Naphthalene derivatives and composition and methods of use, and aldehyde intermediates

This invention relates to naphthalene derivatives useful as hypolipidemic agents.
Hyperlipidemia such as hypercholesterolemia has been known to be a major risk factor for arteriosclerosis including atherosclerosis, and drugs such as clofibrate [chemical name: 2-(4-chlorophenoxy)-2-methylpropanoic acid ethyl ester], probucol [chemical name: 4,4'-[(1-methylethylidene)bis(thio)]bis[2,6-bis(1,1-dimethylethyl)-phenol]] and cholestyramine resin have been used as hypolipidemic agents.
It is known that cholesterol in blood serum exists in various forms such as very-low-density lipoprotein (VLDL) cholesterol, low-density lipoprotein (LDL) cholesterol and high-density lipoprotein (HDL) cholesterol. In this connection, it is also known that HDL has therapeutic or prophylactic effect for arteriosclerosis because of its preventing effect on deposition of cholesterol on the arterial wall, while VLDL and LDL induce the deposition of cholesterol and are causative of arteriosclerosis [Annals of Internal Medicine, vol. 90, page 85-91 (1979)].
Therefore, in the field of therapy or prophylaxis of arteriosclerosis, it has been desired to develop a hypolipidemic agent which can decrease the serum total cholesterol level and at the same time can increase the serum HDL-cholesterol level.
On the other hand, Journal of the Chemical Society (Chemical Communications), page 354 (1980), discloses 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene and 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid lactone. Further, Chemical Abstracts, vol. 53, 20025i (1959) discloses 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-dimethoxy-2-naphthoic acid lactone and 1-(3,4-dimethoxyphenyl)-2-ethoxycarbonyl-4-hydroxy-6,7-dimethoxynaphthalene. However, no therapeutic effect of these compounds has been known up to now.
As a result of various investigations, we have now found that a naphthalene derivative of the formula: ##STR3## wherein R.sup.1 is hydrogen atom or a lower alkoxycarbonyl and R.sup.2 is a lower alkoxycarbonyl, or R.sup.1 and R.sup.2 are combined together to form a group of the formula: ##STR4## each of R.sup.3 and R.sup.4 is a lower alkoxy, or one of R.sup.3 and R.sup.4 is hydrogen atom and the other is a lower alkoxy; and
Ring A is a substituted or unsubstituted benzene ring;
and a pharmaceutically acceptable salt thereof are useful as a hypolipidemic agent.
Thus, an object of the present invention is to provide a naphthalene derivative (I) which is useful for therapeutic treatment or prophylaxis of hyperlipidemia and/or arteriosclerosis. Another object is to provide a novel pharmaceutical composition for use as a hypolipidemic agent, which comprises the naphthalene derivative (I) as the therapeutically active ingredient. The other object is to provide a novel naphthalene derivative useful as a hypolipidemic agent. And still other object is to provide processes for preparing said novel naphthalene derivative.
The naphthalene derivative (I) or a pharmaceutically acceptable salt thereof shows a potent hypolipidemic activity and is particularly characterized in that it can increase the serum HDL-cholesterol level while decreasing the serum total cholesterol level. For example, when the effect of a test compound (dose: 20 mg % in diet) on the serum total cholesterol level and the serum HDL-cholesterol level was examined by feeding rats with a diet supplimented with cholesterol and sodium cholate, 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene of the present invention showed 52% decrease in serum total cholesterol level and 86% increase in the serum HDL-cholesterol level.
Moreover, the naphthalene derivative (I) and a pharmaceutically acceptable salt thereof are low in toxicity and substantially free from undesirable side effects such as hepatic dysfunction. For example, when 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene was administered orally to mice at a dose of 1000 mg/kg, no mice died even 5 days after the oral administration.
Representative examples of the naphthalene derivative of the present invention include those of the formula (I) in which R.sup.1 is hydrogen atom or a lower alkoxycarbonyl (e.g., methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl) and R.sup.2 is a lower alkoxycarbonyl (e.g., methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl); or R.sup.1 and R.sup.2 are combined together to form a group of the formula: ##STR5## each of R.sup.3 and R.sup.4 is a lower alkoxy (e.g., methoxy, ethoxy, propoxy, isopropoxy, butoxy), or one of R.sup.3 and R.sup.4 is hydrogen atom and the other is a lower alkoxy (e.g., methoxy, ethoxy, propoxy, isopropoxy, butoxy); and Ring A is an unsubstituted benzene ring, a benzene ring having a substituent of a lower alkylenedioxy (e.g., methylenedioxy, ethylenedioxy) or a benzene ring having one to 3 substituent(s) selected from the group consisting of a lower alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl), a lower alkoxy (e.g., methoxy, ethoxy, propoxy, isopropoxy, butoxy), a phenyl-lower alkoxy (e.g., benzyloxy, phenethyloxy), hydroxy and halogen atom (e.g., fluorine atom, chlorine atom, bromine atom, iodine atom).
Among these derivatives, preferred examples include those of the formula (I) in which R.sup.1 is hydrogen atom or a lower alkoxycarbonyl and R.sup.2 is a lower alkoxycarbonyl, or R.sup.1 and R.sup.2 are combined together to form a group of the formula: ##STR6## each of R.sup.3 and R.sup.4 is a lower alkoxy, or one of R.sup.3 and R.sup.4 is hydrogen atom and the other is a lower alkoxy, and Ring A is a benzene ring of the formula: ##STR7## wherein R.sup.a is hydrogen atom, a lower alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl) or a lower alkoxy (e.g., methoxy, ethoxy, propoxy, isopropoxy, butoxy), R.sup.b is a lower alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl), R.sup.c is hydrogen atom, a lower alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl) or a phenyl-lower alkyl (e.g., benzyl, phenethyl), each of R.sup.d, R.sup.e and R.sup.f is a lower alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl) and each of X.sup.a and X.sup.b is halogen atom (e.g., fluorine atom, chlorine atom, bromine atom, iodine atom).
Another preferred examples of the naphthalene derivative (I) include
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene,
1-(3,4-dimethoxyphenyl)-2-methoxycarbonyl-3-ethoxycarbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene,
1-(3,4-dimethoxyphenyl)-2-ethoxycarbonyl-3-methoxycarbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene,
1-(3,4-dimethoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene,
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene,
1-(3,4-diethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene,
1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid lactone,
1-(3,4-diethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,76,7-methylenedioxy-2-naphthoic acid lactone,
1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-7,8-dichloro-2-naphthoic acid lactone,
1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-7-methyl-2-naphthoic acid lactone,
1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-7,8-methylenedioxy-2-naphthoic acid lactone, and the like.
The naphthalene derivative (I) may be used for the purpose of the present invention either in the free form or in the form of a pharmaceutically acceptable salt. Examples of the pharmaceutically acceptable salt of the naphthalene derivative (I) include alkali metal salts (e.g., sodium salt, potassium salt), alkaline earth metal salts (e.g., calcium salt), quarternary ammonium salts (e.g., tetramethylammonium salt, tetraethylammonium salt) and so forth.
The daily dose of the naphthalene derivative (I) or a pharmaceutically acceptable salt thereof may vary over a wide range depending on the severity of the diseases; the ages, weight and condition of patient and the like, but the preferred daily dose may be usually in the range of 1.5 to 35 mg, especially 5 to 25 mg, per kg of body weight.
The naphthalene derivative (I) or a pharmaceutically acceptable salt thereof may be administered either orally or parenterally to warm-blooded animals including human beings, while it is generally preferred to administer it through oral route. The naphthalene derivative (I) or a salt thereof may be used in the form of pharmaceutical composition in admixture with a pharmaceutically acceptable adjuvant or carrier therefor. For example, the pharmaceutical composition for oral administration may be in a solid dosage form such as tablets, pills, powders, capsules or granules; and it may contain a pharmaceutically acceptable adjuvant or carrier such as calcium carbonate, calcium phosphate, corn starch, potato starch, sugar, lactose, talcum, magnesium stearate and the like. Said pharmaceutical composition in a solid form may further contain binders, diluents, disintegrants, wetting agents and so forth. Alternatively, the pharmaceutical composition for oral administration may be in a liquid dosage form such as aqueous or oily suspensions, solutions, syrup, elixirs and the like. Suitable adjuvants for such liquid dosage form may include liquid vehicles, suspending agents, surfactants, non-liquid vehicles and so forth. On the other hand, the pharmaceutical composition for parenteral administration may be in the form of injections or suppositories. The injections may be either a solution or a suspension, which may contain a pharmaceutically acceptable carrier such as essential oil (e.g., peanut oil, corn oil) or aprotic solvent (e.g., polyethyleneglycol, polypropyleneglycol, lanolin, coconut oil).
As mentioned hereinbefore, the naphthalene derivative (I) and a pharmaceutically acceptable salt thereof have a potent hypolipidemic activity. Especially, the naphthalene derivative (I) and a salt thereof are characterized in that they can decrease serum total cholesterol level and at the same time can increase the serum HDL-cholesterol level in blood. Therefore, the naphthalene derivative (I) and a salt thereof are useful for the treatment or prophylaxis of hyperlipidemia (e.g., hypercholesterolemia) or arteriosclerosis (e.g., atherosclerosis, Munkeberg's sclerosis, arteriolosclerosis) in warm-blooded animals including human beings.
Among the naphthalene derivative (I) of the present invention, a compound of the following formula (I-a) is a novel compound. ##STR8## wherein R.sup.11 is hydrogen atom or a lower alkoxycarbonyl and R.sup.21 is a lower alkoxycarbonyl, or R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR9## each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy; and
Ring B is a substituted or unsubstituted benzene ring,
with the provisos that
(a) if both of R.sup.11 and R.sup.21 are methoxycarbonyl and Ring B is a benzene ring of the formula: ##STR10## or (b) if R.sup.11 is hydrogen atom, R.sup.21 is ethoxycarbonyl and Ring B is a benzene ring of the formula: ##STR11## or (c) if R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR12## and Ring B is a benzene ring of the formula: ##STR13## each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy.
