WO1998005624A1 - Composes amino et agonistes du recepteur de l'angiotensine iv - Google Patents
Composes amino et agonistes du recepteur de l'angiotensine iv Download PDFInfo
- Publication number
- WO1998005624A1 WO1998005624A1 PCT/JP1997/002716 JP9702716W WO9805624A1 WO 1998005624 A1 WO1998005624 A1 WO 1998005624A1 JP 9702716 W JP9702716 W JP 9702716W WO 9805624 A1 WO9805624 A1 WO 9805624A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- pharmaceutically acceptable
- amino compound
- acceptable salt
- angiotensin
- Prior art date
Links
- 239000000018 receptor agonist Substances 0.000 title claims abstract description 6
- 229940044601 receptor agonist Drugs 0.000 title claims abstract description 6
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- 125000004998 naphthylethyl group Chemical group C1(=CC=CC2=CC=CC=C12)CC* 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 229940074439 potassium sodium tartrate Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000005495 pyridazyl group Chemical group 0.000 description 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- 125000005030 pyridylthio group Chemical group N1=C(C=CC=C1)S* 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000036454 renin-angiotensin system Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 210000000329 smooth muscle myocyte Anatomy 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- SDKPSXWGRWWLKR-UHFFFAOYSA-M sodium;9,10-dioxoanthracene-1-sulfonate Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S(=O)(=O)[O-] SDKPSXWGRWWLKR-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- YJAAJMSZVZJPOQ-DTWKUNHWSA-N tert-butyl n-[(2s,3s)-3-methyl-1-oxopentan-2-yl]carbamate Chemical compound CC[C@H](C)[C@@H](C=O)NC(=O)OC(C)(C)C YJAAJMSZVZJPOQ-DTWKUNHWSA-N 0.000 description 1
- YKTZLYCYDQJXRH-JKIKYLSZSA-N tert-butyl n-[(e,3s)-5-methyl-1-naphthalen-1-ylhex-1-en-3-yl]carbamate Chemical compound C1=CC=C2C(/C=C/[C@@H](NC(=O)OC(C)(C)C)CC(C)C)=CC=CC2=C1 YKTZLYCYDQJXRH-JKIKYLSZSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical class C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- WOPGHMKDMNSLIR-UHFFFAOYSA-M triphenyl(2-phenylethyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1CC[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WOPGHMKDMNSLIR-UHFFFAOYSA-M 0.000 description 1
- UGDYRTOUNGDPDN-UHFFFAOYSA-M triphenyl(pyridin-4-ylmethyl)phosphanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=NC=C1 UGDYRTOUNGDPDN-UHFFFAOYSA-M 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108700043117 vasectrin I Proteins 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
Definitions
- the present invention relates to an amino compound useful as a medicament, and more particularly to an amino compound useful as a therapeutic agent for various conditions in which angiotensin IV is involved.
- the renin-angiotensin system is a cascade of enzymatic peptide splitting that produces peptides involved in coronary vessels and electrolyte homeostasis.
- This cascade begins when renin converts angiotensinogen to a physiologically inactive angiotensin I, which is then converted to angiotensin ⁇ , and then to angiotensin HI, and furthermore to hexane. It is converted to the peptide angiotensin IV.
- the receptor for angiotensin IV is distributed at low concentrations in various organ tissues such as brain (particularly hippocampus), adrenal gland, heart, kidney, smooth muscle cells, and endothelial cells.
- This angiotensin IV has, for example, a renal blood flow-increasing effect (Swansoti, et al., Regulatory Pepti des, 1992, 40, 409.), a cerebral vasodilator effect (Haberl, et al., Circ. Res., 1991, 68). , 1621.), cytostatic activity (Barker and Aceto, Am. J. Physio., 1990, 259, H610.), Memory-enhancing activity (Millering, et al., J. Pharmacol. Exp. , 1993, 266, 1718).
