,4-difluorobenzene (65 mL) is heated in an oil bath at 110°C
for 22 hours. The excess 1,4-difluorobenzene is recovered by distillation. The residue is cooled in an ice-bath and quenched with ice-water (75 mL) and concentrated hydrochloric acid (6.3 mL). The precipitated solid is filtered and dried to yield an approximately 4/1 mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl) isonicotinic acid respectively, as a white powder (7.7 g) which can be recrystallized from acetonitrile and water.
m.p.. 214-217°C.
'H-NMR (DMSO-db): 7.4 (m); 7.5 (m); 7.90 (m); 8.80 (d);
8.90 (d); 9.15 (s).
Recrystallization of this material (15.97 g) from absolute ethanol (360 mL) yields almost pure 3-(2,5-difluoro-benzoyl) isonicotinic acid (1.146 g).
_2143853 Preparative Example 3 4-(2-methoxy-5-fluorobenzoyl)nicotinic acid and 3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid The mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)isonicotinic acid of Preparative Example 2 (14.1 g) is added to a solution of sodium methylate, prepared by portionwise addition of sodium ( 6. 8 g) to dry methanol v ( 140 mL) . The reaction mixture is allowed to react at the reflux temperature for 8.5 hours and at room temperature overnight. The reaction mixture is concentrated to about one third of its volume, water (100 mL) is added and the remaining methanol is removed by distillation. Concentrated HC1 (25 mL) is slowly added to the residue while cooling at 10°C and the obtained precipitate is recovered by suction and washed with 0.1 N HC1, to give an approximately 4:1 mixture of 4-(2-methoxy-5-fluorobenzoyl) nicotinic acid and 3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid (11.31 g).
m.p.. > 230°C.
'H-NMR (DMSO-db): 3.40 (s); 3.45 (s); 7.15 (m); 7.37 (d);
7.42-7.63 (m); 7.26 (d); 8.60 (s); 8.83 (d); 9.07 (s), 13.55 (br.s).
Preparative Example 4 4-(2-methoxy-5-fluorobenzyl)nicotinic acid (and 3-(2-methoxy-5-fluorobenzyl)isonicotinic acid) Zinc-copper couple (L. F. Fieser and M. Fieser, Reagents for Organic Synthesis, Vol. 1, page 1292) (1.5 g) is added to a stirred suspension of the mixture of 4-(2-methoxy-5-fluorobenzoyl)nicotinic acid and3-(2-methoxy-5-fluorobenzoyl)isonicotinic acid of Preparative Example 3 (1.222 g) in formic acid (15 mL) and water (5 mL). After 15 minutes at room temperature the reaction mixture is heated for two hours in a oil bath held at 80°C. After cooling to room temperature the reaction mixture is . _2143853 filtered through a sintered glass filter and the solids are thoroughly washed with 75% aqueous formic acid ( 10 mL) and then with ethyl acetate (10 mL). The combined filtrates are concentrated to about 5 mL, treated with 0.5N HC1 (15 mL) and extracted with ethyl acetate (3 x 20 mL); finally they are saturated with sodium chloride and further extracted with ethyl acetate/1,2-dimethoxyethane 3/1 (2 x 20 mL). The combined organic phases are dried over anhydrous sodium sulphate and the l0 solvent removed under reduced pressure to give a yellowish residue. Subjecting this material to silica-gel column chromatography (eluant: ethyl acetate/methanol/acetic acid from 96/4/0 to 90/10/1 v/v/v) 4-(2-methoxy-5-fluorobenzyl) nicotinic acid (0.805 g) is obtained as a yellowish white solid.
m.p.. > 220°C.
~H-NMR (DMSO-db): 3.70 (s, 3H); 4.33 (s, 2H); 6.91-7.12 (m, 3H); 7.21 (d, 1H); 8.61 (d, 1H); 8.97 (s, 1H). From the above column-chromatography some 3-(2-methoxy-5-fluoro-benzyl)isonicotinic acid may also be recovered.
Preparative Example 5 9-fluoro-10-hydroxy-6-methoxybenzo[g]isoquinoline A mixture of 4-(2-methoxy-5-fluorobenzyl) nicotinic acid (0.63 g) and polyphosphoric acid (15 g) is heated at 110-120°C for two hours under stirring. The heating is removed and water (50 mL) is added to the reaction mixture while it is still warm (60°C). The mixture is cooled to 0°C, neutralized with 20% sodium hydroxide and allowed to stir at room temperature for 1.5 hours; finally it is extracted with 4% methanol in chloroform (4 x 75 mL). The combined organic phases are washed with brine, dried over anhydrous sodium sulphate and the solvents removed under reduced pressure to give 9-fluoro- 10-hydroxy-6-methoxybenzo[g] isoquinoline (0.40 g) as a purple-red solid.
m.p.. > 210°C (from ethanol).
.. . _2143853 ~H-NMR (DMSO-db) :3 .87 (s, 3H) ; 6.70-6.83 (m, 2H) ; 6.92-7.00 (m, 1H); 7.30 (d, 1H); 7.50 (d, 1H); 8.75 (s, 1H); 12.30 (br.s, 1H).
UV (ethanol) : lambda max. (nm) (E ,%) (cm) : 539 (204) ;
5 398 (513); 378 (452); 266 (1232).
IR (KBr): 729, 1245, 1499, 1528, 1620, 1644, and 2838 cm'.
Preparative Example 6 9-fluoro-6-methoxybenzo[g]isoquinoline-5,10-dione A solution of cerium ammonium nitrate (CAN;
10 13.70 g) in water (50 mL) is added during twenty minutes to a stirred suspension of 9-fluoro-10-hydroxy-6-methoxy-benzo[g]isoquinoline (1.22 g) in acetonitrile (150 mL).
At the end of the addition the obtained suspension is heated at 60°C for two hours to give a clear, dark 15 solution which is cooled to room temperature and diluted with water (100 mL). Following removal of acetonitrile by distillation at reduced pressure the aqueous phase is saturated with sodium chloride and extracted with methylene chloride (3 x 150 mL). The combined organic 2o solutions are dried over anhydrous sodium sulphate and the solvent is removed at reduced pressure. The obtained residue is purified by silica-gel column chromatography (eluant: methylene chloride/ethyl acetate from 85/15 to 75/25 v/v) to give 9-fluoro-6-methoxybenzo[g]
25 isoquinoline5,10-dione as a brown-yellow solid (0.48 g).
m.p.. > 220°C.
'H-NMR (CDC13) : 4.05 (s, 3H) ; 7.38 (dd, J=3.39, 9.39 Hz, 1H); 7.55 (dd, J=10.37, 9.39 Hz, 1H), 8.00 (dd, J=5.09, 0.78 Hz, 1H); 9.07 (d, J=5.09 Hz, 1H); 9.45 (d, J=0, 78 Hz, 1 H).
Preparative Example 7 6,9-difluorobenzo[g]isoquinoline-5,10-dione A solution of the mixture of 4-(2,5-difluoro-benzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)iso-nicotinic acid of Preparative Example 2 (61.07 g) in 20%
oleum (100 mL) is heated at 140°C while 20% oleum is added in four portions (13.2 mL each) at 20 min-intervals.
After the fourth addition the mixture is heated for 20 l0 min, then it is cooled to room temperature and quenched with a mixture of ice (1,500 g), water (1,500 mL) and 35%
NaOH (350 mL). The mixture is extracted four times with methylene chloride (1 x 1,000 mL followed by 3 x 500 mL).
The combined organic solutions are washed with water (2 x 1,000 mL), dried (NazS04) and the solvent removed by roto-evaporation. The dark-red solid obtained (56.0 g) is dissolved in boiling THF (840 mL) and decolorizing charcoal (8.40 g) is added. After 30 min the mixture is filtered while hot and the filtrate concentrated to ~20 200 mL. The precipitate obtained is collected by suction filtration to give 6,9-difluorobenzo[g]isoquinoline-5,10-dione (43.00 g) .
m.p.. 201-203°C.
Concentration of the mother liquor to 70 mL yields a second crop of product (3.35 g), m.p. 200-202°C.
Preparative Example 8 9-fluoro-6-methoxybenzo[g]isoquinoline-5,10-dione and 6-fluoro-9-methoxybenzo[g]isoquinoline-5,10-dione A solution of sodium methylate is prepared under a nitrogen atmosphere in a dropping addition funnel from dry methanol (97.6 mL) and sodium (2.024 g) portionwise added. When all the sodium disappears the solution is dropped during 2 h, 35 min to a stirred solution of 6,9-difluorobenzo[g]isoquinoline-5,10-dione of Preparative Example 7 (19.615 g) in dry THF (883 mL) at 20°C. At the end of the addition the solution is concentrated to half its volume by roto-evaporation, then it is cooled to 18°C
for 30 min. The solid which separates is recovered by suction filtration and washed with THF (100 mL); then it is suspended in water (80 mL) under stirring overnight and filtered again to give the solid A (7.4 g).
The mother THF solution is concentrated to dryness. The obtained solid is suspended in water (78 mL) under stirring for 1 hour and filtered to give the solid B (12.9 g).
The solid A (9.30 g) in methylene chloride (45 mL) is heated to reflux for 30 min. After cooling to room temperature the solid is recovered by suction filtration, washed with methylene chloride (5 x 3 mL) and dried under vacuum at 40°C to give 6-methoxy-9-fluorobenzo[g)iso-quinoline-5,10-dione (8.65 g) as a pure compound.
m.p.. 248-250°C.
~H-NMR (CDC13) : 4.05 (s, 3H) ; 7.40 (dd (J=9.39, 3.91 Hz) 1H); 7.55 (dd, J=10.37, 9.39 Hz, 1H); 8.00 (dd, J=5.09, 0.78 Hz, 1H); 9.05 (d, J=5.09 Hz, 1H); 9.48 (d, J=0.78 Hz, 1H) .
The solid B (14.0 g) is dissolved in methylene chloride (140 mL) and the insoluble portion is removed by filtration. The methylene chloride solution is applied on a silica gel (630 g) column chromatography, which is eluted at ambient pressure with methylene chloride. When the yellow chromatographic bands appear well separated the column is eluted with mixtures of methylene chloride/ethyl acetate from 10/1 to 8/2, to 1/1 to give a 94/6 mixture (HPLC evaluation) of 9-methoxy-6-fluorobenzo[g] iso-quinoline-5,10-dione and 6-methoxy-9-fluorobenzo[g] iso-quinoline-5,10-dione respectively (6.50 g).
m.p.. 168-170°C.