Representative examples of the above-mentioned Ring B include an unsubstituted benzene ring, a benzene ring having a substituent of a lower alkylenedioxy and a benzene ring having one to 3 substituent(s) selected from the group consisting of a lower alkyl, a lower alkoxy, a phenyl-lower alkoxy, hydroxy and halogen atom.
Preferred examples of the compound (I-a) include those of the formula (I-a) in which
(A) each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, and
(a) each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is an unsubstituted benzene ring, a benzene ring of the formula: ##STR14## or a benzene ring having one to 3 substituent(s) selected from the group consisting of a lower alkyl, a lower alkoxy, a phenyl-lower alkoxy, hydroxy and halogen atom; or
(b) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR15## or (B) R.sup.11 is hydrogen atom, R.sup.21 is a lower alkoxycarbonyl, and
(a) each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is an unsubstituted benzene ring, a benzene ring having a substituent of a lower alkylenedioxy, a benzene ring having one or 3 substituent(s) of a lower alkoxy, a benzene ring having one to 3 substituent(s) selected from the group consisting of a lower alkyl and halogen atom, or a benzene ring of the formula: ##STR16## wherein R.sup.g is hydrogen atom or a phenyl-lower alkyl, and R.sup.b is the same as defined above; or
(b) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring having 2 substituents of a lower alkoxy; or
(C) R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR17## and (a) each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is an unsubstituted benzene ring, a benzene ring having one or 3 substituent(s) of a lower alkoxy, a benzene ring having one to 3 substituent(s) selected from the group consisting of a lower alkyl and halogen atom, or a benzene ring of the formula: ##STR18## wherein R.sup.b and R.sup.g are the same as defined above; or (b) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR19## wherein R.sup.h is a lower alkyl and R.sup.b is the same as defined above.
Another preferred examples of the compound (I-a) include those of the formula (I-a) in which
(A) each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, and
(a) each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR20## wherein R.sup.a, R.sup.b, R.sup.c, R.sup.d, R.sup.e, R.sup.f, X.sup.a and X.sup.b are the same as defined above; or
(b) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR21## or (B) R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR22## and (a) each of R.sup.31 and R.sup.41 is a lower alkoxy, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR23## wherein R.sup.a, R.sup.b, R.sup.d, R.sup.e, R.sup.f, R.sup.g, X.sup.a and X.sup.b are the same as defined above; or
(b) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR24## wherein R.sup.b and R.sup.h are the same as defined above.
Stil another preferred examples include those of the formula (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, or R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR25## and (A) each of R.sup.31 and R.sup.41 is a lower alkoxy and Ring B is a benzene ring of the formula: ##STR26## or (B) each of R.sup.31 and R.sup.41 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.31 and R.sup.41 is hydrogen atom and the other is methoxy, and Ring B is a benzene ring of the formula: ##STR27##
Other preferred examples of the compound (I-a) include those of the formula (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, or R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR28## each of R.sup.31 and R.sup.41 is a lower alkoxy and Ring B is a benzene ring of the formula: ##STR29##
Still other preferred examples include those of the formula (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, each of R.sup.31 and R.sup.41 is a lower alkoxy and Ring B is a benzene ring of the formula: ##STR30## wherein R.sup.d, R.sup.e and R.sup.f are the same as defined above.
Further preferred examples include those of the compound (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl or R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR31## both of R.sup.31 and R.sup.41 are methoxy and Ring B is a benzene ring of the formula: ##STR32##
Still further preferred examples include those of the compound (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl or R.sup.11 and R.sup.21 are combined together to form a group of the formula: ##STR33## both of R.sup.31 and R.sup.41 are methoxy and Ring B is a benzene ring of the formula: ##STR34##
Among them, the compound of the formula: (I-a) in which each of R.sup.11 and R.sup.21 is a lower alkoxycarbonyl, each of R.sup.31 and R.sup.41 is a lower alkoxy, and Ring B is a benzene ring of the formula: ##STR35## is most preferred.
Among the above-mentioned compound (I-a) of the present invention, a compound of the formula: ##STR36## wherein R.sup.12 is hydrogen atom or a lower alkoxycarbonyl, R.sup.5 is a lower alkyl, and R.sup.31, R.sup.41 and Ring B are the same as defined above, can be prepared by condensing a compound of the formula:
R.sup.12 --C.tbd.C--COOR.sup.5 (II)
wherein R.sup.12 and R.sup.5 are the same as defined above, with an aldehyde compound of the formula: ##STR37## wherein R.sup.31, R.sup.41 and Ring B are the same as defined above, or its di-lower alkyl acetal or a salt thereof.
Alternatively, a compound of the formula: ##STR38## wherein Ring C is a benzene ring of the formula: ##STR39## and R.sup.12, R.sup.31, R.sup.41, R.sup.5, X.sup.a and X.sup.b are the same as define above, may also be prepared by condensing the compound (II) with a compound of the formula: ##STR40## wherein R.sup.6 is a branched alkyl or a cycloalkyl, R.sup.7 is hydrogen atom or a lower alkyl, and R.sup.31, R.sup.41 and Ring C are the same as defined above, or a salt thereof.
On the other hand, among the compound (I-a), a compound of the formula: ##STR41## wherein each of R.sup.32 and R.sup.42 is a lower alkoxy, or one of R.sup.32 and R.sup.42 is hydrogen atom and the other is a lower alkoxy,
Ring D is a substituted or unsubstituted benzene ring, and R.sup.5 is the same as defined above, with the proviso that
if R.sup.5 is ethyl and Ring D is a benzene ring of the formula: ##STR42## each of R.sup.32 and R.sup.42 is a lower alkoxy of at least 2 carbon atoms, or one of R.sup.32 and R.sup.42 is hydrogen atom and the other is a lower alkoxy, may be prepared by treating a compound of the formula: ##STR43## wherein each of R.sup.8 and R.sup.9 is a lower alkyl, and R.sup.32, R.sup.42 and Ring D are the same as defined above, or a salt thereof, with an alkali agent to give a compound of the formula: ##STR44## wherein R.sup.32, R.sup.42 and Ring D are the same as defined above, followed by esterification thereof.
Moreover, among the compound (I-a), a compound of the formula: ##STR45## wherein each of R.sup.33 and R.sup.43 is a lower alkoxy, or one of
R.sup.33 and R.sup.43 is hydrogen atom and the other is a lower alkoxy, and
Ring E is a substituted or unsubstituted benzene ring with the proviso that
if Ring E is a benzene ring of the formula: ##STR46## each of R.sup.33 and R.sup.43 is a lower alkoxy of at least 2 carbon atoms or one of R.sup.33 and R.sup.43 is hydrogen atom and the other is a lower alkoxy,
is prepared by reductive lactonization of a compound of the formula: ##STR47## wherein R.sup.33, R.sup.43, R.sup.8, R.sup.9 and Ring E are the same as defined above, or a salt thereof.
The condensation reaction of the compound (II) with the aldehyde compound (III) or its di-lower alkyl acetal or a salt thereof and the condensation reaction of the compound (II) with the compound (IV) or a salt thereof may be accomplished in the presence of an acid in or without a solvent. Examples of the di-lower alkyl acetal of the compound (III) include dimethyl acetal, diethyl acetal, dipropyl acetal, dibutyl acetal and the like. On the other hand, examples of the compound (IV) include those of the formula (IV) in which R.sup.6 is cyclopentyl, cyclohexyl, cycloheptyl, isopropyl, sec-butyl or tert-butyl and R.sup.7 is hydrogen atom, methyl, ethyl, propyl or butyl. The salt of the aldehyde compound (III) or its di-lower alkyl acetal includes alkali metal salts (e.g., potassium salt, sodium salt) and alkaline earth metal salts (e.g., calcium salt). On the other hand, the salt of the compound (IV) includes inorganic acid addition salts (e.g., hydrochloride) and organic acid addition salts (e.g., p-toluenesulfonate, methanesulfonate). The acid which is used in this reaction includes, for example, inorganic acids such as hydrochloric acid or sulfuric acid; and organic acids such as formic acid, acetic acid, p-toluenesulfonic acid or methanesulfonic acid. Benzene, toluene, xylene or dimethylformamide is suitable as the solvent. It is preferred to carry out the reaction at a temperature between 0.degree. to 150.degree. C., especially at 50.degree. to 100.degree. C.
The aldehyde compound (III) to be used in the above-mentioned reaction is in equilibrium with the compound (III') as shown in the following scheme. ##STR48## wherein R.sup.31, R.sup.41 and Ring B are the same as defined above. Therefore, the compound (III) encompasses within the scope thereof the compound (III') and a mixture of the compounds (III) and (III').
Concomitantly, when in the thus-obtained product (I-b) or (I-c) the lowr alkoxycarbonyl group shown by R.sup.12 is identical with the lower alkoxycarbonyl group shown by the group: -COOR.sup.5, said product may be, if required, converted into the compound (I-b) or (I-c) in which said lower alkoxycarbonyl groups are different from each other by reacting the former compound with a lower alkanol of the formula: R.sup.1a --OH (wherein R.sup.1a is a lower alkyl other than R.sup.5). Examples of the lower alkanol include methanol, ethanol, propanol and butanol. It is preferred to carry out the reaction in the presence of an alkali metal such as sodium or potassium. It is also preferred to carry it out at a temperature between 0.degree. C. and a refluxing temperature.
The conversion of the compound (V) or a salt thereof (e.g., alkali metal salts, alkaline earth metal salts, quarternary ammonium salts) into the compound (VI) may be accomplished by treating the compound (V) or a salt thereof with an alkali agent in a solvent. Examples of the compound (V) include those of the formula (V) in which each of R.sup.8 and R.sup.9 is methyl, ethyl, propyl or butyl. The alkali agent which is used in the reaction includes, for example, inorganic bases such as potassium hydroxide or sodium hydroxide. Aqueous alkanols such as aqueous methanol, aqueous ethanol, aqueous propanol or aqueous butanol are suitable as the solvent. It is preferred to carry out the reaction at a temperature between 0.degree. C. and a refluxing temperature.