- the present inventors have developed amino compounds that act at low concentrations on the angiotensin IV receptor. As a result of intensive studies for the purpose of providing, the present inventors have found that a specific amino compound strongly acts on angiotensin IV receptor, and have completed the present invention. That is, the present invention provides the following general formula (1) 1 R-
- X represents CH 2 NH or CONH
- Y represents CH 2 NH or CONH
- R ′ represents a hydrogen atom or an S-substituted or unsubstituted “lower alkyl group, cycloalkyl group, cycloalkyl-substituted alkyl group
- R 2 and R : i independently represent a substituted or unsubstituted lower alkyl or aralkyl group;
- R 4 and R 5 independently represent a hydrogen atom or a substituted or Represents an unsubstituted “alkyl group, aralkyl group, aryl group or heteroaryl group”, or a pharmaceutically acceptable salt thereof.
- the present invention also provides a drug comprising the amino compound represented by the above general formula (1) or a pharmaceutically acceptable salt thereof,
- An alkoxycarbonyl group is C 2 -C,. And specific examples thereof include, for example, methoxycarbonyl, ethoxycarbonyl, propyloxycarbonyl, aryloxycarbonyl, benzyloxycarbonyl and the like. it can.
- the lower alkyl group C means a straight-chain or branched alkyl group -C beta, specific examples of the unsubstituted lower alkyl groups such as methyl group, Echiru group, a propyl group, I an isopropyl group, a butyl group , Isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, tertopentyl, 1-methylbutyl, 2-methylbutyl, 1,2-dimethylpropyl, hexyl , Isohexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 1,1-dimethyl Butyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl.
- alkyl group a C 1 to C 12 linear or branched alkyl group is preferable.
- the unmodified product include the above-mentioned lower alkyl group, heptyl group, octyl group, nonyl group, decyl group, Dodecyl groups and their iso-, sec- and tert-forms.
- the alkenyl group is preferably a C 6 -C 6 linear or branched alkenyl group, and specific examples of the unsubstituted compound include, for example, a vinyl group, an aryl group, a 1-propenyl group, a 1-butenyl group, a 2- Butenyl group, 3-butenyl group, 2-methyl-1-propenyl group, 2-methyl-2-propenyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 3 -Methyl-1-butenyl group, 3-methyl-2-butenyl group, 3-methyl-3-butenyl group, 2-methyl-1-butenyl group, 2-methyl-2-butenyl group, 2-methyl-3- Butenyl, 2-ethyl-2-propenyl, 1-methyl-1-butenyl, 1-methyl-2-butenyl, 1-methyl-3-butenyl, 1-hexenyl, 2-to Xeny
- a cycloalkyl group C 3 to CS as the cycloalkyl group, specific examples of the non-location recombinants, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, heptyl group cycloalkyl, Shikurookuchiru group Is mentioned.
- C 4 -C as the cycloalkyl substituted alkyl group.
- non-substituted product examples include, for example, cyclomethyl pyrmethyl group, cyclopropylbutyl group, cyclobutylpropyl group, cyclopentylethyl group, cyclohexylmethyl group, cycloheptylmethyl group, cyclooctylethyl And the like.
- the aralkyl group means an alkyl group substituted by an aralkyl group including a heteroaryl group, and specific examples of the unsubstituted compound include, for example, a benzyl group, a phenethyl group, a phenylpropyl group, a phenylbutyl group, and a naphthylmethyl group.
- the aryl group also includes a heteroaryl group, and specific examples of the unsubstituted group include, for example, a phenyl group, a naphthyl group, a biphenyl group, an anthranyl group, a pyrrolyl group, a furyl group, a phenyl group, and an imidazolyl group.
- substituents which may be present in the above groups include a halogen atom such as a chlorine atom, a bromine atom, an iodine atom and a fluorine atom; a nitro group: a hydroxyyl group; a formyl group; a carbonyl group; a cyano group; A methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a 1-methylbutyl group, 2-methylbutyl, 1,2-dimethylpropyl, hexyl, isohexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 1,1-dimethylbut
- amino compounds represented by the above general formula (1) of the present invention an amino compound in which X is CH 2 NH is preferable in view of its strong activity, and among them, an amino compound in which Y is CONH is preferred. Particularly preferred.