~~ 2143853 Preparative Example 9 a) 9-fluoro-6-hydroxybenzo[gJisoquinoline-5,10-dioneand 9-chloro-6-hydroxybenzo[g]isoqu:inoline-5,10-dione (1/1 mixture: small scale reaction) A mixture of 9-fluoro-6-methoxybenzo[gJ iso-quinoline-5,10- dione (0.072 g) and aluminum trichloride (0.112 g) in dry methylene chloride (40 mL) is stirred at room temperature for 4 hours under a nitrogen atmosphere.
An additional portion of aluminum chloride (0.190 g) is l0 added and the mixture is allowed to react at reflux for 1.5 hrs and at room temperature overnight. Following addition of brine (15 mL) the aqueous phase is separated and extracted with methylene chloride (3 x 5 mL). The combined organic solutions are dried over anhydrous sodium sulphate and the solvent is removed by distillation at reduced pressure to give an approximately 1:1 mixture (0.070 g) of 9-fluoro-6-hydroxybenzo[g] isoquinoline-5,10-dione (slower moving yellow spot on silica gel TLC
plate, eluant methylene chloride/ethyl acetate 70/30) and 9-chloro-6-hydroxybenzo [g]isoquinoline-5,10-dione (faster moving yellow spot on the above chromatographic system) which is used without further purification for the next step.
9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione has the following 'H-NMR spectrum (CDC13):
7.38 (dd, 1H); 7.53 (dd, 1H); 8.09 (dd, 1H); 9.15 (d, 1H);
9.57 (d, 1H); 12.56 (s, 1H).
9-chloro-6-hydroxybenzo[g]isoquinoline-5, 10-dione has the following 'H-NMR spectrum (CDC13) :
7.91 (d, 1H); 7.75 (d, 1H); 8.07 (dd, 1H); 9.13 (d, 1H); 9.58 (d, 1H); 12.95 (s, 1H).
_2143853 b) 9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneand 9-chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione(9/1 mixture: multigram preparation):
Aluminum chloride (19.05 g) is added in one portion to a stirred refluxing solution of 6-methoxy-9-fluorobenzo(g]isoquinoline-5,10-dione (7.20 g) in methylene chloride (432 mL). After refluxing for 4 hours the reaction mixture is cooled and poured in water (1,300 mL). Methylene chloride (200 mL) is added and after l0 stirring for 10 min the organic phase is separated. The aqueous solution is saturated with NaCl and further extracted with methylene chloride (3 x 400 mL). The combined organic solutions are washed with brine (1,000 mL), dried and the solvent removed by roto-evaporation.
The brown solid obtained (6.5 g) is recrystallized from ethyl acetate/n-hexane 1/1 (65 mL) to yield a 9/1 mixture ('H-NMR evaluation) of 9-fluoro-6-hydroxybenzo[g] iso-quinoline-5,10-dione and 9-chloro-6-hydroxybenzo[g] iso-quinoline-5,10-dione respectively (6.00 g).
m.p.. partial melting at 179-181°C; complete melting at 193-195°C.
Preparative Example 10 a) 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline 5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]isoquinoline-5,10-dione (1/1 mixture; small scale preparation) The 1:1 mixture of 9-fluoro-6-hydroxybenzo[g]
isoquinoline- 5,10-dione and 9-chloro-6-hydroxybenzo[g]
isoquinoline-5,10-dione, of Preparative Example 9a, (0.060 g) is dissolved in dry pyridine (2 mL) and p-toluene-sulfonyl chloride (0.095 g) is added. After stirring at room temperature for one hour, triethylamine (0.25 mL) is added and stirring is continued for one additional hour.
The reaction mixture is concentrated almost to dryness and . . 2143853 partitioned between 1 N HC1 ( 4 mL) -20% ammonium sulfate ( 6 mL) and ethyl acetate (l0 mL). The aqueous phase is separated, extracted with ethyl acetate (3 x 5 mL) and discarded. The combined organic solutions are dried over 5 anhydrous sodium sulphate and concentrated to dryness to give an approximately 1:1 mixture (0.095 g) of 9-fluoro-6-(p-toluenesulfonyloxy) benzo[g) isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]iso-quinoline-5,10-dione which is used without further 10 purification for the next step.
The pure single compounds can be obtained by silica-gel column chromatography of this mixture (eluant:methylene chloride/n-hexane/ethyl acetate from 50/45/5 to 50/40/10 v/v/v) and they have the following 15 analytical data:
9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]iso-quinoline-5,10-dione: m.p. 173-174°C.
~H-NMR (CDC13): 2.45 (s, 3H), 7.35 (d, 2H); 7.50-7.57 (m, 2H); 7.82-7.94 (m, 3H); 9.08 (d, 1H); 9.48 (s, 1H).
20 9-chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5, 10-dione:
m.p.. 180-181°C.
~H-NMR (CDC13): 2.45 (s, 3H); 7.35 (d, 2H); 7.47 (d, 1H);
7.78-7.91 (m, 4H), 9.07 (d, 1H); 9.48 (s, 1H).
25 b) 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g)isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo [g)isoquinoline -5,10-dione (9/1 mixture; multigram preparation):
Triethylamine (8.20 mL) is added to a stirred 30 suspension of the 9/1 mixture of 9-fluoro-6-hydroxy-benzo[g]isoquinoline-5,10-dione and 9-chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione respectively of Preparative Example 9b (5.53 g) and p-toluenesulfonyl-chloride (8.47 mL) in methylene chloride (166 mL). The reddish-violet solution obtained is left at room temperature under a nitrogen atmosphere for 1 hour and then it is poured into water (500 mL). The organic phase is separated and the aqueous solution is further extracted with methylene chloride (100 mL). The combined organic solutions are dried (NazS04) and concentrated to dryness.
The obtained solid is suspended in n-hexane (100 mL) for 1 hour and filtered to give a 9:1 mixture (~H-NMR
evaluation) of 9-fluoro-G-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluene sulfonyloxy)benzo [g]isoquinoline-5,10-dione respectively (8.85 g) .
m.p.. 156-158°C.
Preparative Example 11 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid and 4-(5-chloro-2-fluorobenzoyl)nicotinic acid Sec-butyllithium (1.3 M in cyclohexane; 6.0 mL) is added dropwise via a syringe to a stirred solution of 1-chloro-4-fluorobenzene (0.97 g) in THF (70 mL) at -75°C
which is kept under a nitrogen atmosphere. After stirring for additional 30 min, the yellow mixture is transferred dropwise via a jacketed canula into a stirred mixture of pyridine-3,4-dicarboxylic acid anhydride (1.00 g) in THF
(100 mL) at -78°C under a nitrogen blanket. The pale yellow solution is allowed to warm to -20°C for 4 hours.
The THF is removed at reduced pressure. The yellow solid obtained is dissolved in water (10 mL), cooled to 0°C, and acidified with dilute HC1 in an ice-bath and the resulting precipitate is collected by filtration. Upon heating the white solid with acetone (30 mL), an insoluble material remains (0.095 g), which by ~H-NMR analysis is a 94/4 mixture of 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid and 4-(5-chloro-2-fluorobenzoyl)nicotinic acid, respectively.
m.p.. 289-291°C.
After centrifugation, the supernate is removed and roto-evaporated to give crystals of a 94/6 mixture (by ~H-NMR analysis) of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid respectively (0.947 g).
m.p.. 236-237°C.
Sublimation of this mixture (0.025 g) at 180 205°C/0.5 mm Hg gives a white solid with a 98/2 ratio of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5 chloro-2-fluorobenzoyl)isonicotinic acid respectively (20 mg) .
4-(5-chloro-2-fluorobenzoyl)nicotinic acid: 'H
NMR (CDC13/CD30D 9/1) : 6.96 (m, 1H) ; 7.21 (d, 1N) ; 7.45 (m, 1H); 7.86 (m, 1H); 8.76 (d, 1H); 9.18 (s, 1H).
3-(5-chloro-2-fluorobenzoyl)isonicotinic acid:
'H-NMR (DMSO-d6) : 7. 37 (m, 1H) ; 7.75 (m, 2H) ; 7. 83 (d, 1H) ;
8.77 (s, 1H); 8.90 (d, 1H).
Preparative Example 12 4-(5-chloro-2-fluorobenzyl)nicotinic acid Zinc-copper couple (0.75 g) is added to a stirred mixture of 4-(5-chloro-2-fluorobenzoyl)nicotinic acid and 3-(5-chloro-2-fluorobenzoyl)isonicotinic acid of Preparative Example 11 (94/6 on a molar base; 0.60 g) in 75% formic acid. The exothermic and effervescent reaction mixture is stirred for 15 min before heating to 80°C for 2 hours. After cooling to 40°C, the mixture is filtered through a sintered glass funnel. The solid is washed with 75% formic acid (1 x 5 mL) and ethyl acetate (2 x 5 mL).
The mixture is concentrated by roto-evaporation to about 2 mL. The orange oil obtained is dissolved in 0.5 N HCl (3 mL) and extracted with ethyl acetate (3 x 10 mL), then saturated with NaCl and extracted with ethyl acetate/1,2-dimethoxyethane (2 x 5 mL). The combined extracts are dried with Na2S04 and the solvents removed by roto-evaporation to yield a yellow foam. The foam (0.541 g) is recrystallized in hot acetonitrile (1 mL) to yield 4-(5-chloro-2-fluorobenzyl)nicotinic acid (0.142 g).
m.p.. 174-176°C.
~H-NMR (CDC13/CD30D 9/1): 4.43 (s, 2H); 6.79 (m, 1H); 6.86 (m, 1H); 6.95 (m, 1H); 7.11 (d, 1H); 8.55 (d, 1H); 9.12 (s, 1H).
Preparative Example 13 9-chloro-6-fluorobenzo[g]isoquinoline-5,10-dione Fuming sulfuric acid (30% S03; 0.31 mL) is added to 4-(5-chloro-2-fluorobenzyl)nicotinic acid of Preparative Example 12. The dark mixture is heated quickly to 130°C for 10 min in a flask fitted with a cotton filled drying tube. After cooling to room temperature, the reaction mixture is quenched with ice (3 g) and extracted with methylene chloride (4 x 7 mL).
The combined extracts are dried with Na2S0~ and the solvent is removed by roto-evaporation to yield 9-chloro-6-fluoro-benzo[g]isoquinoline-5,10-dione as a yellow solid (0.045 g; 82% yield).
m.p.. 204-206°C.