The subsequent esterification of the thus-obtained compound (VI) may be accomplished by reacting said compound with a lower alkanol. Examples of the lower alkanol include methanol, ethanol, propanol and butanol. When an excess amount of the lower alkanol is used, it is not always necessary to use a solvent because said lower alkanol serves as the solvent. A mixture of the above-mentioned lower alkanol and dioxane may also be used as the solvent. It is preferred to carry out the reaction in the presence of thionyl chloride or hydrogen chloride. It is also preferred to carry it out at a temperature between -10.degree. and 80.degree. C., especially at 0.degree. to 40.degree. C.
The reductive lactonization of the compound (VII) or a salt thereof (e.g., alkali metal salts, alkaline earth metal salts, quarternary ammonium salts) may be accomplished by a conventional method, for example, by treating said compound with a reducing agent in a solvent (e.g., tetrahydrofuran, ethyl ether, dimethoxyethane) at a temperature between 0.degree. C. and a refluxing temperature and then treating the product with a catalytic amount of acid. The reducing agent includes, for example, borane-complexes (e.g., borane-methylsulfide complex, borane-tetrahydrofuran complex, borane-pyridine complex), sodium borohydride-boron trifluoride etherate complex, calcium borohydride, lithium borohydride and lithium aluminum hydride. On the other hand, the acid includes, for example, inorganic acids such as hydrochloric acid and sulfuric acid; and organic acids such as formic acid, acetic acid and methanesulfonic acid.
Concomitantly, when the thus-obtained product (I-b), (I-d) or (I-e) has at least one phenyl-lower alkoxy on Ring B, D or E thereof, said phenyl-lower alkoxy may be, if required, converted into hydroxy by catalytic hydrogenation. Said catalytic hydrogenation may be carried out in the presence of a catalyst (e.g., palladium-charcoal) at 10.degree. to 50.degree. C. in hydrogen atmosphere.
The naphthalene compound (I) of the present invention other than those of the formula (I-a) may be prepared according to either one of the methods described in Journal of the Chemical Society (Chemical Communications), page 354 (1980) and Chemical Abstracts, vol. 53, 20025i (1959) or the methods used for preparation of the compound (I-a).
A pharmaceutically acceptable salt of the naphthalene derivative (I) of the present invention may be readily obtained. For example, such salt may be prepared by treating the naphthalene derivative (I) with an alkali agent such as alkali metal hydroxide (e.g., sodium hydroxide, potassium hydroxide), an alkaline earth metal hydroxide (e.g., calcium hydroxide), a quarternary ammonium hydroxide (e.g., tetramethylammonium hydroxide, tetraethylammonium hydroxide) and the like in a solvent.
Among the starting compounds mentioned above, the di-lower alkyl acetal of the compound (III) may be prepared, for example, by reacting an aldehyde compound of the formula: ##STR49## wherein R.sup.31 and R.sup.41 are the same as defined above, with an acetal compound of the formula: ##STR50## wherein R.sup.10 is a lower alkyl and Ring B is the same as defined above. The thus-obtained di-lower alkyl acetal of the compound (III) may be, if required, converted into the aldehyde compound (III) by treating the former compound with an acid.
Alternatively, the aldehyde compound (III) in which Ring B is a benzene ring of the formula: ##STR51## wherein R.sup.d, R.sup.e and R.sup.f are the same as defined above, may be prepared, for example, by reacting the compound (VIII) with a compound of the formula: ##STR52## wherein Ring F is a benzene ring of the formula: ##STR53## and R.sup.6, R.sup.d, R.sup.e and R.sup.f are the same as defined above.
Moreover, the starting compound (IV) may be prepared, for example, by reacting the compound (VIII) with a compound of the formula: ##STR54## wherein R.sup.6 and Ring C are the same as defined above, and if required, further reacting the resultant product of the formula: ##STR55## wherein R.sup.31, R.sup.41, R.sup.6 and Ring C are the same as defined above, with a lower alkyl halide.
The reaction of the compound (VIII) with the compound (IX), (X) or (XI) may be carried out in the presence of an alkyl lithium in a solvent at a temperature between -100.degree. C. and a refluxing temperature. The conversion of the di-lower alkyl acetal of the compound (III) into the free aldehyde compound (III) may be carried out by treating said di-lower alkyl acetal with an acid (e.g., hydrochloric acid, trifluoroacetic acid) in a solvent (e.g., aqueous methanol, aqueous ethanol) at 0.degree. to 30.degree. C. Further, the reaction of the compound (XII) with the lower alkyl halide may be carried out in the presence of an acid acceptor in a solvent at a temperature between -10.degree. and 100.degree. C.
Practical and presently-preferred embodiments of the present invention are illustratively shown in the following Experiments and Examples.
Throughout the Specification and Claims, the terms "lower alkyl", "lower alkoxy", "lower alkoxycarbonyl" and "lower alkylenedioxy" should be interpreted as referring to alkyl of one to 4 carbon atoms, alkoxy of one to 4 carbon atoms, alkoxycarbonyl of 2 to 5 carbon atoms and alkylenedioxy of one or 2 carbon atoms, respectively. Further, when R.sup.1 (or R.sup.11) and R.sup.2 (or R.sup.21) are combined together to form a group of the formula: ##STR56## it should be interpreted that said R.sup.1 (or R.sup.11) and R.sup.2 (or R.sup.21) taken together with adjacent naphthol ring form 9-hydroxynaphtho[2,3-c]furan-3(1H)-one ring of the formula: ##STR57##
Experiment
Effect on serum total chloesterol level and serum HDL-cholesterol level
Male SD rats (body weight: 110 to 170 g, one group consisting of 5 rats) were fed ad libitum for 4 days with a diet containing 2 w/w % of cholesterol and 0.5 w/w % of sodium cholate. Then, the rats were further fed ad libitum with the same diet containing 100 mg % or 20 mg % of a test compound. On the other hand, control group of rats were further fed with the diet not containing the test compound. Three days later, the rats were anesthetized with ether. After the body weight of the rats were measured, blood was collected from abdominal aorta thereof. The blood was allowed to stand at room temperature for one hour and centrifuged. Then, the total cholesterol level in the serum thus obtained was measured enzymatically according to the method described in Clinical Chemistry, vol. 20, page 470 (1974). On the other hand, serum HDL-cholesterol was separated from other forms of cholesterol by the lipoprotein sedimentation method using dextran sulfate [Canadian Journal of Biochemistry, vol. 47, page 1043 (1969)], and then measured enzymatically according to the above-described method. On the basis of the results obtained above, the effects of the test compound on the serum total cholesterol level and on serum HDL-cholesterol level were estimated according to the following formulae: ##EQU1##
Results are shown in Table 1 and Table 2 below.
TABLE 1______________________________________ Decrease (%) in serum Increase (%) total in serum HDL-Test compounds cholesterol cholesterol(Amount in the diet: 20 mg %) level level______________________________________1-(3,4-dimethoxyphenyl)-2,3- 52 86bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxy-naphthalene1-(3,4-dimethoxyphenyl)-2,3- 52 23bis(methoxycarbonyl)-4-hydroxy-7,8-methylenedioxy-naphthalene1-(3,4-dimethoxyphenyl)-2,3- 62 80bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxy-naphthalene1-(3,4-dimethoxyphenyl)-3- 51 60hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoicacid lactone______________________________________
TABLE 2______________________________________ Decrease (%) in serum Increase (%) total in serum HDL-Test compounds cholesterol cholesterol(Amount in the diet: 100 mg %) level level______________________________________1-(3,4-dimethoxyphenyl)-3- 63 113hydroxymethyl-4-hydroxy-7-methyl-2-naphthoic acid lactone1-(3,4-dimethoxyphenyl)-2,3- 48 76bis(methoxycarbonyl)-4-hydroxy-7-methylnaphthalene1-(3,4-dimethoxyphenyl)-2,3- 57 93bis(ethoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene1-(3,4-dimethoxyphenyl)-2- 71 178methoxycarbonyl-3-ethoxy-carbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene1-(3,4-dimethoxyphenyl)-2- 68 144ethoxycarbonyl-3-methoxy-carbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene1-(3,4-diethoxyphenyl)-2- 49 44methoxycarbonyl-4-hydroxy-6,7-methylenedioxynaphthalene1-(3,4-diethoxyphenyl)-3- 60 91hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acidlactone1-(3,4-dimethyoxyphenyl)-2,3- 45 57bis(methoxycarbonyl)-4-hydroxy-6-methoxy-7-benzyloxy-naphthalene1-(3,4-dimethoxyphenyl)-3- 37 39hydroxymethyl-4-hydroxy-6-methoxy-2-naphthoic acidlactone1-(3,4-diethoxyphenyl)-2,3- 60 67bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene1-(3,4-dimethoxyphenyl)-3- 32 36hydroxymethyl-4-hydroxy-2-naphthoic acid lactone1-(3,4-dimethoxyphenyl)-2,3- 50 79bis(methoxycarbonyl)-4,8-dihydroxy-6,7-dimethoxy-naphthalene1-(3,4-dimethoxyphenyl)-2,3- 45 64bis(methoxycarbonyl)-4,7-dihydroxy-6,8-dimethoxy-naphthalene1-(3,4-dimethoxyphenyl)-2,3- 56 89bis(methoxycarbonyl)-4,6-dihydroxy-7,8-dimethoxy-naphthalene1-(3,4-dimethoxyphenyl)-2,3- 35 --bis(methoxycarbonyl)-4-hydroxy-6-benzyloxy-7,8-dimethoxy-naphthalene______________________________________
Further, immediately after the collection of blood in the above-mentioned experiment, the liver of each rat was taken out, and the weight thereof was measured. Then, the relative liver weight was examined according to the following formula, and the average relative liver weight was compared with that in the control group. The test compounds used in the above-mentioned experiments caused no substantial increase in the relative liver weight. ##EQU2##

EXAMPLE 1
(1) A solution of 1.55M n-butyl lithium in 430 ml of hexane is added dropwise to a solution of 204.0 g of 2-bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal in 800 ml of tetrahydrofuran. Said addition is carried out at -70.degree. to -50.degree. C. under stirring for about 15 minutes. The mixture is stirred at -70.degree. to -60.degree. C. for 15 minutes. Then, a solution of 105.5 g of 3,4-dimethoxybenzaldehyde in 300 ml of tetrahydrofuran is added to said mixture at -70.degree. to -50.degree. C. for 15 minutes. The mixture is stirred at the same temperature for 15 minutes and then poured into 2 liters of water. 4 liters of ethyl acetate are added to the aqueous mixture. After shaking, the organic layer is separated from the mixture, washed with water, dried and filtered to remove inorganic materials. Then, the organic layer is evaporated under reduced pressure to remove the solvent, whereby 266 g of 2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethylacetal are obtained as yellow syrup.
