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US 4,307,016 AGranted
Demethyl maytansinoids
AssigneeTakeda Chemical Industries, Ltd.
InventorsMitsuko Asai, Kazuo Nakahama, Motowo Izawa
Life of this patent
Estimating the term…
Abstract
Novel demethylmaytansinoids representable by the formula: ##STR1## [wherein X is Cl or H; R.sub.1 is H or acyl group] are produced from maytansinoids by means of enzymic transformation. The demethylmaytansinoids are useful as antifungal, antiprotozoal or antitumor agents.
Claims53
A demethylmaytansinoid compound of the formula:
- ##STR22## wherein X is Cl or H;
- R.sub.1 is H or an acyl group, the acyl group being represented by one of the formulae:
- --CO--R.sub.2 (a)
- wherein R.sub.2 is hydrogen, C.sub.1-18 alkyl, C.sub.2-18 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, phenyl, a heterocyclic group selected from the class consisting of azetidinyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 1,2,3,4-tetrahydropyridyl, piperidyl, quinolyl, 1,2-dihydroquinolyl, 3-isoquinolyl, 4-isoquinolyl, 1,2-dihydroisoquinolyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, indolyl, furyl, pyranyl, dihydropyranyl, benzofuryl, benzopyranyl, thienyl, benzothienyl, imidazolyl, pyrazolyl, pyrazinyl, pyrimidinyl, pyridazinyl, 2-imidazolyl, imidazolidinyl, benzoimidazolyl, indazolyl, quinoxalkyl, quinazolinyl, cinnolinyl, 1,4-dioxanyl, 1,4-benzodioxanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, 1,3-dithianyl, isooxazolyl, oxazolyl, morpholinyl, benzoisoxazolyl, benzoxazolyl, isothiazolyl, thiazolyl, benzoisothiazolyl, benzothiazolyl, benzothiazinyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, 1,3,5-triazinyl, benzotriazolyl, and 1,2,3,4,-tetrazolyl, said cycloalkyl, cycloalkenyl, phenyl or heterocyclic group being attached directly to the carbonyl carbon or through a C.sub.1-4 alkylene chain, said alkyl, alkenyl, cycloalkyl, cycloalkenyl, phenyl or heterocyclic group being unsubstituted or substituted by C.sub.1-4 alkoxy, C.sub.2-4 alkanoyl, C.sub.2-4 alkanoyloxy, C.sub.2-4 alkoxycarbonyl, halogen, nitro, cyano, trifluoromethyl, di-C.sub.1-4 -alkylamino, C.sub.1-4 alkylthio, methylsulfinyl, methylsulfonyl, oxo, thioxo or C.sub.1-4 alkanoylamido, and said cycloalkyl, cycloalkenyl, phenyl or heterocyclic group being unsubstituted or substituted by C.sub.1-4 alkyl;
- ##STR23## wherein R.sub.3 is hydrogen, C.sub.1-8 alkyl, C.sub.3-10 cycloalkyl, phenyl, indolyl, or imidazolyl group, said cycloalkyl, phenyl, indolyl or imidazolyl groups being attached directly to the alpha-carbon atom or through a C.sub.1-4 alkylene chain, said alkyl, cycloalkyl, phenyl, indolyl or imidazolyl being unsubstituted or substituted by C.sub.1-4 alkoxy, C.sub.2-4 alkanoyl, C.sub.2-4 alkanyloxy, C.sub.2-4 alkoxycarbonyl, halogen, nitro, cyano, trifluoromethyl, di-C.sub.1-4 alkylamino, C.sub.1-4 alkylthio, methyl- sulfinyl, methylsulfonyl, oxo, thioxo or C.sub.1-4 alkanoylamido, and said cycloalkyl, phenyl, indolyl or imidazolyl being unsubstituted or substituted by C.sub.1-4 alkyl;
- R.sub.4 is hydrogen, C.sub.1-18 alkyl, C.sub.3-10 cycloalkyl, C.sub.4-14 cycloalkylalkyl, phenyl or benzyl group, said alkyl, cycloalkyl, cycloalkylalkyl, phenyl or benzyl group being unsubstituted or substituted by C.sub.1-4 alkoxy, C.sub.2-4 alkanoyl, C.sub.2-4 alkanoyloxy, C.sub.2-4 alkoxycarbonyl, halogen, nitro, cyano, trifluoromethyl, di-C.sub.1-4 -alkylamino, C.sub.1-4 alkylthio, methylsulfinyl, methylsulfonyl, oxo, thioxo or C.sub.1-4 alkanoylamido, and said cycloalkyl, cycloalkylalkyl, phenyl or benzyl group being unsubstituted or substituted by C.sub.1-4 alkyl;