- X is CH 2 NH and R 1 and R 3 are substituted or unsubstituted “lower alkyl” because of its strong activity.
- R 3 a represents.
- a substituted or unsubstituted lower alkyl group amino compound is preferably represented by.
- R la is a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, An amino compound which is a group selected from the group consisting of -methylthioethyl group is preferred.
- the amino compound of the present invention represented by the general formula (1) can form a pharmaceutically acceptable salt.
- a salt include, when an acidic group is present, a gold salt such as a lithium salt, a sodium salt, a potassium salt, a magnesium salt, and a calcium salt, or an ammonium salt, a methyl ammonium salt, and a dimethyl ammonium salt.
- Ammonium salts such as trimethylammonium salt, tetramethylammonium salt, dicyclohexylammonium salt and the like. If a basic group is present, hydrochloride, bromate, sulfate, Minerates such as nitrates and phosphates, or methanesulfonate, benzenesulfonate, p-toluenesulfonate, acetate, propionate, tartrate, fumarate, maleate, apple Organic acid salts such as acid, oxalate, succinate, citrate, benzoate, mandelate, lactate and trifluoroacetate It can be mentioned.
- the stereochemistry of the asymmetric carbon present in the amino compound represented by the general formula (1) can be independently (R), (S) or (RS), and
- the stereochemistry at the double bond site can be in (E), (Z) or (EZ) form.
- the amino compound can be produced, for example, by the following method.
- R 'R 5 are as defined above, A 1 and A 3 represents a protecting group of the Amino group, A 2 represents a protecting group of carboxyl group.
- the amino acid (b) is reacted with the aldehyde (a), and then the amino compound (c) is obtained by a reduction reaction. Further, a protecting group is introduced into the amino group, and hydrolysis is performed to obtain a carboxylic acid (e).
- the aldehyde (f) is reacted with an ylide (g) to obtain an alkene (h>. Then, the protective group of the argen isomer (h) is removed), and the condensing agent is used. After reacting the carboxylic acid (e), the amino-protecting group is removed to produce the amino compound (1a) of the present invention. Further, the amino compound (la) of the present invention can be produced by reducing the amino compound (la).
- an amino acid (1) is reacted with an aldehyde (k) obtained by reduction of a dipeptide (j), and then treated with a reducing agent-3 to obtain an amino form (m).
- the amino compound (1b) of the present invention can be produced by removing the protecting group of the amino group of the amino compound (m).
- the amino form (o) is obtained by reacting the aldehyde form (a ') with the amino form U), followed by treatment with the reducing agent-1.
- the amino-protecting group of the amino form (o) is removed to obtain (P), and then the amino acid is reacted with a condensing agent, and then the amino-protecting group is removed.
- the amino compound (1c) of the invention can be produced.
- the amino compound (1c ′) of the present invention can be produced by reducing the amino compound (1c).
- the ester form (d) is reacted with a reducing agent-3, then the amino form (i), and then treated with a reducing agent-1 to obtain a diamino form (q).
- a reducing agent-3 By removing the protecting group of the amino group of the diamino compound (Q), the amino compound (1d) of the present invention can be produced.
- the amino compound (1d ') of the present invention can be produced by treating the amino compound (1d) with the reducing agent-2.
- reducing agent-1 for example, a metal hydride compound such as sodium cyanoborohydride, lithium cyanoborohydride, sodium borohydride, lithium aluminum hydride or dimethylamine -Polan complex can be used.
- the amount of reducing agent-1 used is about 1 to 5 equivalents.
- Reducing agent-2 means a catalytic hydrogenation reaction in the presence of a catalyst.
- the catalyst for example, palladium, palladium-black, palladium-carbon, platinum, platinum oxide, rhodium and the like can be used, and the use amount of about 0.001 to 1 equivalent is sufficient.
- reducing agent-3 for example, diisobutylaluminum hydride, sodium aluminum hydride, tritert-butoxyaluminum hydride and the like can be used.
- the amount of reducing agent-3 used is about 1 to 5 equivalents.