NMR(CDCl.sub.3) .delta.: 3.25 (s, 6H), 3.80 (s, 6H), 3.89 (s, 3H), 4.05 (d, 1H), 5.35 (s, 1H), 6.20 (d, 1H), 6.6-7.2 (m, 4H)
IR .nu..sub.max.sup.Nujol (cm.sup.1): 3450, 1600
Mass(m/s): 376(M.sup.+ --CH.sub.3 OH)
(2) 266 g of 2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethylacetal are dissolved in 95 ml of benzene. 95 ml of dimethyl acetylenedicarboxylate and 300 mg of p-toluenesulfonic acid.monohydrate are added to the solution. After refluxing for 2 hours, the mixture is cooled and then evaporated under reduced pressure to remove the solvent. 600 ml of methanol are added to the residue, and the mixture is allowed to stand at -30.degree. C. overnight. Crystalline precipitates are collected by filtration and recrystallized from ethyl acetate, whereby 202 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene are obtained as colorless prisms.
m.p. 178.degree.-179.degree. C.
NMR (DMSO-d.sub.6) .delta.: 3.21 (s, 3H), 3.45 (s, 3H), 3.73 (s, 3H), 3.74 (s, 3H), 3.82 (s, 3H), 3.92 (s, 3H), 4.0 (s, 3H), 6.5-7.1 (m, 3H), 7.6 (s, 1H), 11 12.5 (br, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.1): 1730, 1660, 1595, 1510
EXAMPLE 2
(1) 2-bromobenzaldehyde dimethylacetal and 3,4-dimethoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)benzaldehyde dimethylacetal is obtained as pale yellow syrup.
Said syrup is purified by silica gel flash column chromatography [solvent: ethyl acetate-hexane (1:2)] to give colorless syrup. Yield: 89%
NMR (DMSO-d6) .delta.: 3.15 (s, 3H), 3.25 (s, 3H), 3.69 (s, 6H), 5.56 (s, 1H), 5.65 (d, 1H, J=4 Hz), 6.01 (d, 1H), 6.7-7.6 (m, 7H),
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxynaphthalene is obtained as colorless crystals.
M.p. 182.degree.-184.degree. C.
NMR (CDCl.sub.3, .delta.): 3.58 (s, 3H), 3.76 (s, 3H), 3.90 (s, 3H), 3.99 (s, 3H), 6.7-7.2 (m, 3H), 7.4-7.9 (m, 3H), 8.3-8.6 (m, 1H), 11-13 (br, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1660, 1620, 1590, 1520
Mass (m/e): 396 (M.sup.+)
EXAMPLES 3 to 6 ##STR58##
The compounds shown in the following Table 3 are obtained by treating the corresponding starting compounds in the same manner as described in Example 1-(1) & (2).
TABLE 3______________________________________Example Compound [A]Nos. Ring B Physical Properties etc..sup.note)______________________________________ ##STR59## Colorless Crystals, m.p. 199-200.degree. C. Mass (m/e): 410 (M.sup.+)4 ##STR60## Colorless Crystals, m.p. 178-179.degree. C. IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 1725, 1660, 1595, 1580, 1510 Mass (m/e): 426 (M.sup.+)5 ##STR61## Yield: 63% Colorless Crystals, m.p. 208-209.degree. C. .nu. .sub.max.sup.Nujol (cm.sup.-1): 1730, 1660, 1620, 1590, 1510 Mass (m/e): 456 (M.sup.+)6 ##STR62## Yield: 53% Colorless Crystals, m.p. 172-174.degree. C. IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 1730, 1660, 1620, 1590, 1510 Mass (m/e): 532 (M.sup.+)______________________________________
Note: NMR spectrum data of the compounds shown in Table 3 are as follows.
The compound of Example 3 (DMSO-d.sub.6 +CF.sub.3 COOD, .delta.): 2.40 (s, 3H), 3.55 (s, 3H), 3.76 (s, 3H), 3.88 (s, 3H), 3.95 (s, 3H), 6.7-7.2 (m, 3H), 7.2-7.6 (m, 3H), 8.35 (d, 1H, J=9 Hz)
The compound of Example 4 (DMSO-d.sub.6, .delta.): 3.55 (s, 3H), 3.75 (s, 3H), 3.85 (s, 3H), 3.95 (s, 6H), 6.7-7.8 (m, 6H)
The compound of Example 5 (DMSO-d.sub.6, .delta.): 3.55 (s, 3H), 3.68 (s, 3H), 3.78 (s, 3H), 3.88 (s, 3H), 3.93 (s, 3H), 3.97 (s, 3H), 6.7-7.0 (m, 3H), 7.10 (d, 1H, J=8 Hz), 7.66 (s, 1H), 10-12 (br, 1H),
The compound of Example 6 (CDCl.sub.3, .delta.): 3.55 (s, 3H), 3.79 (s, 3H), 3.90 (s, 3H), 4.00 (s, 3H), 4.05 (s, 3H), 5.01 (s, 2H), 6.65 (s, 1H), 6.75 (s, 1H), 6.72 (d, 1H, J=8 Hz), 6.90 (d, 1H, J=8 Hz), 7.20 (s, 5H), 7.70 (s, 1H)
Example 7
(1) 2-bromo-4,5-methylenedioxybenzaldehyde dimethylacetal and 3,4-diethoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)-4,5-methylenedioxybenzaldehyde dimethylacetal is obtained as colorless syrup. Yield 76%
NMR (DMSO-d6) .delta.: 1.29 (t, 6H), 3.13 (s, 3H), 3.23 (s, 3H), 3.95 (q, 4H), 5.49 (s, 1H) 5.60 (d, 1H, J=5 Hz), 5.9-6.1 (m, 3H), 6.7-7.1 (m, 5H)
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene is obtained as colorless crystals.
M.p. 158.degree.-159.degree. C.
NMR (CDCl.sub.3, .delta.): 1.40 (t, 3H), 1.48 (t, 3H), 3.50 (s, 3H), 3.91 (s, 3H), 4.10 (q, 2H), 4.15 (q, 2H), 6.00 (s, 2H), 6.72 (s, 1H), 6.78 (d, 1H, J=9 Hz), 6.80 (s, 1H), 6.95 (d, 1H, J=9 Hz), 7.70 (s, 1H), 12.12 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1750, 1660, 1620, 1600, 1595
Mass (m/e): 468 (M.sup.+)
Example 8 to 9 ##STR63##
The compounds shown in the following Table 4 are obtained by treating the corresponding starting compounds in the same manner as described in Example 1-(1) & (2).
TABLE 4______________________________________Example Compound [B]Nos. R.sup.12 /R.sup.5 Physical Properties etc..sup.(note)______________________________________8 R.sup.12 = COOC.sub.2 H.sub.5 Yield: 59% R.sup.5 = C.sub.2 H.sub.5 Colorless Crystals m.p. 150-151.degree. C. IR.nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1640, 1620, 1600, 1580, 1520, 1500 Mass (m/e): 496 (M.sup.+)9 R.sup.12 = H Yield: 59% R.sup.5 = C.sub.2 H.sub.5 m.p. 169-171.degree. C. IR.nu..sub.max.sup.Nujol (cm.sup.-1): 3400, 1670, 1625, 1580, 1540, 1515 Mass (m/e): 424 (M.sup.+)______________________________________
Note: NMR spectrum data of the compounds shown in Table 4 are as follows.
The compound of Example 8 (CDCl.sub.3, .delta.): 1.01 (t, 3H), 1.38 (t, 3H), 1.45 (t, 3H), 1.50 (t, 3H), 4.02 (q, 2H), 4.10 (q, 2H), 4.20 (q, 2H), 4.40 (q, 2H), 6.04 (s, 2H), 6.79 (s, 1H), 6.82 (d, 1H, J=9 Hz), 6.85 (s, 1H), 6.97 (d, 1H), 7.72 (s, 1H), 12.32 (s, 1H)
The compound of Example 9 (CDCl.sub.3, .delta.): 0.93 (t, 3H), 1.41 (t, 3H), 1.50 (t, 3H), 3.9-4.4 (m, 6H), 6.00 (s, 2H), 6.7-7.3 (m, 4H), 7.38 (s, 1H), 7.6 (s, 1H)
Example 10
2-Bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal, 3,4-dimethoxybenzaldehyde and diethyl acetylenedicarboxylate are treated in the same manner as described in Example 1-(1) and (2), whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene is obtained as colorless crystals.
m.p. 138.degree.-140.degree. C.
NMR (CDCl.sub.3) .delta.: 1.05 (t, 3H), 1.40 (t, 3H), 3.31 (s, 3H), 3.90 (s, 3H), 3.95 (s, 3H), 3.95 (q, 2H), 3.97 (s, 3H), 4.10 (s, 3H), 4.45 (q, 2H), 6.90 (s, 3H), 7.72 (s, 1H), 12.59 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1735, 1720, 1655, 1590, 1510
Mass (m/e): 514 (M.sup.+)
Example 11
(1) 2-bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal and 3,4-diethoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(3,4-diethoxyphenyl-.alpha.-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethylacetal is obtained as pale yellow syrup.