- R.sub.5 is hydrogen, C.sub.1-7 alkoxy, bornyloxy, isobornyloxy, benzyloxy, C.sub.1-18 alkyl, C.sub.2-18 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, phenyl or a heterocyclic group selected from the class consisting of azetidinyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 1,2,3,4-tetrahydropyridyl, piperidyl, quinolyl, 1,2-dihydroquinolyl, 3-isoquinolyl, 4-isoquinolyl, 1,2-dihydroisoquinolyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, indolyl, furyl, pyranyl, dihydropyranyl, benzofuryl, benzopyranyl, thienyl, benzothienyl, imidazolyl, pyrazolyl, pyrazinyl, pyrimidinyl, pyridazinyl, 2-imidazolyl, imidazolidinyl, benzoimidazolyl, indazolyl, quinoxalyl, quinozolinyl, cinnolinyl, 1,4-dioxanyl, 1,4-benzodioxanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, 1,3-dithianyl, isooxazolyl, oxazolyl, morpholinyl, benzoisoxazolyl, benzoxazolyl, isothiazolyl, thiazolyl, benzoisothiazolyl, benzothiazolyl, benzothiazinyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, 1,3,5-triazinyl, benzotriazolyl and 1,2,3,4-tetrazolyl, said cycloalkyl, cycloalkenyl, phenyl or heterocyclic groups being attached directly to the carbonyl carbon atom adjacent the nitrogen atom or through a C.sub.1-4 alkylene chain, said alkyl, alkenyl, cycloalkyl, cycloalkenyl, phenyl or heterocyclic group being unsubstituted or substituted by C.sub.1-4 alkoxy, C.sub.2-4 alkanoyl, C.sub.2-4 alkanoyloxy, C.sub.2-4 alkoxycarbonyl, halogen, nitro, cyano, trifluoromethyl, di-C.sub.1-4 -alkylamino, C.sub.1-4 alkylthio, methylsulfinyl, methylsulfonyl, oxo, thioxo or C.sub.1-4 alkanoylamido, and said cycloalkyl, cycloalkenyl, phenyl or heterocyclic group being unsubstituted or substituted by C.sub.1-4 alkyl;
- ##STR24## wherein R.sub.6 and R.sub.7 may be the same or different and each is hydrogen, C.sub.1-18 alkyl, C.sub.2-18 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, C.sub.4-14 cycloalkylalkyl, C.sub.4-10 cycloalkenylalkyl, phenyl, phenyl-C.sub.1-14 alkyl, phenyl-C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkylphenyl, biphenyl or heterocyclic group selected from the class consisting of azetidinyl, pyrrolyl, furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isooxazolyl, pyrazolyl, imidazolyl, pyridyl, pyrimidinyl, pyrazinyl, triazinyl, quinolyl, quinazolyl, quinoxalyl, indolyl, benzofuranyl and benzothienyl, and wherein R.sub.6 and R.sub.7 together may form a heterocyclic group of azetidinyl, pyrrolidinyl, piperidinyl or morpholinyl taken together with the adjacent nitrogen atom, these groups being unsubstituted or substituted by C.sub.1-4 alkoxy, C.sub.1-4 alkylthio, phenoxy, phenylthio, cyclohexyloxy, halogen, cyano, C.sub.2-5 alkoxycarbonyl, benzyloxycarbonyl, nitro, aminosulfonyl, or di-C.sub.1-4 -alkylamino, and said cyclic moiety or heterocyclic group being unsubstituted or substituted by C.sub.1-4 alkyl;
- or
- --CO--O--R.sub.8 (d)
- wherein R.sub.8 is C.sub.1-18 alkyl, C.sub.3-10 cycloalkyl, phenyl or phenyl-C.sub.1-4 -alkyl, said groups being unsubstituted or substituted by C.sub.1-4 alkoxy, phenoxy, benzyloxy, halogen or cyano, and said cyclic moiety being unsubstituted or substituted by C.sub.1-4 alkyl, C.sub.3-10 -cycloalkyl, C.sub.3-10 -cycloalkenyl or phenyl.
8 more elements
Dependencies are inferred from the claim text.