- Solvents used in the reactions using these reducing agents include aromatic hydrocarbons such as toluene and benzene, tetrahydrofuran, dioxane, getyl ether, and diisopropane.
- Ethers such as propyl ether, halogenated hydrocarbons such as dichloromethane, dichloroethane, and chloroform, methanol, ethanol, water, a mixed solvent thereof, and any solvent that does not participate in the reaction can be used.
- the reaction temperature is between 178T and 200T, and the reaction time is about 0.5-24 hours.
- the protecting group for the amino group includes benzyloxycarbonyl, tert-butoxycarbonyl, formyl, chloroacetyl, trityl, trialkylsilyl, acetamidomethyl, benzyl, 9 -A group that can be easily removed by acid hydrolysis or hydrogenolysis such as fluorenylmethoxycarbonyl group can be used, and as a protecting group for carboxyl group, methyl group, ethyl group, benzyl group, phenacyl group can be used. Etc. can be used.
- Reagents and methods used for the condensation reaction in the above-mentioned production method include N- ⁇ '-dicyclohexylcarbodiimide and 1-hydroxybenzotriazo- along with ⁇ , ⁇ '-dicyclohexylcarbodiimide.
- Soptyl, diphenylphosphorylazide and the like can be mentioned as suitable reagents and methods.
- Removal of the protecting group can be carried out according to the method described in the literature, by adding a mineral acid such as hydrogen fluoride, hydrochloric acid, or hydrogen bromide, an organic acid such as trifluoroacetic acid, or a hydroxylic acid such as sodium hydroxide or barium hydroxide. Decomposition, hydrogen reduction in the presence of a palladium metal compound, etc.
- a mineral acid such as hydrogen fluoride, hydrochloric acid, or hydrogen bromide
- an organic acid such as trifluoroacetic acid
- a hydroxylic acid such as sodium hydroxide or barium hydroxide.
- Aromatic hydrocarbons such as ethers, benzene, and toluene; halogenated hydrocarbons such as dichloromethane and dichloroethane , Non-protonic polar solvents such as dimethyl sulfoxide, ⁇ , ⁇ -dimethylformamide, etc., and mixed solvents thereof, as well as any solvents that do not participate in the reaction. .
- the reaction temperature is preferably from 180 to 20O: in particular, from 130 to 50X for the condensation reaction, and from 130 to 100X for the removal of the protecting group. In the reaction, -78 to 50 is preferred.
- N- (tert-butoxycarbonyl) -L-norleucine methyl ester (10.7 g, 38 ⁇ 1) was dissolved in toluene (68 ml) and cooled to -78 :. While keeping the solution at ⁇ 60 to ⁇ 70, diisobutylaluminum hydride (toluene 1.0 M solution, 51 ml) was slowly added. After stirring at -78 for 1 hour, the cooling bath was removed, and methanol (2 ml) was added.
- tyrosine methyl ester hydrochloride (13.6 g, 59 mmol) and acetic acid (3.5 g, 59 miD01) were dissolved in methanol (69 m) -tetrahydrofuran (98 ml) and added. Further, a turbid solution of tetrahydrofuran (30 ml) of sodium cyanoborohydride (2.7, 43minol) was added. After stirring at room temperature for 2.5 hours, water was added. The solid was removed by decantation, and the solution was concentrated under reduced pressure. The organic matter was extracted with ethyl acetate, and washed sequentially with a saturated aqueous solution of sodium hydrogen carbonate, water and saturated saline.
- reaction solution was poured into ice water, extracted with ethyl acetate, and washed sequentially with water and brine.
- the solution was concentrated under reduced pressure, and the residue was purified by column chromatography (3S, 4S)-(E) -N- (tert-butoxycarponyl) -4
- N- (tert-butoxycarbonyl) -L-leucine methyl ester (0.98 g, 4. OiniDol) was dissolved in toluene (7.1 ml) and cooled to -78. While maintaining the reaction solution at ⁇ 60 to ⁇ 70 :, diisobutylaluminum hydride (a 1.0 M solution in toluene, 5.0 ml) was slowly added to the solution. The mixture was further stirred at -78 for 30 minutes to prepare (S) -2- (tert-butoxycarbonylamino) -4-methylpentanal.