Said syrup is purified by silica gel flash column chromatography [solvent: ethyl acetate-hexane (1:2)] to give colorless syrup. Yield: 76%
NMR (DMSO-d6).delta.: 1.27 (t, 6H), 2.86 (s, 3H), 3.27 (s, 3H), 3.58 (d, 1H, J=5 Hz), 3.60 (s, 3H), 3.74 (s, 3H), 3.76 (s, 3H), 3.89 (q, 2H), 3.94 (q, 2H), 5.48 (s, 1H), 6.10 (d, 1H), 6.5-7.0 (m, 4H)
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(3,4-diethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-methylenedioxynaphthalene is obtained as colorless crystals.
M.p. 138.degree.-140.degree. C.
NMR (CDCl.sub.3, .delta.): 1.05 (t, 3H), 1.40 (t, 3H), 3.31 (s, 3H), 3.90 (s, 3H), 3.95 (s, 3H), 3.97 (s, 3H), 4.10 (s, 3H), 4.15 (q, 2H), 4.20 (q, 2H), 6.7-7.0 (m, 3H), 7.69 (s, 1H), 12.36 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1660, 1590, 1510
Mass (m/e): 514 (M.sup.+)
Example 12
(1) 2-bromo-4,5-methylenedioxybenzaldehyde dimethylacetal and 4-methoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(4-methoxy-.alpha.-hydroxybenzyl)-4,5-methylenedioxybenzaldehyde dimethylacetal is obtained as colorless syrup. Yield: 82%
NMR (DMSO-d6).delta.: 3.10 (s, 3H), 3.22 (s, 3H), 3.70 (s, 3H), 5.46 (s, 1H), 5.61 (d, 1H, J=4 Hz), 5.85-6.15 (m, 3H), 6.7-7.4 (m, 6H)
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(4-methoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene is obtained as colorless crystals.
M.p. 169.degree.-171.degree. C.
NMR (CDCl.sub.3, .delta.): 3.55 (s, 3H), 3.88 (s, 3H), 3.95 (s, 3H), 6.03 (s, 2H), 6.72 (s, 1H), 6.9-7.4 (m, 4H), 7.75 (s, 1H), 12.20 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1660, 1610, 1520
Mass (m/e): 410 (M.sup.+)
Example 13
(1) A solution of 7 g of 3,4-dihydroxybenzaldehyde in 20 ml of dimethyformamide is added dropwise to a mixture of 4.8 g of 60% sodium hydride in 70 ml of dimethylformamide over a period of 15 minutes under ice-cooling. The mixture is stirred at the same temperature for 15 minutes. Then, 50 g of n-propyl iodide are added thereto. After stirring for 12 hours, the mixture is evaporated to remove the solvent. The residue is extracted with ether and the extract is washed with water, dried, filtered to remove inorganic materials and then evaporated to remove the solvent, whereby 8.5 g of 3,4-dipropoxybenzaldehyde are obtained as pale yellow oil.
b.p. 130.degree.-136.degree. C. (at 0.2 mmHg)
(2) 2-Bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal, 3,4-dipropoxybenzaldehyde and dimethyl acetylenedicarboxylate are treated in the same manner as described in Example 1-(1) and (2), whereby 1-(3,4-dipropoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene is obtained as colorless needles.
m.p. 132.degree. C.
NMR (CDCl.sub.3) .delta.: 0.99 (t, 3H), 1.05 (t, 3H), 1.6-2.1 (m, 4H), 3.21 (s, 3H), 3.42 (s, 3H), 3.73 (s, 3H), 3.77 (s, 3H), 3.89 (s, 3H), 3.8-4.2 (m, 4H), 6.74 (s, 1H), 6.76 (s, 2H), 7.59 (s, 1H), 12.25 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1660, 1570, 1510
Example 14
(1) A solution of 1.55M n-butyl lithium in 20 ml of hexane is added dropwise to a solution of 9.24 g of N-(3,4-methylenedioxybenzylidene)cyclohexylamine in 100 ml of tetrahydrofuran. Said addition is carried out at -70.degree. to -60.degree. C. under stirring for 15 minutes. After the mixture is stirred at the same temperature for further 15 minutes, a solution of 6.65 g of 3,4-dimethoxybenzaldehyde in 15 ml of tetrahydrofuran is added dropwise to the mixture at the same temperature over a period of 15 minutes. The mixture is further stirred at the same temperature for 15 minutes and then poured into a mixture of 300 ml of water and 300 ml of ethyl ether. The organic layer is separated from the mixture, washed with water, dried and evaporated under reduced pressure to remove the solvent. The yellow syrup thus obtained is subjected to column chromatography on silica gel [solvent; benzene-ethyl ether (4:1) saturated with water], and the eluate is evaporated under reduced pressure to remove the solvent. The resultant colorless crystals are recrystallized from a mixture of ethyl acetate and hexane, whereby 8.7 g 3,4-methylenedioxy-2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)benzaldehyde are obtained as colorless needles. Yield: 69%
m.p. 129.degree.-130.degree. C.
NMR (CDCl.sub.3) .delta.: 3.55 (d, 0.3H, J=9 Hz), 3.70 (d, 0.4H, J=9Hz), 5.45 (d, 0.3H, J=10 Hz), 3.85 (s, 3H), 3.86 (s, 3H), 5.90 (close m, 2H), 6.0-7.5 (m, 6.7H), 9.70 (s, 0.3H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3410, 3300, 1610, 1520
Mass (m/e): 316 (M.sup.+)
(2) 6.5 g of 3,4-methylenedioxy-2-(3,4-dimethoxy-.alpha.-hydroxybenzyl)benzaldehyde are dissolved in 10.5 ml of benzene under heating. 6.5 ml of dimethyl acetylenedicarboxylate and 3 mg of p-toluenesulfonic acid.monohydrate are added to the solution. The mixture is refluxed for 30 minutes. After cooling to room temperature, 300 ml of methanol are added to the mixture, and the mixture is allowed to stand at -30.degree. C. overnight. Crystalline precipitates are collected by filtration and recrystallized from a mixture of tetrahydrofuran and methanol, whereby 7.5 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-7,8-methylenedioxynaphthalene are obtained as pale yellow prisms. Yield: 83%
m.p. 228.degree.-229.degree. C.
NMR (DMSO-d.sub.6) .delta.: 3.50 (s, 3H), 3.74 (s, 3H), 3.82 (s, 3H), 3.91 (s, 3H), 5.92 (s, 2H), 6.7-7.05 (m, 3H), 7.40 (d, 1H, J=9 Hz), 8.05 (d, 1H, J=9 Hz)
IR.nu..sub.max.sup.Nujol (cm.sup.-1): 1730, 1659, 1630, 1590, 1510 (br)
Mass (m/e): 440 (M.sup.+)
Example 15
(1) 1.75 g of 3,4-dichlorobenzaldehyde and 11.88 g of cyclohexylamine are dissolved in 100 ml of benzene. The mixture is refluxed for 4 hours while removing the resultant water with Dien-Stark dehydrating aparatus. The reaction mixture is evaporated to dryness under reduced pressure, whereby 25 g of N-(3,4-dichlorobenzylidene)cyclohexylamine are obtained as pale yellow syrup. Yield: 98%
NMR (CDCl.sub.3) .delta.: 1.0-2.2 (m, 10H), 3.0-3.4 (m, 1H), 7.15 (s, 1H), 7.2-7.8 (m, 3H)
(2) A solution of 1.55M n-butyl lithium in 27 ml of hexane is added dropwise to a solution of 10.24 g of N-(3,4-dichlorobenzylidene)cyclohexylamine in 100 ml of tetrahydrofuran. Said addition is carried out at -70.degree. C. under stirring for 15 minutes. After the mixture is stirred at -70 .degree. to -60.degree. C. for further 9 minutes, a solution of 6.65 g of 3,4-dimethoxybenzaldehyde in 20 ml of tetrahydrofuran is added to said mixture at -70 .degree. to -50.degree. C. over a period of 15 minutes. After stirring the mixture at the same temperature for further 15 minutes, said mixture is poured into a mixture of 300 ml of water and 300 ml of ethyl ether. The organic layer is separated from the mixture, washed with water, dried and then evaporated under reduced pressure to remove the solvent. The yellow syrup thus-obtained is subjected to column chromatography on silica gel [solvent; ethyl acetatehexane (1:2)], whereby 8.6 g of 1-(3,4-dimethoxyphenyl)-3-cyclohexylamino-6,7-dichlorophthalane are obtained as colorless crystals. Yield: 51%
m.p. 68.degree.-69.degree. C.
NMR (CDCl.sub.3) .delta.: 0.8-2.3 (m, 11H), 2.7-3.1 (m, 1H), 3.82 (s, 3H), 3.85 (s, 3H), 5.9-6.4 (m, 2H),
6.6-7.0 (m, 3H), 7.22 (d, 1H, J=6 Hz), 7.45 (d, 1H, J=6 Hz),
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3300, 1595, 1510
(3) 2.1 g of 1-(3,4-dimethoxyphenyl)-3-cyclohexylamino-6,7-dichlorophthalane are dissolved in 3 ml of hexamethylphosphoryltriamide. 0.38 ml of methyl iodide and 0.76 g of potassium carbonate are added to the solution. The mixture is stirred at room temperature for 12 hours. 50 ml of ethyl acetate are added to the reaction mixture. The mixture is washed with water, and the organic layer is separated from the mixture, dried and evaporated under reduced pressure to remove the solvent, whereby 2.1 g of 1-(3,4-dimethoxyphenyl)-3-(N-methyl-N-cyclohexylamino)-6,7-dichlorophthalane are obtained as yellow oil.