~H-NMR (CDC13): 7.45 (m, 1H); 7.83 (m, 1H); 7.98 (d, 1H);
9.08 (d, 1H) ; 9.49 (s, 1H) .
Example 1 5-(p-toluenesulfonyloxy)-2-methylisoquino[8,7,6-cdJindazole-6(2H)-one The 1:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy) benzo[g] isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo[g]isoquinoline-5,10-dione, of Preparative Example 10a, (0.041 g) is dissolved in dry pyridine ( 2 mL) and a freshly prepared 1M
solution of N-methyhydrazine in pyridine (0.183 mL) is added. After stirring for three hours at room temperature the reaction mixture is concentrated to dryness and added with water (5 mL), with NaH2P04 saturated solution (5 mL) and extracted several times with methylene chloride (50 mL). The combined organic solutions are dried ever anhydrous sodium sulfate and the solvent is removed at reduced pressure. The obtained residue is purified by silica-gel column chromatography (eluant: methylene chloride/ethyl acetate 90/10 v/v (50 mL), then 75/25 (50 mL), then 60/40 (50 mL) and finally 40/60 (50 mL) to give2-methyl-5-(p-toluenesulfonyloxy)isoquino[8,7,6-cd]
indazole-6(2H)-one.
~H-NMR (CDC13): 2.42 (s, 3H); 4.25 (s, 3H); 7.33 (d, 2H);
7.53 (d, 1H); 7.63 (d, 1H); 7.95 (d, 2H); 8.07 (d, 1H) 8.80 (d, 1H); 9.50 (s, 1H).
Example 2 2-[2-(dimethylamino)ethyl)]-5-(p-toluenesulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-one Under a nitrogen atmosphere a solution of 2-(dimethylaminoethyl)hydrazine (J. Med. Chem. 7, 493, 1964) (1.86 g) in anhydrous THF (6.0 mL) is added during 30' to the stirred 9:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy) benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (2.4 g) in THF (24 mL) containing N,N-diisopropylethylamine (1.10 mL). A
slightly exothermic reaction ensues, and the reaction temperature increases from 20°C to 25°C. After one hour at room temperature the reaction mixture is poured in water (240 mL) and the suspension obtained is stirred for 30' . The solid is separated by suction, washed with water and dried at 40°C to give 2-[2-(dimethylamino)ethyl)]-5 (p-toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6(2H)-one (1.44 g).
m.p.. 139-141°C.
'H-NMR (CDC13): 2.35 (s, 6H); 2.45 (s, 3H); 2.95 (t, 2H);
4.65 (t, 2H); 7.35 (d, 2H); 7.52 (d, 1H); 7.80 (d, 1H);
7.95 (d, 2H); 8.10 (d, 1H); 8.80 (d, 1H); 9.55 (s, 1H).
2143$53 Example 3 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluene-sulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-one (2-N-tert-butoxycarbonylaminoethyl)hydrazineis 5 prepared by reaction of N-t-butoxycarbonyl-2-chloro-ethylamine with hydrazine following a procedure adapted from J. Med. Chem. 7, 493, (1964). Under a nitrogen r atmosphere a solution of (2-N-tert-butoxycarbonyl aminoethyl)hydrazine (9.2 g) in anhydrous THF (10 mL) is 10 added during 30' to the stirred 9:1 mixture of 9-fluoro-6 (p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneand 9-chloro-6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (3.0 g) in THF (25 mL) containing N,N-diisopropylethylamine (1.38 mL). A
15 slightly exothermic reaction ensues, and the reaction temperature increases from 21°C to 24°C. After stirring for one hour at room temperature the obtained precipitate is recovered by suction, washed with THF/n-hexane 1/1 (15 mL) and dried at 40°C under vacuum, to give 2-[2-(N-tert-2o butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one (1.33 g).
m.p.. 206-208°C.
~H-NMR (CDC13) : 1.4 (s, 9H) ; 2.45 (s, 3H) ; 3.75 (q, 2H) ;
4.70 (t, 2H); 4.92 (br, 1H); 7.35 (d, 2H); 7.50 (d, 1H);
25 7.75 (d, 1N); 7.95 (d, 2H); 8.09 (d, 1H); 8.78 (d, 1H);
9.50 (s, 1H).
Example 4 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluene-sulfonyloxy) isoquino[8,7,6-c]indazole-6(2H)-one 30 A solution of 2-[(2-hydroxyethylamino)ethyl]-hydrazine (J. Het. Chem., 26, 85, (1989); 0.179 g) in absolute ethanol (0.5 mL) is dropped into a stirred solution of the 9:1 mixture of 9-fluoro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-~143~~3 6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example lOb (0.200 g) in THF (2.0 mL) containing triethylamine (0.073 mL). After stirring for 2 hours at room temperature an additional amount of 2- [ ( 2-hydroxyethylamino)ethyl]hydrazine (0.179 g) in absolute ethanol (0.5 mL) is added and after two additional hours the reaction mixture is concentrated to the volume of about 1 mL. Water (20 mL) is added and the mixture is allowed to stir at room temperature overnight. The l0 precipitate is collected by suction filtration, dried under vacuum at 40°C and finally sludged in boiling ethyl acetate to give 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluenesulfonyloxy)isoquino[8,7,6-c]indazole-6(2H)-one (0.060 g).
m.p.. 131-133°C.
~H-NMR (DMSO-db/D20) : 2. 45 (s, 3H) ; 2 . 62 (t, 2H) ; 3. 13 (t, 2H); 3.40 (t, 2H); 4.65 (t, 2H); 7.25 (d, 1H); 7.40 (d, 2H); 7.75 (d, 2H); 7.95 (d, 1H); 8.15 (d, 1H); 8.80 (d, 1H); 9.40 (s, 1H).
Example 5 Preparation of 2-(aminoalkyl)-5-(p-toluenesulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-ones Using the procedure of Examples 1-4, the following compounds are obtained by reaction of the mixtures of 9-fluoro-6-(p-toluenesulfonyloxy) benzo[g]
isoquinoline-5,10-dione and 9-chloro-6-(p-toluene-sulfonyloxy)benzo[g]isoquinoline-5,10-dione of Preparative Example 10, with a substituted hydrazine selected from the group of 2-(diethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 3-dimethylaminopropylhydrazine [J. Het.
Chem., 23, 1491, (1986)], 2-aminoethylhydrazine [J. Het.
Chem., 23, 1491, (1986)], 2-(methylaminoethyl)hydrazine, 2-hydroxyethylhydrazine, 3-aminopropylhydrazine [J. Het.
Chem., 23, 1491, (1986)];
2-[2-(diethylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one;
2-[3-(dimethylamino)propyl]-5-(p-toluenesulfonyloxy)iso-q a i n o [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[2-(amino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[2-(methylamino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [ 8 , 7 , 6 - c d ] i n d a z o 1 a - 6 ( 2 H ) - o n a ;
2-[3-(amino)propyl]-5-(p-toluenesulfonyloxy)isoquino [8,'7,6-cd]indazole-6(2H)-one.
Example 6 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one A solution of methyl hydrazine (0.76 M; 0.021 g) in pyridine (0.6 mL) is added dropwise over two min to a stirred solution of9-chloro-6-fluorobenzo[g]isoquinoline-5,10-dione of Preparative Example 13 in pyridine (0.5 mL) cooled with an ice-bath. A yellow precipitate appears in the dark solution after 6 min. After 1.3 h the reaction mixture is reduced to half its volume by a gentle stream of nitrogen and quenched with ice (5 g). The pale yellow precipitate is collected by suction filtration and washed with ice-water (2 x 1 mL) and dried under vacuum. The yellow solid is purified by silica gel column chromatography (eluant: chloroform/methanol 96/4 v/v) to yield 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.033 g; 71% yield) as a yellow solid.
m.p.. 244-245°C.
~H-NMR (CDC13): 4.25 (s, 3H); 7.59 (dd, 2H); 7.92 (d, 1H);
8.84 (d, 1H); 9.55 (s, 1H).
Example 7 Preparation of 2-(aminoalkyl)-5-chloroisoquino[5,6,7-cd]indazole-6(2H)ones Using the procedure of Example 6 the fdllowing compounds are obtained by reaction of 9-chloro-6-fluorobenzo[g]isoquinoline-5,1o-dione of Preparative Example 13 with a substituted hydrazine selected from the r _~~43853 group of (2-N-tert-butoxycarbonylaminoethyl) hydrazine, 2- -(dimethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 2- -(diethylaminoethyl)hydrazine [J. Med. Chem., 7, 493, (1964)], 2-[(2-hydroxyethylamino)ethyl]hydrazine (J.
Het. Chem., 26, 85, (1989)], 3-dimethylaminopropyl-hydrazine [J. Het. Chem., 23, 1491, (1986)], 2-amino-ethylhydrazine [J. Het. Chem., 23, 1491, (1986)], 2-(methylaminoethyl)hydrazine, 2-hydroxyethylhydrazine, 3- -aminopropylhydrazine [J. Het. Chem., 23, 1491, (1986)];
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-chloroisoquino [5,6,7-cd]indazole-6(2 H)-one;
m.p.. 226-228°C.
~H-NMR (CDC13 + CD~OD) : 1. 30 (s, 9H) ; 3.58 (t, 2H) ; 4.63 (t, 2H); 7.54 (d, 1H); 7.70 (d, 1H); 7.90 (dd, 1H); 8.70 (d, 1H); 9.40 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
m.p.. 160-161°C.
~H-NMR (CDC13): 2.32 (s, 6H); 2.95 (t, 2H); 4.65 (t, 2H);
7.60 (d, 1H); 7.69 (d, 1H); 8.00 (dd, 1H); 8.88 (d, 1H);
9.60 (s, iH);
2-[2-(diethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(diethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one;
m.p.. 148-152.5°C.