- N- (tert-Butoxycarbonyl)-(L) -leucine methyl ester (9.8 g, 40 mmol) was dissolved in toluene (70 ml) under an argon stream and cooled to -78. While maintaining -60X: to -70X :, diisobutylaluminum hydride (toluene 1.0M solution, 52ml) was slowly added to the solution. After stirring at -78 for 40 minutes, the cooling bath was removed, and methanol (2. lml) and an aqueous solution of 20% citric acid (30 inl) were added.
- Reference Example 2 (4-Pyridylmethyl) triphenylphosphonium chloride was prepared in the same manner as in (2) and (3), and 2- (tert-butoxycarbonylamino) -4-synthesized in the same manner as in Reference Example 2 (1). The title compound was obtained from methylpentanal.
- Angiotensin IV receptor binding ability was determined using a Hartley guinea pig hippocampus and described in Mi 11 er-Wing et a, J. Pharmacol. Exp. Ther., Vol. 266, ppl 718 (1993). It measured according to.
- the guinea-pig hippocampus of the first strain was purified from 5 OmM Tris-HCl containing ImM ethylenediamine ⁇ , ⁇ , ⁇ ', N'-tetraacetic acid (EDTA) and 100 ⁇ phenylmethanesulfonylfluoride (PMS F). Homogenized with buffer (pH 7.4). The cells were separated at 900 ⁇ g and the obtained supernatant was centrifuged at 48,000 ⁇ g. After washing the sediment once with the same buffer, the sediment was washed with 5 OmM Tris containing 15 OmM sodium chloride, 1 mM EDTA, 100 ⁇ M PMS F, 0.1% ⁇ serum albumin (BSA). The protein was suspended in a hydrochloric acid buffer (pH 7.4) so that the protein concentration was 50 g / m 1, to obtain a crude membrane sample.
- EDTA ImM ethylenediamine ⁇ , ⁇ , ⁇ ', N'-tetra
- the obtained membrane sample was reacted with a test compound dissolved in 0.2 nM 12s I-angiotensin IV and dimethyl sulfoxide at 37 "for 90 minutes to give 125 I-angiotensin IV bound to the membrane.
- Suction filtration was performed on GF / B filter paper using a cell harvester for binding experiments, and the radioactivity on the filter paper was measured using a gamma counter.Non-specific binding was determined in the presence of 1 M angiotensin IV. The binding was calculated by subtracting the nonspecific binding from the total binding.
- the receptor binding ability ( IC5C value) of the test compound was determined by comparing the concentration of the test compound with 0.2 nM 125 I-angiotensin IV at a different concentration. The concentration was determined as the concentration of the test compound that inhibited binding by 50% from the inhibition curve obtained by the reaction. Are shown in Table 1, Table 1
- novel amino compound of the present invention is useful as a medicament, and in particular, acts on angiotensin IV receptor, so that various disease states involving angiotensin IV, such as renal blood flow increasing action, cerebral vasodilator action, cells It is useful as a therapeutic agent (antagonist or agonist) for antiproliferative action, memory effect, etc.
- the compound of the present invention is added with a conventional bulking agent, a binder, a disintegrant, a pH adjuster, a solubilizing agent, and the like, and the tablet, pill, capsule, It can be prepared into granules, powders, solutions, emulsions, suspensions, injections and the like.