(4-a) 2.0 g of 1-(3,4-dimethoxyphenyl)-3-(N-methyl-N-cyclohexylamino)-6,7-dichlorophthalane are dissolved in a mixture of 2.3 ml of benzene and 2 ml of dimethyl acetylenedicarboxylate. 0.4 ml of methanesulfonic acid is added to the solution. The mixture is refluxed for 2 hours under stirring. After cooling the reaction mixture to room temperature, 100 ml of methanol are added to said mixture. The mixture is allowed to stand at -30.degree. C. for 12 hours. Crystalline precipitates are collected by filtration and recrystallized from ethyl acetate, whereby 1.9 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-7,8-dichloronaphthalene are obtained as colorless prisms. Yield: 83% [overall yield from 1-(3,4-dimethoxyphenyl)-3-cyclohexylamino-6,7-dichlorophthalane]
m.p. 209.degree.-210.degree. C.
NMR (DMSO-d.sub.6) .delta.: 3.50 (s, 3H), 3.75 (s, 3H), 3.85 (s, 3H), 3.95 (s, 3H), 6.6-7.1 (m, 3H), 7.8 (d, 1H, J=9 Hz), 8.4 (d, 1H, J=9 Hz), 11.98 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1730, 1660, 1605, 1580, 1510
(4-b) 4.42 g of 1-(3,4-dimethoxyphenyl)-3-cyclohexylamino-6,7-dichlorophthalane, 4 ml of benzene, 3 ml of dimethyl acetylenedicarboxylate and 0.96 ml of methanesulfonic acid are treated in the same manner as described in paragraph (4-a), whereby 3.34 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-7,8-dichloronaphthalene are obtained. Yield: 72%
Physical properties of the product are identical with those of the product obtained in paragraph (4-a).
Example 16
(1) 2.34 g of 1-(3,4-diethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene are dissolved in a solution of 2.8 g of potassium hydroxide in a mixture of 20 ml of water and 10 ml of methanol. The solution is refluxed under stirring for 2 hours. 2.8 g of potassium hydroxide are further added to the solution, and the mixture is refluxed for further 24 hours. The mixture is cooled and then 50 ml of chloroform are added thereto. After shaking, the aqueous layer is separated from the mixture and adjusted to pH 1 with 12N hydrochloric acid. Crystalline precipitates are collected by filtration and washed with water and methanol, whereby 1.8 g of 1-(3,4-diethoxyphenyl)-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid are obtained as colorless crystals. Yield: 96%
m.p. 284.degree. C. (decomp.)
NMR (DMSO-d.sub.6) .delta.: 1.31 (t, 3H), 1.40 (t, 3H), 4.05 (q, 2H), 4.13 (q, 2H), 6.11 (s, 2H), 6.6-7.1 (m, 4H), 7.12 (s, 1H), 7.50 (s, 1H), 10.23 (br m, 1H), 12.3 (br, 1H),
Mass (m/e): 396 (M.sup.+)
(2) 1.7 g of 1-(3,4-diethoxyphenyl)-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid are dissolved in a mixture of 150 ml of methanol and 100 ml of dioxane. 10 ml of thionyl chloride are added to the solution at room temperature. The mixture is stirred at room temperature for 12 hours, and then evaporated under reduced pressure to remove the solvent, whereby 1.6 g of 1-(3,4-diethoxyphenyl)-2-methoxycarbonyl-4-hydroxy-6,7-methylenedioxynaphthalene are obtained as colorless crystals. Yield: 91%
m.p. 189.degree.-190.degree. C. (recrystallized from methanol)
NMR (CDCl.sub.3) .delta.: 1.38 (t, 3H), 1.44 (t, 3H), 3.53 (s, 3H), 4.05 (q, 2H), 4.13 (q, 2H), 5.93 (s, 2H), 6.6-7.0 (m, 4H), 7.21 (s, 1H), 7.50 (s, 1H)
Example 17
0.7 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-7-methylnaphthalene obtained in Example 3 is dissolved in 30 ml of tetrahydrofuran. 0.24 ml of borane-methylsulfide complex is added to the solution. The mixture is refluxed for 4 hours. After cooling, the reaction mixture is evaporated to dryness under reduced pressure. The residue is dissolved in 300 ml of methanol containing trifluoroacetic acid. The solution is allowed to stand at room temperature for 12 hours, and crystalline precipitates are collected by filtration, whereby 450 mg of 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-7-methyl-2-naphthoic acid lactone are obtained as colorless needles. Yield: 76%
m.p. 234.degree.-236.degree. C.
NMR (DMSO-d.sub.6) .delta.: 2.4 (s, 3H), 3.75 (s, 3H), 3.89 (s, 3H), 5.40 (s, 2H), 6.7-8.4 (m, 6H), 10.2-10.7 (br, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3500, 1730, 1660, 1620, 1590, 1515
Mass (m/e): 350 (M.sup.+)
Example 18 to 22 ##STR64##
The compounds shown in the following Table 5 are obtained by treating the corresponding starting compounds in the same manmer as described in Example 17.
TABLE 5______________________________________Example Compound [C]Nos. Ring E Physical Properites etc..sup.note)______________________________________18 ##STR65## Yield: 98% Colorless Crystals, m.p. 260.degree. C. (decomp.) IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 1740, 1630, 1600, 1520 Mass (m/e): 336 (M.sup.+)19 ##STR66## Yield: 92% Colorless Crystals m.p. 254.degree. C. (decomp.) IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 3200, 1740, 1620, 1580, 1520 Mass (m/e): 366 (M.sup.+)20 ##STR67## Yield: 92% Colorless Crystals m.p. 261.degree. C. (decomp.) IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 3200, 1740 1720, 1620, 1600, 1590, 1540 Mass (m/e): 426 (M.sup.+)21 ##STR68## Yield: 91% Yellow crystals m.p. 273.degree. C. (decomp.) IR.nu. .sub.max.sup.Nujol (cm.sup.-1): 3420, 1730, 1620, 1590, 1540, 1510 Mass (m/e): 380 .sup.(M.sup.+)22 ##STR69## Yield: 85% Colorless Crystals m.p. 243.degree. C. (decomp.) Mass (m/e): 472 (M.sup.+)______________________________________
Note: NMR spectrum data of the compounds shown in Table 5 are as follows.
The compound of Example 18 (DMSO-d.sub.6, .delta.): 3.77 (s, 3H), 3.90 (s, 3H), 5.46 (s, 2H), 6.8-7.3 (m, 3H), 7.4-7.9 (m, 3H), 8.3-8.5 (m, 1H)
The compound of Example 19 (DMSO-d.sub.6, .delta.): 3.69 (s, 3H), 3.90 (s, 3H), 4.00 (s, 3H), 5.45 (s, 2H), 6.8-7.3 (m, 4H), 7.6-7.9 (m, 2H)
The compound of Example 20 (DMSO-d.sub.6, .delta.): 3.22 (s, 3H), 3.71 (s, 3H), 3.80 (s, 3H), 3.82 (s, 3H), 4.00 (s, 3H), 5.35 (s, 2H), 6.6-7.1 (m, 3H), 7.55 (s, 1H), 10.45 (s, 1H)
The compound of Example 21 (DMSO-d.sub.6, .delta.): 3.75 (s, 3H), 3.85 (s, 3H), 5.35 (s, 2H), 5.91 (s, 2H), 6.0-7.1 (m, 3H), 7.40 (d, 1H, J=8 Hz), 8.00 (d, 1H, J=8 Hz), 10-11 (br, 1 H)
The compound of Example 22 (DMSO-d.sub.6, .delta.): 3.75 (s, 3H), 3.91 (s, 3H), 4.00 (s, 3H), 5.00 (s, 2H), 5.38 (s, 2H), 6.6-7.1 (m, 4H), 7.30 (s, 5H), 7.65 (s, 1H), 10.0-10.6 (br, 1H)
Example 23 and 24 ##STR70##
The compounds shown in the following Table 6 are obtained by treating the corresponding starting compounds in the same manner as described in Example 17.
TABLE 6______________________________________Example Compound [D]Nos. R.sup.33 /R.sup.43 Physical Properties etc..sup.(note)______________________________________23 R.sup.33 = R.sup.43 Yield: 62% = OC.sub.2 H.sub.5 Colorless Crystals m.p. 251.degree. C. (decomp.) IR.nu..sub.max.sup.Nujol (cm.sup.-1): 3300, 1760, 1630, 1580, 1540, 1520, 1500 Mass (m/e): 408 (M.sup.+)24 R.sup.33 = H Yield: 87% R.sup.43 = OCH.sub.3 Colorless Crystals m.p. 297.degree. C. (decomp.) IR.nu..sub.max.sup.Nujol (cm.sup.-1): 3150, 1720, 1620, 1540, 1520 Mass (m/e): 350 (M.sup.+)______________________________________
Note: NMR spectrum data of the compounds shown in Table 6 are as follows.
The compound of Example 23 (DMSO-d.sub.6, .delta.): 1.31 (t, 3H), 1.40 (t, 3H), 4.05 (q, 2H), 4.10 (q, 2H), 5.35 (s, 2H), 6.15 (s, 2H), 6.89 (s, 1H), 6.6-7.2 (m, 3H), 7.6 (s, 1H), 10.31 (s, 1H)
The Compound of Example 24 (DMSO-d.sub.6, .delta.): 3.89 (s, 3H), 5.39 (s, 2H), 6.18 (s, 2H), 6.85 (s, 1H), 7.0-7.4 (m, 4H), 7.65 (s, 1H)
Example 25
1-(3,4-Diethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphtalene is treated in the same manner as described in Example 17, whereby 1-(3,4-diethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7,8-trimethoxy-2-naphthoic acid lactone is obtained as colorless crystals. Yield: 84%
m.p. 219.degree. C. (decomp.)
NMR (DMSO-d.sub.6) .delta.: 1.32 (t, 3H), 1.40 (t, 3H), 3.22 (s, 3H), 3.81 (s, 3H), 4.01 (s, 3H), 4.03 (q, 2H), 4.11 (q, 2H), 5.35 (s, 2H), 6.6-7.0 (m, 3H), 7.56 (s, 1H), 10.40 (br s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3300, 1760, 1605, 1500
Mass (m/e): 454 (M.sup.+)
Example 26
1-(3,4-Dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-7,8-dichloronaphthalene is treated in the same manner as described in Example 17, whereby 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-7,8-dichloro-2-naphthoic acid lactone is obtained as pale yellow crystals. Yield: 62%
m.p. 260.degree. C. (decomp.)