~H-NMR (CDC13 + CD30D) : 2.75 (t, 2H) ; 3. 43 (t, 2H) ; 3. 60 (t, 2H) ; 4. 63 (t, 2H) 7. 55 (d, 1N) ; 7 .75 (d, 1H) ; 7.98 (dd, 1H); 8.73 (d, iH); 9.40 (s, 1H);
2-[3-(dimethylamino)propyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(amino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
2-[2-(methylamino)ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one;
2-[2-(hydroxy)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
2-[3-(amino)propyl]-5-chloroisoquino[5,6,7-cd]indazole-6 (2H)-one;
Example 8 5-[[2-(dimethylamino)ethyl]amino)-2-methylisoquino[8,7,6-cd]indazole-6(2H)-one A 1M solution of N,N-dimethylethylenediamine in pyridine (0.10 mL) is added to a stirred suspension of 2-l0 methyl-5- (p-toluenesulfonyloxy)isoquino [8,7,6-cd]
indazole-6(2H)-one (0.02 g) in dry pyridine (2 mL). After stirring at room temperature for one hour the reaction mixture is heated at 70°C for 13 hours while additional amounts of N,N-dimethylethylenediamine solution (0.1;
0.05; 0.05 mL) are added after 2, 4 and 11 hours respectively. Pyridine and excess N,N-dimethylethyl-enediamine are removed by distillation at reduced pressure and the obtained residue is partitioned between CH2C12 (50 mL) and brine (10 mL) to which NaHC03 saturated solution is added (1 mL). The organic solution is dried over anhydrous Na2S04 and the solvent removed by distillation.
The orange residue obtained is purified by silica-gel column chromatography (eluant: CHC13/MeOH 95/5 (30 mL) followed by CHC13/MeOH/NH,~OH 90/15/0.5 (50 mL) to give 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino [8,7,6-cd] indazole-6(2H)-one (0.011 g) as a reddish orange solid.
m.p.. 208-215°C (dec.).
'H-NMR (CDC13): 2.40 (s, 3H); 2.75 (t, 2H); 3.57 (q, 2H);
4. 25 (s, 3N) ; 6.97 (d, 1H) ; 7. 63 (d, 1N) ; 8. 30 (dd, 1H) 8.79 (d, 1H) ; 9.30 (br.t, 1H) ; 9.62 (d, iH) .
_2143853 Example 9 2-[2-(dimethylamino)ethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[8,7,6-cd]indazole-6(2N)-one A solution of 2-[2-(dimethylamino)ethyl]-5-(p-5 toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6 (2H)-one of Example 2 (0.463 g) and 2-(dimethylamino)ethylamine (0.80 mL) in dry pyridine (4.63 mL) is heated at 80°C for 1 h, 30~ under a nitrogen blanket. The solution is then concentrated to dryness and the dark residue obtained is 10 partitioned between brine (30 mL) and ethyl acetate (4 x 25 mL). The combined organic solutions are dried over Na2S04 and concentrated to about 3 mL. After addition of n-hexane (12 mL) and stirring for one hour the precipitate is collected by suction and dried at 40°C
15 under vacuum to give 2-[2-(dimethylamino)ethyl)]5-[[2-(dimethylamino) ethyl]amino] isoquino[8-,7,6-cd]indazole-6(2H)-one (0.23 g).
m.p.. 150-152°C.
~H-NMR (CDC13): 2.32 (s, 6 H); 2.40 (s, 6H); 2.70 (t, 2H);
20 2 . 95 (t, 2H) ; 3 . 60 (q, 2H) ; 4 . 65 (t, 2H) ; 6. 98 (d, 1H) ;
7.70 (d, 1H); 8.30 (d, iH); 8.80 (d, 1H); 9.30 (br, 1H);
9.65 (s, 1H).
Example 10 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(N-tert-25 butoxycarbonylamino)ethyl]amino]isoquino[8,7,6-cd]
indazole-6(2H)-one A suspension of 2-[2-(N-tert-butoxycarbonyl-amino)ethyl]-5-(p-toluenesulfonyloxy)isoquino(8,7,6-cd]
indazole-6(2H)-one of Example 3 (0.535 g) and N-(tert-30 butoxycarbonyl)ethylenediamine (prepared according to Synt. Comm., 20, 2559, (1990); 1.12 g) in dry pyridine (5.35 mL) is heated at 80°C. The dark solution obtained is held at this temperature for 5 hours, then it is concentrated to dryness and partitioned between brine (30 35 mL) and ethyl acetate (2 x 25 mL). The orange-red solid insoluble in the biphasic mixture is separated by suction filtration and dried at 40°C under vacuum (0.43 g).
This material (0.60 g) is purified by column chromatography (Si02; eluant methylene chloride/methanol from 90/10 to 70/30 v/v). The fractions containing the product are pooled and concentrated to about 20 mL and 2 [2-(N-tert-butoxy carbonylamino)ethyl]-5-[[2-(N-tert butoxycarbonylamino) ethyl]amino]isoquino[8,7,6-cd]
indazole-6(2H)-one separates as red-orange crystals (0.45 g).
m.p.. 211-213°C.
~H-NMR (CDC13/DMSO-db 9/1): 1.3 (s, 9H); 1.4 (s, 9H); 3.32 (q, 2H); 3.58 (m, 4Hj; 4.58 (t, 2H); 6.20 (br, 1H); 6.4a (br, 1H); 7.05 (d, 1H); 7.70 (d, 1H); 8.15 (d, 1H); 8.65 (d, 1H); 9.20 (br, 1H); 9.49 (s, 1H).
Example 11 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[(2-(dimethyl-amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one A suspension of 2-[2-(N-tert-butoxycarbonyl-aminojethyl]-5-(p-toluenesulfonyloxy) isoquino[8,7,6- cd]
indazole-6(2H)-one (0.056 g) and 2-(dimethylamino) ethylamine (0.080 mL) in dry pyridine (0.50 mL) is heated at 80°C. The dark solution obtained is held at this temperature for 1 hour, then it is left at room temperature overnight. The dark precipitate obtained is separated by suction and purified by column chromatography (Si02; eluant ethyl acetate and then methylene chloride/methanol 9/0.5 v/v) to give 2-[2-(N-tert-butoxy-carbonylamino)ethyl)-5-[[2-(dimethylamino) ethyl) amino]
isoquino[8,7,6-cd]indazole-6(2H)-one (0.024 g) as a red-orange solid.
m.p.. 225-227°C (from methylene chloride).
~H-NMR (CDC13) : 1.43 (s, 9H) ; 2.40 (s, 6H) ; 2.7 (t, 2H) ;
3.55 (q, 2H); 3.78 (m, 2H); 4.65 (t, 2H); 5.23 (br.m, 1H);
6.87 (d, 1H); 7.62 (d, 1H); 8.28 (dd, 1H); 8.76 (d, 1H);
9.6 (s, 1H).
_2143853 Example 12 isoquino[8,7,6-cd]indazole-6(2H)-ones Following the procedures of Examples 8-11, the following compounds are prepared by reaction of 2-[2-(dimethylamino)ethyl]-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6 (2H)-one of Example 2, 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy)iso-quino[8,7,6 -cd]indazole-6(2H)-one of Example 3, or 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-(p-toluenesulfonyloxy) isoquino[8,7,6-c] indazole-6(2H)-one of Example 4 with the properly selected amine:
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxy-ethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 3.25 (m, 6H); 3.61 (t, 4H); 3.71 (m, 4H);
3.98 (q, 2H); 4.65 (t, 2H); 5.31 (br, 2H); 7.08(d, 1H), 7.70 (d, 1H); 8.30 (d, 1H); 8.83 (d, 1H); 9.30 (br, 1H);
9.69 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[3-(amino)propyl]a mino] isoquino[8,7, 6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.05 (m, 2H); 3.18 (m, 4H); 3.58 (t, 2H);
3.65 (t, 2H); 3.78 (q, 2H); 4.62 (t, 2H); 5.20 (br, 3H), 7.10 (d, 1H); 7.69 (d, 1H); 8.30 (d, 1H); 8.85 (d, 1H);
9.15 (br, 1H); 9.30 (t, 1H); 9.71 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[8,7, 6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 3.20 (m, 4H), 3.58 (t, 2H); 3.66 (t, 2H);
3.86 (q, 2H); 4.61 (t, 2H); 5.15 (br, 3H); 7.12(d, 1H);
7.69 (d, 1H); 8.30 (d, 1H); 8.85 (d, 1H); 9.15 (br, 1H);
9.30 (t, 1H); 9.71 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquin o[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.61 (s, 3H); 3.06 (t, 2H); 3.20 (t, 2H);
3.58 (t, 2H); 3.67 (t, 2H); 3.88 (q, 2H); 4.65 (t, 2H);
5. 10 (t, 1H) ; 7 (d, 1H) ; 7 .70 (d, 1H) ; (d, 1H) . 05 8. 33 ;
8.81 (d, 1H); 8.99 (br, 2H); 9.35 (t, 1H); 9.66(s, 1H).
2-[2-[(2-hydroxyethylamino]ethyl]-5-[[2-(dimethylamino) ethyl] amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13): 2.42 (s, 6H); 2.75 (t, 2H); 3.18 (t, 2H);
3.58 (q, 2H); 3.63 (t, 2H); 3.68 (t, 2H); 4.61 (t, 2H);
5. 15 (t, 1H) ; 6.99 (d, 1H) ; 7 . 66 (d, 1H) ; 8. 31 (d, 1H) ;
8.80 (d, 1H); 9.11 (br, 1H); 9.35 (t, 1H), 9.65 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(N-tert-butoxy-carbonylamino)ethyl]amino]isoquino[8,7,6-cd] indazole-6 (2H)-one;
'H-NMR (CDC13 + CD30D) : 1.40 (s, 9H) ; 3: 31 (m, 4H) ; 3.52 (q, 2H); 3.63 (t, 2H); 3.85 (t, 2H); 4.71 (t, 2H); 7.03 (d, 1H); 7.70 (d, 1H); 8.21 (dd, 1H); 8.76 (d, 1H); 9.61 (s, 1H) .
2-[2-(N-tert-butoxycarbonylamino)ethy)]-5-[[2-[(2 hydroxyethyl)amino]ethyl]amino]isoquino[8,7,6-cd]indazole 6(2H)-one 'H-NMR (CDC13 + CD30D) : 1.45 (s, 9H) ; 3. 18 (m, 4H) ; 3 .73 (q, 2H); 3.80 (m, 4H); 4.67 (t, 2H); 7.00 (d, 1H); 7.68 (d, 1H); 8.25 (dd, 1H); 8.75 (d, 1H); 9.60 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
m.p.. 156-157°C.
'H-NMR (CDC13): 2.30 (s, 6H); 2.91 (m, 4H); 3.08 (t, 2H);
3.60 (t, 2H); 3.75 (m, 2H); 4.60 (t, 2H); 6.90 (d, 1H);
7.60 (d, 1H); 8.25 (dd, 1H); 8.75 (d, 1H); 9.45 (br, 1H);
9.60 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2. 30 (s, 6H) ; 2.95 (t, 2H) ; 3. 13 (t, 2H); 3.65 (t, 2H); 4.58 (t, 2H); 7.04 (d, 1H); 7.70 (d, 1H); 8.18 (dd, iH); 8.66 (d, 1H); 9.51 (s, 1H).
