JP2011502147A5 - - Google Patents

Info

Publication number

JP2011502147A5

JP2011502147A5 JP2010532037A JP2010532037A JP2011502147A5 JP 2011502147 A5 JP2011502147 A5 JP 2011502147A5 JP 2010532037 A JP2010532037 A JP 2010532037A JP 2010532037 A JP2010532037 A JP 2010532037A JP 2011502147 A5 JP2011502147 A5 JP 2011502147A5

Authority

JP

Japan

Prior art keywords

compound

formula

pharmaceutical composition

base

contacting

Prior art date

2008-10-28

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
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• 150000001875 compounds Chemical class 0.000 claims 17
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 9
• 239000008194 pharmaceutical composition Substances 0.000 claims 7
• 239000002798 polar solvent Substances 0.000 claims 5
• 229940126062 Compound A Drugs 0.000 claims 4
• NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 4
• SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 4
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical group [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
• LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical group [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 claims 3
• 150000003839 salts Chemical class 0.000 claims 3
• 239000012453 solvate Substances 0.000 claims 3
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 3
• 206010028980 Neoplasm Diseases 0.000 claims 2
• 239000002207 metabolite Substances 0.000 claims 2
• 229910000027 potassium carbonate Inorganic materials 0.000 claims 2
• DNISYQIZVIFCRA-UHFFFAOYSA-N 4-(1-aminoethyl)-2,6-ditert-butylphenol Chemical compound CC(N)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 DNISYQIZVIFCRA-UHFFFAOYSA-N 0.000 claims 1
• QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
• 206010027476 Metastases Diseases 0.000 claims 1
• 239000002671 adjuvant Substances 0.000 claims 1
• 230000033115 angiogenesis Effects 0.000 claims 1
• 239000003085 diluting agent Substances 0.000 claims 1
• 239000003814 drug Substances 0.000 claims 1
• 125000001072 heteroaryl group Chemical group 0.000 claims 1
• 230000009401 metastasis Effects 0.000 claims 1
• 239000000203 mixture Substances 0.000 claims 1
• 125000003107 substituted aryl group Chemical group 0.000 claims 1
• 229940124597 therapeutic agent Drugs 0.000 claims 1
• 230000004614 tumor growth Effects 0.000 claims 1
• DTMFCPVMRRFMQE-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1OCC2)ccc1N2C(Nc1n[o]c(CO)c1)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1OCC2)ccc1N2C(Nc1n[o]c(CO)c1)=O DTMFCPVMRRFMQE-UHFFFAOYSA-N 0.000 description 1
• 0 Cc1cc(NC(N(CCOc2c3)c2ccc3Oc2c(cc(*)c(OC)c3)c3ncc2)=*)n[o]1 Chemical compound Cc1cc(NC(N(CCOc2c3)c2ccc3Oc2c(cc(*)c(OC)c3)c3ncc2)=*)n[o]1 0.000 description 1
• DOKTUYMPPOUFNS-UHFFFAOYSA-N Cc1cc(NC(N(CCOc2c3)c2ccc3Oc2c(cc(c(O)c3)OC)c3ncc2)=O)n[o]1 Chemical compound Cc1cc(NC(N(CCOc2c3)c2ccc3Oc2c(cc(c(O)c3)OC)c3ncc2)=O)n[o]1 DOKTUYMPPOUFNS-UHFFFAOYSA-N 0.000 description 1
• QIIPQYDSKRYMFG-UHFFFAOYSA-N OC(Oc1ccccc1)=O Chemical compound OC(Oc1ccccc1)=O QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 1