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US 7,427,390 B2Granted
Radiohalogenated benzamide derivatives and their use in tumor diagnosis and tumor therapy
AssigneeSchering Corporation
InventorsMatthias Friebe, Peter Muschick, Andreas Huth
Life of this patent
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Abstract
This invention relates to new radiohalogenated benzamide derivatives and their use in tumor diagnosis and tumor therapy. The radiohalogenated benzamide derivatives according to the invention exhibit novel and especially advantageous properties, in particular with respect to tumor concentration and retardation, liver concentration and blood accumulation. The radiation-therapy doses to be achieved in the tumor, compared to healthy body tissue, are advantageous for the compounds according to the invention.
Claims29
A radiohalogenated benzamide compound of formula (I),
- in which
- X1 to X5 are, each independently of one another, halogen, hydrogen, —NR1R2, —O—R3, a branched or unbranched C1-C10 alkyl group, a branched or unbranched C2-C10 alkenyl group or an aryl or heteroaryl group that is optionally substituted by halogen or alkoxy, wherein two adjacent radicals X1 to X5 can form a 5- to 7-membered ring, wherein one or more carbon atoms of the ring can be replaced by heteroatoms,
- X6 is an oxygen or NH,
- X7 and X8 can be the same or different and are hydrogen, C1-12 alkyl, C2-12 alkenyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C2-6 carbalkoxyalkyl, C2-6 carbalkoxyalkenyl, C6-12 aryl or C6-12 heteroaryl;
- in each case optionally substituted in one or more places by OR4, COOR5, CONR6R7, cyano, halogen or NR8R9, or
- X7 and X8 together form a 5- to 7-membered ring, wherein one or more carbons of the ring can be replaced by heteroatoms,
- R1 and R2 are the same or different and are hydrogen, C1-12 alkyl, C2-12 alkenyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C2-6 carboxyalkyl, C2-6 carboxyalkenyl, C1-12 alkyl, C6-12 arylsulfonyl, carboxyaryl, in particular C7-13 carboxyaryl, carboxy heteroaryl;
- in each case optionally substituted in one or more places by aryl, heteroaryl, OR4, COOR5, CONR6R7, cyano, halogen or NR8R9, or two substituents taken together form a 3, 4, 5, 6, 7 or 8 membered ring, optionally with 1, 2, 3, or 4 hetero atoms, provided that R1 and R2 cannot simultaneously be hydrogen,
- R3 is hydrogen, C6-12 aryl, heteroaryl, C1-10 alkyl, C2-10 alkenyl, C2-10 alkinyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, in each case optionally substituted in one or more places by OR4, COOR5, CONR6R7, cyano, halogen or NR8R9,
- R4 and R5 are the same or different and are hydrogen, C1-12 alky, C2-12 alkenyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, optionally substituted in one or more places by aryl, heteroaryl, OR10, COOR11, CONR6R7, cyano, halogen or NR8R9,
- R6, R7,
- R8 and R9 are the same or different and are hydrogen, C1-12 alkyl, C2-12 alkenyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, in each case optionally substituted in one or more places by OR4, or
- R6 and R7 or
- R8 and R9 in each case together form a 5- to 7-membered ring, wherein one or more carbons of the ring can be replaced by heteroatoms, and
- R10, R11 are the same or different and are hydrogen, C1-12 alkyl, C2-12 alkenyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, which are optionally substituted in each case in one or more places by aryl, heteroaryl, OR4, COOR5, CONR6R7, cyano, halogen, or NR8R9,
- provided that
- at least one of radicals X1 to X5 is a radioactive halogen,
- at least one of radicals X1 to X5 is —O—R3,
- at least one of radicals X1 to X5 is a radical of formula —NR1R2, in which either R1 or R2 is a substituted or unsubstituted carboxyalkyl, carboxyalkenyl carboxyaryl or carboxyheteroaryl, and
- if X1 is methoxy, X6 is O, X8 is hydrogen, X7 is NH(CH2)2NEt2, and X4 means I131, X3 is not NHAc,
- or a pharmaceutically acceptable salt thereof.
18 more elements
Dependencies are inferred from the claim text.