. _ 2143853 Example 13 5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one 5-chloro-2-methylisoquino[5,6,7-cd]indazole-6 (2H)-one of Example 6 (0.013 g) is added to 2-(dimethyl-amino)ethylamine (0.34 mL). The yellow mixture is heated quickly to reflux for 1 hour. The excess diamine is removed from the orange solution by a gentle stream of nitrogen. The orange mixture obtained is purified by l0 silica gel column chromatography with a gradient elution (1% methanol/chloroform (25 mL), 2% methanol/chloroform (25 mL), 4% methanol/chloroform (25 mL), 8%
methanol/chloroform (25 mL), 12% methanol/chloroform (25 mL), 16% methanol/chloroform (25 mL), 24%
methanol/chloroform (50 mL)) to yield 5-[[2-(dimethyl-amino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.010 g) as a reddish orange solid.
m.p.. 212-216°C.
~H-NMR (CDC13): 2.36 (s, 6EI); 2.69 (t, 2H); 3.54 (q, 2H);
4.21(s, 3H); 6.91 (d, 1H); 7.54 (d, lH); 8.00 (d, 1H);
8.79 (d, 1H); 9.19 (br, 1H); 9.67 (s, 1H).
Example 14 2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino]isoquino[5,6,7-cd]indazole-6(2H)-one Under a nitrogen atmosphere N,N-dimethylethylenediamine (1.79 mL) is added to a stirred solution of 2-[2-(dimethylamino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one (0.539 g) in pyridine (6.80 mL) and the resulting solution is heated at 80°C for 12 hours. The pyridine and excess N,N-dimethylethylenediamine are removed by roto-evaporation and the obtained residue is purified by silica gel column chromatography eluting first with methylene chloride, then with methylene chloride/methanol 95/5 and finally with methylene chloride/methanol/concd. ammonia from 95/5/0.5 to 95/5/1 v/v/v. The fractions containing the yellow desired product are pooled and the solvents roto-evaporated. The obtained residue (0.529 g) is crystallized from 5 diisopropylether to give 2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one as a yellow powder (0.291 g).
m.p.. 110-111°C.
'H-NMR (CDC13): 2.31 (s, 6 H); 2.38 (s, 6H); 2.71 (t, 2H);
10 2.92 (t, 2H); 3.55 (q, 2H); 4.65 (t, 2H); 7.01 (d, 1H);
7.69 (d, 1H); 8.10 (dd, 1H); 8.83 (d, 1H); 9.30 (br.t., 1H) ; 9.71 (s, 1H) .
Example 15 15 isoquino[5,6,7-cd]indazole-6(2H)-ones Using the procedures of Example 13 or 14, the following compounds are prepared by reaction of 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-chloroisoquino[5,6,7-cd]indazole-6(2H)-one, 2-[2-(dimethylamino)ethyl)-5-20 chloroisoquino[5,6,7-cd]indazole-6(2H)-one, or 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-chloroisoquino[5,6,7-cd]
indazole-6(2H)-one of Example 7:
2-[2-(N-tert-butoxycarbonylamino)ethyl)-5-[[2-(N-tert-butoxycarbonylamino)ethyl]amino] isoquino[5,6,7-25 cd]indazole-6(2H)-one;
m.p.. 211-213°C.
'H-NMR (CDC13): 1.40 (s, 9H); 1.46 (s, 9H); 3.55 (q, 2H);
3.65 (q, 2H); 3.77 (q, 2H); 4.69 (t, 2H); 5.55 (br, 2H);
7.00 (d, 1H); 7.60 (d, 1H); 7.93 (dd, 1H); 8.70 (d, 1H);
30 9.10 (br.t., 1H); 9.38 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(amino)ethyl)amino)isoquino[5,6,7-cd]indazole-6(2H)-one;
(reaction performed at 50°C in DMSO as the solvent) m.p.. 221-222°C.
35 ~H-NMR (CDC13): 1.43 (s, 9H); 3.13 (t, 2H); 3.58 (q, 2H);
3.75 (q, 2H); 3.67 (t, 2H); 5.05 (br, 1H); 7.00 (d, 1H);
. 2143853 7.65 (d, 1H); 8.05 (dd, 1H); 8.60 (d, 1H); 9.30 (br., 1H);
9.75 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-[[2-[(2 hydroxyethyl)amino]ethyl]ami no]isoquino[5,6,7 cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 1.48 (s, 9H) ; 3.25 (m, 4H) ; 3.74 (q, 2H); 3.80 (m, 4H); 4.68 (t, 2H); 7.01 (d, 1H); 7.72 (d, 1H); 8.09 (dd, 1H); 8.80 (d, 1H); 9.75 (s, 1H).
2-[2-(N-tert-butoxycarbonylamino)ethyl)]-5-[[2-(dimethyl-l0 amino)ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13): 1.44 (s, 9H); 2.31 (s, 6H); 2.75 (t, 2H);
3.68 (q, 2H); 3.75 (q, 2H); 4.68 (t, 2H); 5.10 (br.m.,H);
7.03 (d, 1H); 7.70 (d, 1H); 8.15 (dd, 1H); 8.85 (d, 1H);
9.33 (br.t., 1H); 9.71 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D) : 2. 40 (s, 6H) ; 2.95 (t, 2H) ; 3 . 23 (m, 4H); 3.82 (m, 4H); 4.70 (t, 2H); 7.05 (d, 1H); 7.70 (d, 1H); 8.13 (dd, 1H); 8.85 (d, 1H); 9.70 (s, 1H).
2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]iso-quino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13): 2.39 (s, 6H); 2.95 (t, 2H); 3.15 (t, 2H);
3.68 (q, 2H); 4.68 (t, 2H); 7.00 (d, 1H); 7.65 (d, 1H);
8.12 (dd, 1H); 8.85 (d, 1H); 9.33 (br.t., 1H); 9.72 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxyethyl) amino] ethyl]amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
(reaction performed at 52°C in DMSO as solvent) m.p.. 148-151°C.
~H-NMR (D20): 2.75 (m, 6H); 2.95 (m, 2H); 3.12 (m, 2H);
3.70 (m, 4H) ; 4.05 (m, 2H) ; 6. 10 (d, 1H) ; 6. 65 (d, 1H) ;
6.90 (d, 1H); 7.83 (s, 1H); 7.95 (d, 1H).
2143$53 2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2 . 97 (t, 2H) ; 3. 30 (m, 4H) ; 3 . 68 (t, 2H); 3.85 (t, 2H); 4.66 (t, 2H); 7.00 (d, 1H); 7.69 (d, 1H); 8.10 (dd, 1H); 8.83 (d, 1H); 9.76 (s, 1H).
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[3-(amino)propyl]amino] isoquino[5,6,7-cd]indazole-6(2H)-one;
'H-NMR (CDC13 + CD30D) : 2. 09 (m, 2H) ; 2. 57 (t, 2H) ; 3. 30 (m, 4H); 3.53 (t, 2H); 3.82 (t, 2H); 4.66 (t, 2H); 7.01 (d, 1H); 7.68 (d, 1H); 8.05 (dd, 1H); 8.80 (d, 1H); 9.68 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl] amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D) : 2.48 (s, 3H) ; 2.83 (t, 2H) ; 3.28 (m, 4H); 3.58 (t, 2H); 3.83 (t, 2H); 4.67 (t, 2H); 7.01 (d, 1H); 7.68 (d, 1H); 8.03 (dd, 1H); 8.80 (d, 1H); 9.67 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethyamino) ethyl] amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
~H-NMR (CDC13 + CD30D): 2.31(s, 6H); 2.72 (t, 2H); 3.33 (m, 4H) ; 3. 57 (t, 2H) ; 3 . 87 (t, 2H) ; 4 . 71 (t, 2H) ; 7. 00 (d, 1H); 7.71 (d, 1H); 8.09 (dd, 1H); 8.81 (d, 1H); 9.70 (s, 1H) .
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(N-tert-butoxy carbonylamino)ethyl]amino]isoquino[5,6,7-cd]indazole-6 (2H)-one;
'H-NMR (CDC13 + CD30D) : 1.41 (s, 9H) ; 3. 29 (m, 4H) ; 3.56 (t, 2H); 3.79 (t, 2H); 3.83 (t, 2H); 4.68 (t, 2H); 7.05 (d, 1H); 7.68 (d, 1H); 8.08 (dd, 1H); 8.80 (d, 1H); 9.68 (s, 1H).
Example 16 Removal of the t-butoxycarbonyl protective group Under a nitrogen atmosphere an ethanolic solution of anhydrous HC1 (5N; 0.40 mL) is dropped into a stirred suspension of 2-[2-(N-tert-butoxycarbonylamino) ethyl]-5-[[2-(N-tert-butoxycarbonylamino) ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one of Example 10 (0.104 g) in absolute ethanol (2.1 mL). Initial dissolution of the starting material followed by precipitation of a dark-red solid is observed during the addition of ethanolic HC1. This solid is redissolved with absolute ethanol and the solution is heated to 40°C for 2 h, 30'. The gradual formation of a red-amaranth precipitate is observed during the heating. After cooling to room temperature diethyl ether ( l0 mL) is added and the precipitate is collected by suction filtration under a nitrogen blanket, to give 2-[2-(amino)ethyl]-5-[[2-(amino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one trihydrochloride (0.070 g).
m.p.. 247-250°C.
~H-NMR (D20) : 3.40 (t, 2H) ; 3.70 (t, 2H) ; 3 . 95 (t, 2H) ;
4.87 (t, 2H); 7.05 (d, 1H); 7.78 (d, 1H); 8.04 (dd, 1H);
8.62 (d, 1H); 9.10 (s, 2H).
UV (HZO) : ~",ex (E~~) = 230 nm (650 cm) ; 240 nm (555 cm) ; 370 nm (244 cm); 591 nm (342 cm).
Example 17 Following the procedure of Example 16, the following compounds are prepared as the trihydrochloride salt starting from the appropriate N-tent-butoxycarbonyl derivatives of Examples 11, 12, 14, or 15:
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(amino)ethyl]
amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
~H-NMR (D20) : 3. 07 (t, 2H) ; 3 . 39 (m, 4H) ; 3 . 69 (t, 2H) ;
3.88 (t, 2H) ; 4.83 (t, 2H) ; 7. 05 (d, 1H) ; 7.70 (d, 1H) ;
8.33 (dd, 1H); 8.78 (d, 1H); 9.15 (s, 1H).