NMR (DMSO-d.sub.6) .delta.: 3.64 (s, 3H), 3.79 (s, 3H), 5.30 (s, 2H), 6.5-7.0 (m, 3H), 7.65 (d, 1H, J=9 Hz), 8.25 (d, 1H, J=9 Hz), 10.85 (br s, 1H),
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3200, 1725, 1620, 1595, 1510
Example 27
1-(3,4-Dipropoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene obtained in Example 13 is treated in the same manner as described in Example 17, whereby 1-(3,4-dipropoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7,8-trimethoxy-2-naphthoic acid lactone is obtained as colorless crystals.
m.p. 129.degree.-132.degree. C.
NMR (CDCl.sub.3 +DMSO-d.sub.6) .delta.: 0.99 (t, 3H), 1.04 (t, 3H), 1.6-2.1 (m, 4H), 3.26 (s, 3H), 3.85 (s, 3H), 3.95 (s, 3H), 3.7-4.2 (m, 4H), 5.25 (s, 2H), 6.75 (s, 2H), 6.80 (s, 1H), 7.49 (s, 1H), 9.50 (br s, 1H)
Example 28
9.72 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene obtained in Example 1 are added to a sodium ethoxide solution prepared from 500 ml of ethanol and 2.76 g of sodium metal. The mixture is refluxed for 3 hours. The reaction mixture is cooled, and then 7.2 ml of acetic acid are added thereto. The mixture is evaporated to dryness under reduced pressure. The residue is dissolved in 200 ml of chloroform. The chloroform solution is washed with water, dried, filtered to remove inorganic materials and then evaporated to remove the solvent. Crystalline precipitates thus obtained are recrystallized from ethyl acetate, whereby 7.2 g of 1-(3,4-dimethoxyphenyl)-2-methoxycarbonyl-3-ethoxycarbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene are obtained as colorless prisms.
m.p. 151.degree.-152.degree. C.
NMR (CDCl.sub.3) .delta.: 1.31 (t, 3H), 3.22 (s, 3H), 3.41 (s, 3H), 3.80 (s, 3H), 3.87 (s, 3H), 3.90 (s, 3H), 4.00 (s, 3H), 4.35 (q, 2H), 6.76 (s, 3H), 7.60 (s, 1H), 12.42 (s, 1H)
Example 29
1-(3,4-dimethoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene obtained in Example 10 is treated with a sodium methoxide solution in the same manner as described in Example 28, whereby 1-(3,4-dimethoxyphenyl)-2-ethoxycarbonyl-3-methoxycarbonyl-4-hydroxy-6,7,8-trimethoxynaphthalene is obtained as colorless prisms.
m.p. 157.degree.-159.degree. C.
NMR (CDCl.sub.3) .delta.: 1.03 (t, 3H), 3.22 (s, 3H), 3.8 (s, 3H), 3.75 (s, 3H), 3.87 (s, 6H), 3.9 (q, 2H), 3.98 (s, 3H), 6.77 (s, 3H), 7.59 (s, 1H), 12.29 (s, 1H)
Example 30
(1) 2-bromo-4,5-methylenedioxybenzaldehyde dimethylacetal and 3-methyoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(3-methoxy-.alpha.-hydroxybenzyl)-4,5-methylenedioxybenzaldehyde dimethylacetal is obtained as pale yellow syrup. Yield: 79%
NMR (DMSO-d6).delta.: 3.13 (s, 3H), 3.23 (s,3H), 3.69 (s, 3H), 5.50 (s, 1H), 5.68 (d, 1H, J=4 Hz), 5.9-6.1 (m, 3H), 6.6-7.4 (m, 6H)
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(3-methoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene is obtained as colorless crystals.
m.p. 152.degree.-154.degree. C.
NMR (CDCl.sub.3, .delta.): 3.5 (s, 3H), 3.80 (s, 3H), 3.90 (s, 3H), 6.15 (s, 2H), 6.60 (s, 1H), 6.7-6.9 (m, 2H), 6.9-7.2 (m, 1H), 7.4 (d, 1H), 7.57 (s, 1H), 11-12 (br, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1730, 1660, 1610, 1600
Mass (m/e): 410 (M.sup.+)
Example 31
2-Bromo-4,5-methylenedioxybenzaldehyde dimethylacetal, 3,4-diisopropoxybenzaldehyde and diethyl acetylenedicarboxylate are treated in the same manner as described in Example 1, whereby 1-(3,4-diisopropoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene is obtained. Yield: 51%
m.p. 123.degree.-124.degree. C.
Mass (m/e): 524 (M.sup.+)
NMR (DMSO-d.sub.6) .delta.: 0.94 (t, 3H), 1.35 (t, 3H), 1.30 (d, 6H), 1.36 (d, 6H), 3.96 (q, 2H), 4.35 (q, 2H), 4.3-4.7 (m, 2H), 6.09 (s, 2H), 6.6-7.1 (m, 4H), 7.55 (s, 1H), 12.19 (s, 1H)
Example 32
1-(3-methoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene obtained in Example 30 is treated in the same manner as described in Example 17, whereby 1-(3-methoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid lactone is obtained. Yield: 90%
m.p. 275.degree. C. (decomp.)
IR.nu..sub.max.sup.Nujol (cm.sup.-1): 3200, 1740, 1720, 1620, 1600, 1590, 1540
Mass (m/e): 350 (M.sup.+)
NMR (DMSO-d.sub.6) .delta.: 3.80 (s, 3H), 5.40 (s, 2H), 6.15 (s, 2H), 6.0 (s, 1H), 6.8-7.2 (m, 3H), 7.4 (d, 1H), 7.65 (s, 1H), 11.4 (br s, 1H)
Example 33
1-(3,4-diisopropoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene obtained in Example 31 is treated in the same manner as described in Example 17, whereby 1-(3,4-diisopropoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid lactone is obtained. Yield: 82%
m.p. 223.degree. C.
NMR (CDCl.sub.3) .delta.: 1.33 (d, 6H), 1.40 (d, 6H), 4.3-4.8 (m, 2H), 5.33 (s, 2H), 6.02 (s, 3H), 6.7-7.1 (m, 4H), 7.64 (s, 1H), 8-10 (br, 1H)
Example 34
2 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6-methoxy-7-benzyloxynaphthalene obtained in Example 6 are dissolved in a mixture of 200 ml of tetrahydrofuran and 50 ml of methanol. The solution is stirred in the presence of 2 g of 10% palladium-charcoal in hydrogen atmosphere at 40 psi for 2 hours. After the reaction, the catalyst is removed by filtration, and the filtrate is evaporated to dryness under reduced pressure. The resultant crude crystals are triturated with methanol, whereby 1.5 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6-methoxy-7-hydroxynaphthalene is obtained.
m.p. 231.degree. C. (decomp.)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3400, 1730, 1650, 1620, 1600, 1590, 1580, 1510
NMR (DMSO-d.sub.6) .delta.: 3.5 (s, 3H), 3.74 (s, 3H), 3.82 (s, 3H), 3.90 (s, 3H), 3.95 (s, 3H), 6.6-7.1 (m, 4H), 7.61 (s, 1H), 9.7-10.4 (br, 1H)
Example 35
1-(3,4-Dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6-methoxy-7-benzyloxy-2-naphthoic acid lactone obtained in Example 22 is treated in the same manner as described in Example 34, whereby 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4,7-dihydroxy-6-methoxy-2-naphthoic acid lactone is obtained as colorless microneedles.
m.p. >270.degree. C.
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3420, 1750, 1620, 1600, 1580 (sharp), 1510
Mass (m/e): 382 (M.sup.+)
NMR (DMSO-d.sub.6) .delta.: 3.77 (s, 3H), 3.89 (s, 3H), 3.99 (s, 3H), 5.35 (s, 2H), 6.7-7.3 (m, 4H), 7.6 (s, 1H), 9.0-11.5 (br, 2H)
Example 36
(1) 2-bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal and 3-methoxy-4-ethoxybenzaldehyde are reacted in the same manner as described in Example 1-(1), whereby 2-(3-methoxy-4-ethoxy-.alpha.-hydroxybenzyl)-3,4,5-trimethoxybenzaldehyde dimethylacetal is obtained as colorless syrup. Yield: 84%
NMR (DMSO-d6).delta.: 1.26 (t, 3H), 2.89 (s, 3H), 3.26 (s, 3H), 3.58 (d, 1H, J=5 Hz), 3.61 (s, 3H), 3.68 (s, 3H), 3.74 (s, 3H), 3.78 (s, 3H), 3.93 (q, 2H), 5.49 (s, 1H), 6.11 (d, 1H), 6.5-7.0 (m, 4H)
(2) The product obtained in paragraph (1) and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 1-(2), whereby 1-(3-methoxy-4-ethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene is obtained as colorless crystals.
M.p. 159.degree. C.
NMR (CDCl.sub.3, .delta.): 1.47 (t, 3H), 3.22 (s, 3H), 3.42 (s, 3H), 3.80 (s, 3H), 3.85 (s, 3H), 3.87 (s, 3H), 4.00 (s, 3H), 4.12 (q, 2H), 6.75 (s, 3H), 7.56 (s, 1H), 12.21 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1730, 1710, 1660, 1590, 1510
Example 37
2-Bromo-3,4,5-trimethoxybenzaldehyde dimethylacetal, 3-ethoxy-4-methoxybenzaldehyde and dimethyl acetylenedicarboxylate are treated in the same manner as described in Example 1, whereby 1-(3-ethoxy-4-methoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene is obtained as colorless needles. Yield: 65%
m.p. 158.degree. C.