- the compound of the present invention can be administered orally or parenterally to an adult patient in a dose of 0.0130 mg once or several times a day. This dose can be adjusted appropriately according to the type of disease, age, weight, and symptoms of the patient.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97933908A EP0882699A4 (en) | 1996-08-06 | 1997-08-05 | AMINO CONNECTIONS AND ANGIOTENSIN IV RECEPTOR AGONISTS |
AU37090/97A AU714295B2 (en) | 1996-08-06 | 1997-08-05 | Amino compounds and angiotensin IV receptor agonists |
CA002242571A CA2242571C (en) | 1996-08-06 | 1997-08-05 | Amino compounds and angiotensin iv receptor agonists |
US09/101,449 US6066672A (en) | 1996-08-06 | 1997-08-05 | Amino compounds and angiotensin IV receptor agonists |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8/207010 | 1996-08-06 | ||
JP20701096 | 1996-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998005624A1 true WO1998005624A1 (fr) | 1998-02-12 |
Family
ID=16532705
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1997/002716 WO1998005624A1 (fr) | 1996-08-06 | 1997-08-05 | Composes amino et agonistes du recepteur de l'angiotensine iv |
Country Status (5)
Country | Link |
---|---|
US (1) | US6066672A (ja) |
EP (1) | EP0882699A4 (ja) |
AU (1) | AU714295B2 (ja) |
CA (1) | CA2242571C (ja) |
WO (1) | WO1998005624A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013040208A (ja) * | 2005-04-12 | 2013-02-28 | Vicore Pharma Ab | 新規な三環系アンジオテンシンiiアゴニスト |
JP2013063995A (ja) * | 2005-04-12 | 2013-04-11 | Vicore Pharma Ab | 新規な三環系アンジオテンシンiiアゴニスト |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003011304A1 (en) * | 2001-08-02 | 2003-02-13 | Howard Florey Institute Of Experimental Physiology And Medicine | Modulation of insulin-regulated aminopeptidase (irap)/angiotensin iv (at4) receptor activity |
US20070023336A1 (en) * | 2005-08-01 | 2007-02-01 | Owens Kevin M | Inline filter monitoring device |
WO2023099589A1 (en) | 2021-12-01 | 2023-06-08 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Irap inhibitors for use in the treatment of inflammatory diseases |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994000492A1 (en) * | 1992-06-24 | 1994-01-06 | Washington State University Research Foundation | Angiotensin iv peptides and receptor |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2036397C (en) * | 1990-02-23 | 2000-12-12 | Paul Cates Anderson | Hiv protease inhibitors containing derived amino acid units |
IE20010533A1 (en) * | 1990-11-20 | 2003-03-05 | Abbott Lab | Intermediates for preparing retroviral protease inhibiting compounds |
JP3429338B2 (ja) * | 1992-07-27 | 2003-07-22 | 杏林製薬株式会社 | 新規なアリールグリシンアミド誘導体及びその製造法 |
GB2276618A (en) * | 1993-03-29 | 1994-10-05 | Merck & Co Inc | Inhibitors of isoprenylated protein endoprotease |
KR19990028753A (ko) * | 1995-07-07 | 1999-04-15 | 곤도 기요시 | 펩티드 유도체 및 안지오텐신 iv 수용체 작동약 |
-
1997
- 1997-08-05 US US09/101,449 patent/US6066672A/en not_active Expired - Fee Related
- 1997-08-05 CA CA002242571A patent/CA2242571C/en not_active Expired - Fee Related
- 1997-08-05 EP EP97933908A patent/EP0882699A4/en not_active Withdrawn
- 1997-08-05 WO PCT/JP1997/002716 patent/WO1998005624A1/ja not_active Application Discontinuation
- 1997-08-05 AU AU37090/97A patent/AU714295B2/en not_active Ceased
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994000492A1 (en) * | 1992-06-24 | 1994-01-06 | Washington State University Research Foundation | Angiotensin iv peptides and receptor |
Non-Patent Citations (7)
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013040208A (ja) * | 2005-04-12 | 2013-02-28 | Vicore Pharma Ab | 新規な三環系アンジオテンシンiiアゴニスト |
JP2013063995A (ja) * | 2005-04-12 | 2013-04-11 | Vicore Pharma Ab | 新規な三環系アンジオテンシンiiアゴニスト |
Also Published As
Publication number | Publication date |
---|---|
AU714295B2 (en) | 1999-12-23 |
CA2242571A1 (en) | 1998-02-12 |
AU3709097A (en) | 1998-02-25 |
EP0882699A4 (en) | 2001-03-21 |
EP0882699A1 (en) | 1998-12-09 |
US6066672A (en) | 2000-05-23 |
CA2242571C (en) | 2006-05-16 |
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