,, ,. ~ 2143853 2-[2-(amino)ethyl)]-5-[[2-[(2-hydroxyethyl)amino]ethyl]
aminoJisoquino[8,7,6-cd]indazole-6(2H)-one;
~H-NMR (DZO): 3.28 (t, 2H); 3.31 (m, 4H); 3.85 (m, 4H);
4.90 (t, 2H); 7.03 (d, 1H); 7.70 (d, 1H); 8.35 (dd, 1H);
8.72 (d, 1H); 9.77 (s, 1H).
2-[2-(amino)ethyl)]-5-[[(2-(dimethylamino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one m.p.. 224C (dec.).
'H-NMR (Dz0): 3.00 (s, 6H); 3.60 (t, 2H); 3.70 (t, 2H);
4.07 (t, 2H); 4.93 (t, 2H); 7.20 (d, 1H); 7.95 (d, 1H);
8.43 (dd, 1H); 8.77 (d, 1H); 9.43 (s, 1H).
UV (HC1 0. 1N) : ~~,ax (E~~) - 236 nm (485 ; 382 nm (205 cm) cm); 507 nm (232 cm).
2-[2-(amino)ethyl]-5-[[2[(amino)ethyl]aminoJ isoquino [5,6,7-cd]indazole-6(2H)-one m.p.. > 260C.
~H-NMR (D20) : 3 . 42 (t, 2H) ; 3.75 (t, 2H) 4.00 (t, 2H) ; ;
5.05 (t, 2H); 7.32 (d, 1H); 8.09 (d, 1H); 8.62 (d, 1H);
8.87 (d, 1H); 9.55 (s, 1H) UV (HC1 0. 1N) : ~",ax (E~~) - 245 nm (622 cm) 275 nm ;
(181 cm); 351 nm (258 cm); 472 nm (327 cm), 494 nm (353 cm).
2-[2-(amino)ethyl)]-5-[[-[(2-hydroxyethyl)amino]ethyl]
amino] isoquino[5,6,7-cd]indazole-6(2H)-one;
2-[2-(amino)ethyl)]-5-[[2-(dimethylamino)ethyl]amino]
isoquino[5,6,7-cd]indazole -6(2H)-one;
Example 18 2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]
isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate A solution of malefic acid (0.030 g) in absolute ethanol (0.4 mL) is added drop-wise into a stirred solution of 2-[2-(dimethylamino) ethyl]-5-[[2-(amino) ethylJamino]isoquino[8,7,6-cd]indazole-6(2H)-one of Example 12 (0.030 g) in absolute ethanol (1.5 ml) held at ._ 50°C. After the addition is complete the reaction mixture is maintained at 50°C for 3 minutes and then allowed to cool to room temperature. After one hour the red-amaranth crystalline material which separated is filtered, washed 5 with ethanol and dried under vacuum at 40°C to give 2-[2-(dimethylamino)ethyl]-5-[[2-(amino)ethyl]amino]isoquino [8,7,6-cd]indazole -6(2H)-one dimaleate (0.029 g).
m.p.. 175-175.5°C.
~H-NMR (DZO): 3.00 (s, 6 H); 3.40 (t, 2H); 3.80 (t, 2H);
10 3.93 (t, 2H); 4.90 (t, 2H); 6.00 (s, 4H); 7.00 (d, 1H);
7.70 (d, 1H); 7.80 (d, iH); 8.55 (d, 1H); 9.00 (s, 1H).
UV (HC1 0. 1N) : ~",ax (E~~) - 236 nm (436 cm) ; 382 nm (169 cm); 507 nm (190 cm).
Example 19 15 Following the procedure of Example 18, the following maleate salts are prepared by salification of the appropriate isoquinoindazole-6(2H)-ones with malefic acid:
2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino] isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate 20 m.p.. 189-191C.
~H-NMR (DMSO-db): 2.88 (s, 12H); 3.37 (t, 3.70 2H);
(t, 2H); 3.95 (q, 2H); 5.01 (t, 2H); 6.00 (s, 4H); 7.38 (d, 1H); 8.20 (dd, 1H); 8.85 (d, 1H); 9.20 (br.t., 1H);
9.55 (s, 1H).
25 UV (HZO) : ~,",x (E,~)- 368 nm (154 cm) ; 469 nm (206 cm) ;
490 nm (211 cm).
2-[2-(dimethylamino)ethyl)]-5-[[2-(dimethylamino)ethyl]
amino] isoquino[5,6,7-cd]indazole-6(2H)-one dimaleate m.p.. 142-146C.
30 ~H-NMR (D20) : 3.00 (s, 6H) ; 3.05(s, 6H) ; 3.60(t, 2H) ;
3.92 (t, 2H) ; 4. 08 (t, 2H) ; 5.07(t, 2H) ; 6. (s, 4H) 15 ;
7.20 (d, 1H); 7.95 (d, 1H); 8.20 (d, 1H); 8.75 (d, 1H);
9.30 (s, 1H).
UV (H20) : ~",ax (E~~) - 292 nm (108 cm) ; 352 nm (133 cm) ;
35 476 nm (215 cm) .
_2143853 2-[2-(dimethylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one dimaleate m.p.. 156-157°C.
~H-NMR (D20) : 3. 05 (s, 6H) ; 3 . 30 (m, 2H) ; 3 . 54 (t, 2H) ;
3.88 (m, 4H); 4.03 (t, 2H); 4.96 (t, 2H); 6.00 (s, 4H);
7.00 (d, 1H); 7.70 (d, 1H); 7.83 (dd, 1H); 8.57 (d, 1H);
9.05 (s, 1H) (HzD) ~ ~max (Em) - 368 nm (1057 cm) ; 491 nm (210 cm) .
Claims (24)
1. A compound according to the formula (I):
wherein R is hydrogen or hydroxy;
one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R is hydrogen;
A and B are the same or different and are selected from the group of C1-C10 alkyl or phenylalkyl; C2-C10 alkyl having one or two substituents selected from the group consisting of OR1 and NR2R3; C2-C10 alkyl interrupted by one or two oxygen atoms or by one -NR4- group, and being said C2-C10 alkyl optionally substituted by one or two hydroxy (OH) or NR2R3 groups;
R1 is selected from the group consisting of hydrogen, C1 -C6 alkyl, phenyl, phenylalkyl, -S(O2)R5, C2-C6 alkyl optionally substituted by NR2R3;
R2 and R3 may be the same or different and are selected from the group consisting of hydrogen, C1-C10 alkyl, phenylalkyk, phenyl, C2-C10 alkyl substituted with one or two hydroxy (OH) groups, or R2 and R3 taken together with the nitrogen atom to which they are attached form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains a second heteroatom;
R4 is selected from the group consisting of hydrogen, C1-C10 alkyl, C2-C10 hydroxyalkyl, C2-C10 alkyl substituted by NR2R3 phenylalkyl, phenyl;
R5 is selected from the group consisting of C1-C10 alkyl, phenylalkyl;
as free bases and their salts with pharmaceutically acceptable acids.
wherein R is hydrogen or hydroxy;
one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R is hydrogen;
A and B are the same or different and are selected from the group of C1-C10 alkyl or phenylalkyl; C2-C10 alkyl having one or two substituents selected from the group consisting of OR1 and NR2R3; C2-C10 alkyl interrupted by one or two oxygen atoms or by one -NR4- group, and being said C2-C10 alkyl optionally substituted by one or two hydroxy (OH) or NR2R3 groups;
R1 is selected from the group consisting of hydrogen, C1 -C6 alkyl, phenyl, phenylalkyl, -S(O2)R5, C2-C6 alkyl optionally substituted by NR2R3;
R2 and R3 may be the same or different and are selected from the group consisting of hydrogen, C1-C10 alkyl, phenylalkyk, phenyl, C2-C10 alkyl substituted with one or two hydroxy (OH) groups, or R2 and R3 taken together with the nitrogen atom to which they are attached form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains a second heteroatom;
R4 is selected from the group consisting of hydrogen, C1-C10 alkyl, C2-C10 hydroxyalkyl, C2-C10 alkyl substituted by NR2R3 phenylalkyl, phenyl;
R5 is selected from the group consisting of C1-C10 alkyl, phenylalkyl;
as free bases and their salts with pharmaceutically acceptable acids.
2. A compound according to claim 1 wherein said heterocyclic ring is selected from the group consisting of 1-imidazolyl, 1-pyrrolyl, 1-tetrahydropyrrolyl, 1-pyrazolyl, 4-morpholinyl, 1-piperidinyl, 1-piperazinyl, 1-(4-methyl) -piperazinyl, and 1-(4-benzyl) -piperazinyl.
3. A compound according to claim 1 wherein Y is CH and X is nitrogen.
4. A compound according to claim 1 wherein Y is nitrogen and X is CH.
5. A compound according to claim 1 wherein R is hydrogen.
6. A compound according to claim 1 wherein R is hydrogen and A and B
are independently are selected from the group consisting of -(CH2)p-NH2 wherein p is the integer 2 or 3; -(CH2)p-NR2R3 wherein p is as above defined and R2 and R3 are methyl;
-(CH2)p-NR2R3 wherein p is as above defined and R2 is hydrogen and R3 is methyl;
-(CH2)p-OH wherein p is as above defined; -(CH2)p-NH-(CH2)q-OH wherein p and q are independently an integer selected from group consisting of 2 or 3.
are independently are selected from the group consisting of -(CH2)p-NH2 wherein p is the integer 2 or 3; -(CH2)p-NR2R3 wherein p is as above defined and R2 and R3 are methyl;
-(CH2)p-NR2R3 wherein p is as above defined and R2 is hydrogen and R3 is methyl;
-(CH2)p-OH wherein p is as above defined; -(CH2)p-NH-(CH2)q-OH wherein p and q are independently an integer selected from group consisting of 2 or 3.