NMR (CDCl.sub.3) .delta.: 3.42 (t, 3H), 3.22 (s, 3H), 3.45 (s, 3H), 3.85 (s, 3H), 3.89 (s, 3H), 3.98 (s, 3H), 4.08 (q, 2H), 6.76 (s, 3H), 7.56 (s, 1H), 12.21 (s, 1H)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1740, 1655, 1590, 1510
Example 38
2-Bromo-4,5-methylenedioxybenzaldehyde dimethylacetal, 3,4-dimethoxybenzaldehyde and dimethyl acetylenedicarboxylate are treated in the same manner as described in Example 1, whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene is obtained as colorless crystals.
m.p. 130.degree.-133.degree. C.
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 1730, 1672, 1595, 1520
Mass (m/e): 440 (M.sup.+)
NMR (CDCl.sub.3) .delta.: 3.55 (s, 3H), 3.85 (s, 3H), 3.90 (s, 3H), 3.95 (s, 3H), 6.03 (s, 2H), 6.77 (s, 1H), 6.85-6.95 (m, 3H), 7.75 (s, 1H), 12.30 (s, 1H)
Example 39
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-dimethoxynaphthalene obtained in Example 5 is treated in the same manner as described in Example 17, whereby 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-dimethoxy-2-naphthoic acid lactone is obtained as colorless crystals. Yield: 82%
m.p. 278.degree. C. (decomp.)
IR .nu..sub.max.sup.Nujol (cm.sup.-1): 3150, 1740 (sharp), 1700, 1620, 1600, 1580
Mass (m/e): 396 (M.sup.+)
NMR (DMSO-d.sub.6) .delta.: 3.70 (s, 3H), 3.80 (s, 3H), 3.90 (s, 3H), 4.0 (s, 3H), 5.39 (s, 2H), 6.8-7.2 (m, 3H), 7.08 (s, 1H), 7.67 (s, 1H)
EXAMPLE 40
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-methylenedioxynaphthalene obtained in Example 38 is treated in the same manner as described in Example 17, whereby 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-4-hydroxy-6,7-methylenedioxy-2-naphthoic acid lactone is obtained as colorless crystals. Yield: 52%
m.p. 256.degree. C. (decomp.)
Physical properties of this compound are identical with those described in Tetrahedron vol. 34, page 1011 (1978).
EXAMPLE 41
(1) 1.93 g of 62.6% sodium hydride are suspended in 30 ml of dimethylformamide. A solution of 11 g of 2-bromo-3,5-dimethoxy-4-hydroxybenzaldehyde in 140 ml of dimethylformamide are added thereto under stirring at 0.degree. to 5.degree. C. for 20 minutes. The mixture stirred at room temperature for one hour. 7.9 g of benzyl bromide are added thereto. The mixture is stirred at room temperature overnight and evaporated under reduced pressure to remove the solvent. The residue is extracted with 500 ml of ether. The extract is washed with water, dried and evaporated to remove the solvent. The residue is recrystallized from a mixture of methanol and water, whereby 10.5 g of 2-bromo-3,5-dimethoxy-4-benzyloxybenzaldehyde are obtained as colorless crystals.
M.p. 53.degree. C.
(2) A mixture of 68.7 g of the product obtained in paragraph (1), 75 ml of methanol, 100 ml of trimethoxymethane and one g of ion-exchange resin Amberlite IR-120(H.sup.+) are refluxed under heating for 3 hours and filtered to remove insoluble materials. The filtrate is evaporated to remove the solvent, whereby 78 g of 2-bromo-3,5-dimethoxy-4-benzyloxybenzaldehyde dimethylacetal are obtained as yellow syrup.
(3) 6.3 g of the product obtained in paragraph (2) are dissolved in 30 ml of tetrahydrofuran. 11.2 ml of 1.6M solution of n-butyl lithium in hexane are added thereto in nitrogen atmosphere at -70.degree. C. for 15 minutes. The mixture is stirred at the same temperature for 30 minutes. A solution of 2.62 g of 3,4-dimethoxybenzaldehyde in 30 ml of tetrahydrofuran are added thereto for 5 minutes. After stirring the mixture for one hour at the same temperature, the mixture is gradually warmed to -10.degree. C. The mixture is poured into a mixture of 100 ml of ethyl acetate and 100 ml of water to quench the reaction. The organic layer is separated, washed with water, dried and evaporated to remove the solvent, whereby 2-(.alpha.-hydroxy-3,4-dimethoxybenzyl)-3,5-dimethoxy-4-benzyloxybenzaldehyde dimethylacetal is obtained as pale yellow syrup.
(4) 2.27 g of dimethyl acetylenedicarboxylate and 6.4 ml of acetic acid are added to the syrup obtained in paragraph (3), and the mixture is refluxed with heating for 4 hours. The reaction mixture is cooled and 100 ml of methanol are added thereto, and precipitates are collected by filtration, whereby 5.1 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,8-dimethoxy-7-benzyloxynaphthalene are obtained as colorless crystals.
M.p. 199.degree.-200.degree. C.
NMR (CDCl.sub.3, .delta.): 3.26 (s, 3H), 3.47 (s, 3H), 3.82 (s, 6H), 3.91 (s, 3H), 3.99 (s, 3H), 5.06 (s, 2H), 6.81 (s, 3H), 7.2-7.6 (m, 5H), 7.65 (s, 1H), 12.29 (s, 1H)
EXAMPLE 42
4.19 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,8-dimethoxy-7-benzyloxynaphthalene are dissolved in a mixture of 100 ml of tetrahydrofuran, 50 ml of dioxane and 50 ml of ethanol under heating. 2 g of palladium-charcoal are added thereto and the mixture is subjected to catalytic reduction in hydrogen gas at 3 atmospheric pressure for 4 hours. After the reaction, insoluble materials are filtered off and the filtrate is condensed under reduced pressure to dryness. Methanol is added to the residue and precipitates are collected by filtration, whereby 2.3 g of 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4,7-dihydroxy-6,8-dimethoxynaphthalene are obtained as colorless crystals.
M.p. 200.degree.-202.degree. C.
NMR (CDCl.sub.3, .delta.): 3.22 (s, 3H), 3.5 (s, 3H), 3.83 (s, 3H), 3.91 (s, 6H), 4.06 (s, 3H), 6.12 (s, 1H), 6.81 (s, 2H), 6.88 (s, 1H), 7.69 (s, 1H), 12.30 (s, 1H)
EXAMPLE 43
2-bromo-3-hydroxy-4,5-dimethoxybenzaldehyde, benzyl bromide, 3,4-dimethoxybenzaldehyde and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 41, whereby 1-(3,4-dimethoxyphenyl)-2,3-bis (methoxycarbonyl)-4-hydroxy-6,7-dimethoxy-8-benzyloxynaphthalene is obtained.
M.p. 196.degree.-197.degree. C.
NMR (CDCl.sub.3, .delta.): 3.43 (s, 3H), 3.73 (s, 3H), 3.75 (s, 3H), 3.83 (s, 3H), 3.90 (s, 3H), 4.02 (s, 3H), 4.55 (s, 2H), 6.5-7.4 (m, 8H), 7.70 (s, 1H), 12.30 (s, 1H)
EXAMPLE 44
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6,7-dimethoxy-8-benzyloxynaphthalene is treated in the same manner as described in Example 42, whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4,8-dihydroxy-6,7-dimethoxynapthalen 1/2dioxane is obtained as yellow prisms.
M.p. 204.degree. C.
NMR (CDCl.sub.3, .delta.): 3.48 (s, 3H), 3.66 (s, 4H, dioxane), 3.82 (s, 3H), 3.86 (s, 3H), 3.90 (s, 6H), 4.00 (s, 3H), 6.08 (s, 1H), 6.86 (s, 3H), 7.49 (s, 1H), 12.27 (s, 1H)
EXAMPLE 45
2-bromo-5-hydroxy-3,4-dimethoxybenzaldehyde, benzyl bromide, 3,4-dimethoxybenzaldehyde and dimethyl acetylenedicarboxylate are reacted in the same manner as described in Example 41, whereby 1-(3,4-dimethoxyphenyl)-2,3-bis (methoxycarbonyl)-4-hydroxy-6-benzyloxy-7,8-dimethoxynaphthalene is obtained.
M.p. 180.degree.-181.degree. C.
NMR (CDCl.sub.3, .delta.): 3.27 (s, 3H), 3.47 (s, 3H), 3.84 (s, 3H), 3.91 (s, 6H), 3.92 (s, 3H), 5.28 (s, 2H), 6.87 (s, 3H), 7.2-7.5 (m, 5H), 7.76 (s, 1H), 12.38 (s, 1H)
EXAMPLE 46
1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4-hydroxy-6-benzyloxy-7,8-dimethoxynaphthalene is treated in the same manner as described in Example 42, whereby 1-(3,4-dimethoxyphenyl)-2,3-bis(methoxycarbonyl)-4,6-dihydroxy-7,8-dimethoxynaphthalene 1/2dioxane is obtained as colorless crystals.
M.p. 179.degree. C.
NMR (CDCl.sub.3, .delta.): 3.24 (s, 3H), 3.50 (s, 3H), 3.72 (s, 4H, dioxane), 3.84 (s, 3H), 3.91 (s, 3H), 3.93 (s, 6H), 6.68 (s, 1H), 6.84 (s, 3H), 7.73 (s, 1H), 12.27 (s, 1H)
The foregoing description of the specific embodiments will so fully reveal the general nature of the invention that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and therefore such adaptations and modifications are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology and terminology employed herein is for the purpose of description and not of limitation.

Naphthalene derivatives and composition and methods of use, and aldehyde intermediates

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Klemn et al., J. Org. Chem., 27, 519-526 (1962).
Doss et al., CA, 95:80536d (1981).
Iwao et al., CA, 101:192026n (1984).
Iwao, Masatomo et al., (1984), "Generation and Diels-Adler Reaction of 1-Siloxy-3-Arylisobenzofurans from 3-Arylphthalides", Chemistry Letters, pp. 1263-1266.