7. A compound of claim 1 selected from the group consisting of 2-[2-[(2-hydroxyethyl) amino] ethyl]-5-[[2-[(2-hydroxyethyl) amino] ethyl]
amino]
isoquino[8,7,6-cd] indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-aminopropyl) amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-aminoethyl) amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethylamino) ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxyethyl) amino]ethyl]amino]isoquino[5,6,7-cd)indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-aminopropyl) amino]isoquino[5,6,7-cd)indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-aminoethyl) amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethylamino) ethyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-(dimethyl-amino)ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[(3-aminopropyl)amino]-2-[2-(dimethylamino)ethyl]
isoquino[8,7,6-cd]indazole-6(2H)-one;
5-[(2-aminoethyl)amino]-[2-[2-(dimethylamino)ethyl]
isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-(dimethylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl] amino]-2-[2-(di-methylamino)ethyl]isoquino[5,6,7-cd]indazole-6(2H)-one;
5-[(3-aminopropyl)amino]-2-[2-(dimethylamino)ethyl]iso-quino [5,6,7-cd]indazole-6(2H)-one;
5-[(2-aminoethyl)amino]-[2-(dimethylamino)ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-(dimethylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-[(2-hydroxyethyl)amino]ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd] indazole-6(2H)-one;
2-[2-aminoethyl)-5-[(2-aminoethyl)amino]isoquino [8,7,6-cd] indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-(methylamino)ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-(dimethylamino)ethyl]amino]iso-quino[8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl)-5-[[2-[(2-hydroxyethyl)amino]ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6 (2H)-one;
2-[3-aminopropyl]-5-[(2-amino)ethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[[2-(methylamino)ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[[2-(dimethylamino)ethyl]amino]iso-quino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[3-amino-propyl] isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-amino-ethyl]isoquino [5,6,7-cd)indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(2-aminoethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
amino]]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)]ethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]et hyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(3-aminopropyl)amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(2-aminoethyl)amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[ (2-methylamino) ethyl]-5-[ [2-(dimethylamino) ethyl] amino] isoquino [5,6,7-cd]
indazole-6 (2H)-one;
2-methyl-5-[ [2-(dimethylamino) ethyl] amino] isoquino [8,7,6-cd] indazole-6 (2H)-one; and 2-methyl-5-[ [2-(dimethylamino) ethyl] amino] isoquino [5,6,7-cd]indazole-6 (2H)-one, as their free bases and their salts with pharmaceutically acceptable salts.
amino]
isoquino[8,7,6-cd] indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-aminopropyl) amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-aminoethyl) amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethylamino) ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-[(2-hydroxyethyl) amino]ethyl]amino]isoquino[5,6,7-cd)indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(3-aminopropyl) amino]isoquino[5,6,7-cd)indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[(2-aminoethyl) amino]isoquino[5,6,7-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(methylamino) ethyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[2-[(2-hydroxyethyl)amino]ethyl]-5-[[2-(dimethylamino) ethyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-(dimethyl-amino)ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[(3-aminopropyl)amino]-2-[2-(dimethylamino)ethyl]
isoquino[8,7,6-cd]indazole-6(2H)-one;
5-[(2-aminoethyl)amino]-[2-[2-(dimethylamino)ethyl]
isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-(dimethylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl] amino]-2-[2-(di-methylamino)ethyl]isoquino[5,6,7-cd]indazole-6(2H)-one;
5-[(3-aminopropyl)amino]-2-[2-(dimethylamino)ethyl]iso-quino [5,6,7-cd]indazole-6(2H)-one;
5-[(2-aminoethyl)amino]-[2-(dimethylamino)ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-(methylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-(dimethylamino)ethyl]amino]-2-[2-(dimethylamino) ethyl]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-[(2-hydroxyethyl)amino]ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd] indazole-6(2H)-one;
2-[2-aminoethyl)-5-[(2-aminoethyl)amino]isoquino [8,7,6-cd] indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-(methylamino)ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[2-aminoethyl]-5-[[2-(dimethylamino)ethyl]amino]iso-quino[8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl)-5-[[2-[(2-hydroxyethyl)amino]ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6 (2H)-one;
2-[3-aminopropyl]-5-[(2-amino)ethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[[2-(methylamino)ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[3-aminopropyl]-5-[[2-(dimethylamino)ethyl]amino]iso-quino [8,7,6-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[3-amino-propyl] isoquino [5,6,7-cd]indazole-6(2H)-one;
5-[[2-[(2-hydroxyethyl)amino]ethyl]amino]-2-[2-amino-ethyl]isoquino [5,6,7-cd)indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]
ethyl]amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(3-aminopropyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(2-aminoethyl)amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
amino]]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)]ethyl]-5-[[2-(dimethylamino)ethyl]
amino]isoquino [8,7,6-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-[(2-hydroxyethyl)amino]et hyl]amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(3-aminopropyl)amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[(2-aminoethyl)amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[(2-methylamino)ethyl]-5-[[2-(methylamino)ethyl]
amino]isoquino [5,6,7-cd]indazole-6(2H)-one;
2-[ (2-methylamino) ethyl]-5-[ [2-(dimethylamino) ethyl] amino] isoquino [5,6,7-cd]
indazole-6 (2H)-one;
2-methyl-5-[ [2-(dimethylamino) ethyl] amino] isoquino [8,7,6-cd] indazole-6 (2H)-one; and 2-methyl-5-[ [2-(dimethylamino) ethyl] amino] isoquino [5,6,7-cd]indazole-6 (2H)-one, as their free bases and their salts with pharmaceutically acceptable salts.
8. A pharmaceutical composition suitable for the treatment of tumors in a patient comprising a compound according to claim 1 and a pharmaceutically acceptable diluent or excipient.
9. The use of am effective anti-tumor amount of a compound according to claim 1 for treating tumors in a mammal requiring such treatment.
10. A process for the synthesis of a compound according to claim 1 wherein R is hydrogen or hydroxy; one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R is hydrogen;
A and B are the same or different and are selected from the group of C1-C10 alkyl or phenylalkyl;
C2-C10 alkyl having one or two substituents selected from the group consisting of OR1, and NR2R3; C2-C10 alkyl interrupted by one or two oxygen atoms or by one -NR4-group, and being said C2-C10 alkyl optionally substituted by one or two hydroxy (OH) or NR2R3 groups;
R1 is selected from the group consisting of hydrogen, C1-C6, alkyl, phenyl, phenylalkyl, -S(O2)R5, C2-C6 alkyl optionally substituted by NR2R3;
R2 and R3 may be the same or different and are selected from the group consisting of hydrogen, C1-C10 alkyl, phenylalkyl, phenyl, C2-C10 alkyl substituted with one or two hydroxy (OH) groups, or R2 and R3 taken together with the nitrogen atom to which they are attached form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains a second heteroatom;
R4 is selected from the group consisting of hydrogen, C1-C10 alkyl, C2-C10 hydroxyalkyl, C2-C10 alkyl substituted by NR2R3, phenylalkyl, phenyl;
R5 is selected from the group consisting of C1-C10 alkyl, C7-C10 aralkyl;
said method comprising the steps of:
a) reacting compounds of formula (III):
wherein R, X, and Y are as defined above, Z is p-toluenesulfonyloxy, fluorine or chlorine, and W is fluorine or chlorine, with the proviso that Z and W cannot simultaneously be chlorine;
with an alkyl hydrazine of formula (IV):
NH2-NH-B' (IV) where B' has the meanings as B is defined in formula (I), or B' is a group that can be converted into B by removal of protective groups for the primary or secondary amines optionally present in B', to give a compound of formula (II):
wherein X, Y, R, Z and B' are as defined above;
b) which is then reacted with a compound of formula (V):
NH2-A' (V) where A' has the same meanings as A is defined in formula (I), or A' is a group that can be converted into A by removal of protective groups for the primary or secondary amines optionally present in A', to give the compounds of formula (I'):
wherein X, Y, R, A' and B' are as defined above; and wherein A' and/or B' are different from A and/or B, compounds of formula (I') can be converted to compounds of formula (I) by removal of the protective groups for the primary and/or secondary amines optionally present in A' and B'.
A and B are the same or different and are selected from the group of C1-C10 alkyl or phenylalkyl;
C2-C10 alkyl having one or two substituents selected from the group consisting of OR1, and NR2R3; C2-C10 alkyl interrupted by one or two oxygen atoms or by one -NR4-group, and being said C2-C10 alkyl optionally substituted by one or two hydroxy (OH) or NR2R3 groups;
R1 is selected from the group consisting of hydrogen, C1-C6, alkyl, phenyl, phenylalkyl, -S(O2)R5, C2-C6 alkyl optionally substituted by NR2R3;
R2 and R3 may be the same or different and are selected from the group consisting of hydrogen, C1-C10 alkyl, phenylalkyl, phenyl, C2-C10 alkyl substituted with one or two hydroxy (OH) groups, or R2 and R3 taken together with the nitrogen atom to which they are attached form an ethyleneimine ring or a 5- or 6-member aromatic or non-aromatic heterocyclic ring which optionally contains a second heteroatom;
R4 is selected from the group consisting of hydrogen, C1-C10 alkyl, C2-C10 hydroxyalkyl, C2-C10 alkyl substituted by NR2R3, phenylalkyl, phenyl;
R5 is selected from the group consisting of C1-C10 alkyl, C7-C10 aralkyl;
said method comprising the steps of:
a) reacting compounds of formula (III):
wherein R, X, and Y are as defined above, Z is p-toluenesulfonyloxy, fluorine or chlorine, and W is fluorine or chlorine, with the proviso that Z and W cannot simultaneously be chlorine;
with an alkyl hydrazine of formula (IV):
NH2-NH-B' (IV) where B' has the meanings as B is defined in formula (I), or B' is a group that can be converted into B by removal of protective groups for the primary or secondary amines optionally present in B', to give a compound of formula (II):
wherein X, Y, R, Z and B' are as defined above;
b) which is then reacted with a compound of formula (V):
NH2-A' (V) where A' has the same meanings as A is defined in formula (I), or A' is a group that can be converted into A by removal of protective groups for the primary or secondary amines optionally present in A', to give the compounds of formula (I'):
wherein X, Y, R, A' and B' are as defined above; and wherein A' and/or B' are different from A and/or B, compounds of formula (I') can be converted to compounds of formula (I) by removal of the protective groups for the primary and/or secondary amines optionally present in A' and B'.
11. A method for the synthesis of a compound of formula (III'):
wherein R6 is hydrogen or a suitable protective group of a hydroxy group; one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R6 is hydrogen; OTs is p-toluenesulfonyloxy; and W is fluorine or chlorine, said method comprising the following steps:
(a) the Friedel and Craft acylation of 1,4-difluorobenzene, in the presence of AlCl3, with a pyridine-3, 4-dicarboxylic anhydride of formula (VI):
wherein R6 is as defined above, which leads to regioisomeric keto-acids of formulae (VIIa) and (VIIb):
wherein R6 is as defined above;
(b) reaction of the ketoacids of formulae (VIIa) and (VIIb) as defined above, with sodium methoxide in methanol leading to regioisomeric methoxy-substituted ketoacids of formulae (VIIIa) and (VIIIb):
wherein R6 is as defined above, and when R6 is hydrogen, compounds of formulae (VIIIa) and (VIIIb) can be reacted as such in step (c), and when R6 is different from hydrogen, the compound of formula (VIIIa) is purified by crystallization and reacted as pure regioisomer;
(c) reduction of compounds of formulae (VIIIa) and (VIIIb), as defined above, with Zn/Cu couple in formic acid leading to compounds of formulae (IXa) and (IXb):
wherein R6 is as defined above, and when R6 is hydrogen, the acids of formulae (IXa) and (IXb) can be separated by chromatography yielding the pure isolated regioisomers of formulae (IXa) and (IXb);
(d) cyclization of the acids of formulae (IXa) and (IXb) as defined above, by heating a suspension of the compounds of formulae (IXa) and (IXb) in polyphosphoric acid leading to a benzo[g]isoquinoline of formula (X):
wherein X, Y and R6 are as defined above;
(e) oxidation of the compound of formula (X) as defined above, by cerium ammonium nitrate in a mixture of acetonitrile and water to the corresponding dione of formula (XI):
wherein X, Y and R6 are as defined above;
(f) removal of the methoxy group of the dione of formula (XI) as defined above, by aluminum chloride in methylene chloride leading to compounds of formula (XIIa) and (XIIb):
(XII) (XIIa) W = F
(XIIb) W = Cl wherein X, Y, R6 and W are as defined above, and which corresponds to a mixture of a 9-fluoro-6-hydroxy-5,10-dione of formula (XIIa) and a 9-chloro-6-hydroxy-5,10-dione of formula (XIIb) due to partial substitution of the leaving fluoride by means of AlCl3;
(g) the conversion of the free hydroxy group in a compound of formula (XII) as defined above, to the p-toluenesulfonyloxy group (OTs), by means of toluenesulfonyl chloride in pyridine, leading to the compound of formula (III') as defined above.
wherein R6 is hydrogen or a suitable protective group of a hydroxy group; one of X and Y is CH and the other is a nitrogen atom, with the proviso that when Y is nitrogen, R6 is hydrogen; OTs is p-toluenesulfonyloxy; and W is fluorine or chlorine, said method comprising the following steps:
(a) the Friedel and Craft acylation of 1,4-difluorobenzene, in the presence of AlCl3, with a pyridine-3, 4-dicarboxylic anhydride of formula (VI):
wherein R6 is as defined above, which leads to regioisomeric keto-acids of formulae (VIIa) and (VIIb):
wherein R6 is as defined above;
(b) reaction of the ketoacids of formulae (VIIa) and (VIIb) as defined above, with sodium methoxide in methanol leading to regioisomeric methoxy-substituted ketoacids of formulae (VIIIa) and (VIIIb):
wherein R6 is as defined above, and when R6 is hydrogen, compounds of formulae (VIIIa) and (VIIIb) can be reacted as such in step (c), and when R6 is different from hydrogen, the compound of formula (VIIIa) is purified by crystallization and reacted as pure regioisomer;
(c) reduction of compounds of formulae (VIIIa) and (VIIIb), as defined above, with Zn/Cu couple in formic acid leading to compounds of formulae (IXa) and (IXb):
wherein R6 is as defined above, and when R6 is hydrogen, the acids of formulae (IXa) and (IXb) can be separated by chromatography yielding the pure isolated regioisomers of formulae (IXa) and (IXb);
(d) cyclization of the acids of formulae (IXa) and (IXb) as defined above, by heating a suspension of the compounds of formulae (IXa) and (IXb) in polyphosphoric acid leading to a benzo[g]isoquinoline of formula (X):
wherein X, Y and R6 are as defined above;
(e) oxidation of the compound of formula (X) as defined above, by cerium ammonium nitrate in a mixture of acetonitrile and water to the corresponding dione of formula (XI):
wherein X, Y and R6 are as defined above;
(f) removal of the methoxy group of the dione of formula (XI) as defined above, by aluminum chloride in methylene chloride leading to compounds of formula (XIIa) and (XIIb):
(XII) (XIIa) W = F
(XIIb) W = Cl wherein X, Y, R6 and W are as defined above, and which corresponds to a mixture of a 9-fluoro-6-hydroxy-5,10-dione of formula (XIIa) and a 9-chloro-6-hydroxy-5,10-dione of formula (XIIb) due to partial substitution of the leaving fluoride by means of AlCl3;
(g) the conversion of the free hydroxy group in a compound of formula (XII) as defined above, to the p-toluenesulfonyloxy group (OTs), by means of toluenesulfonyl chloride in pyridine, leading to the compound of formula (III') as defined above.
12. A method for the preparation of compounds of formula (III"):
wherein R6 is hydrogen or a suitable protective group of a hydroxy group, said method comprising the following steps:
a) lithiation of 1-chloro-4-fluorobenzene with an alkyllithium reagent to give 1-lithio-5-chloro-2-fluorobenzene of formula (XIV):
b) acylation of 1-lithio-5-chloro-2-fluorobenzene of formula (XIV) as defined above, with a pyridine-3,4-dicarboxylic anhydride of formula (VI):
wherein R6 is as defined above, to give a mixture of keto-acids of formulae (XVa) and (XVb):
wherein R6 is as defined above, and which can be separated into the pure compounds of formulae (XVa) and (XVb) by recrystallization from a solvent or by sublimation;
c) reduction of the pure keto-acid of formula (XVa) as defined above, with Zn/Cu couple or Zn powder, in formic acid leading to a compound of formula (XVI):
wherein R6 is as defined as above; and d) oxidative cyclization of a compound of formula (XVI) as defined above, with fuming sulfuric acid to give the 9-chloro-6-fluorobenzo[g]
isoquinoline-5,10-dione of formula (III") as defined above.
wherein R6 is hydrogen or a suitable protective group of a hydroxy group, said method comprising the following steps:
a) lithiation of 1-chloro-4-fluorobenzene with an alkyllithium reagent to give 1-lithio-5-chloro-2-fluorobenzene of formula (XIV):
b) acylation of 1-lithio-5-chloro-2-fluorobenzene of formula (XIV) as defined above, with a pyridine-3,4-dicarboxylic anhydride of formula (VI):
wherein R6 is as defined above, to give a mixture of keto-acids of formulae (XVa) and (XVb):
wherein R6 is as defined above, and which can be separated into the pure compounds of formulae (XVa) and (XVb) by recrystallization from a solvent or by sublimation;
c) reduction of the pure keto-acid of formula (XVa) as defined above, with Zn/Cu couple or Zn powder, in formic acid leading to a compound of formula (XVI):
wherein R6 is as defined as above; and d) oxidative cyclization of a compound of formula (XVI) as defined above, with fuming sulfuric acid to give the 9-chloro-6-fluorobenzo[g]
isoquinoline-5,10-dione of formula (III") as defined above.
13. A compound according to claim 1 wherein the second heteroatom is selected from the group consisting of sulfur, oxygen and nitrogen.
14. A process, according to claim 10 wherein the second heteroatom is selected from the group consisting of sulfur, oxygen and nitrogen.
15. A pharmaceutical composition according to claim 8 wherein the tumors are susceptible to azaanthrapyrazole treatment.
16. The use according to claim 9, wherein the tumors are susceptible to azaanthrapyrazole treatment.
17. A method for the synthesis of compounds of formula (III') according to claim 11, wherein R6 is a suitable protective group of the hydroxy function selected from the group consisting of methoxy and benzyloxy.
18. A method for the synthesis of a compound of formula (III') according to claim 11, wherein R6 is a protective group of the hydroxy group in the compound of formula (III'), the protective group of R6 can be removed to give a compound of formula (III) according to claim 10, where R is OH in formula (III).
19. A method for the preparation of compounds of formula (III") according to claim 12, wherein 1-chloro-4-fluorobenzene is lithiated with an alkyllithium reagent in THF at -75°C
20. A method for the preparation of compounds of formula (III") according to claim 12 or claim 19, wherein 1-chloro-4-fluorobenzene is lithiated with sec-butyllithium.
21. A method for the preparation of compounds of formula (III") according to claim 12, wherein 1-lithio-5-chloro-2-fluorobenzene is generated in situ according to step (a) of claim 12, and reacted as such in step (b) of claim 12.
22. A method for the preparation of compounds of formula (III") according to claim 12, wherein the pure keto acid of formula (XVa) is reduced with Zn/Cu couple or Zn powder, in 75% aqueous formic acid for 15 min. at room temperature, then for 2 hrs at 80°C.
23. A method for the preparation of compounds of formula (III") according to claim 12, wherein the compound of formula (XVI) is oxidatively cyclized with fuming sulfuric acid, 20-30% SO3, for 10 min. at 130°C.
24. A method for the synthesis of a compound of formula (III") according to claim 12, wherein R6 is a protective group of the hydroxy group in the compound of formula (III"), the protective group of R6 can be removed to give a compound of formula (III) according to claim 10, where R is OH in formula (III).
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94160792A | 1992-09-08 | 1992-09-08 | |
| US07/941,607 | 1992-09-08 | ||
| US08/103,641 | 1993-08-11 | ||
| US08/103,641 US5519029A (en) | 1992-09-08 | 1993-08-11 | 2-aminoalkyl-5-aminoalkylamino substituted-isoquinoindazole-6(2H)-ones |
| PCT/US1993/008241 WO1994006795A1 (en) | 1992-09-08 | 1993-09-08 | 2-aminoalkyl-5-aminoalkylamino substituted isoquinoindazole-6-(2h)-ones with antitumour activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2143853A1 CA2143853A1 (en) | 1994-03-09 |
| CA2143853C true CA2143853C (en) | 2006-02-07 |
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ID=35890172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002143853A Expired - Lifetime CA2143853C (en) | 1992-09-08 | 1993-09-08 | 2-aminoalkyl-5-aminoalkylamino substituted isoquinoindazole-6-(2h)-ones with antitumour activity |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2143853C (en) |
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1993
- 1993-09-08 CA CA002143853A patent/CA2143853C/en not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| CA2143853A1 (en) | 1994-03-09 |
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