ES2279009T3 - Derivados de lactama como antagonistas de receptores 11cby humanos. - Google Patents

Info

Publication number

ES2279009T3

ES2279009T3 ES02801693T ES02801693T ES2279009T3 ES 2279009 T3 ES2279009 T3 ES 2279009T3 ES 02801693 T ES02801693 T ES 02801693T ES 02801693 T ES02801693 T ES 02801693T ES 2279009 T3 ES2279009 T3 ES 2279009T3

Authority

ES

Spain

Prior art keywords

group

formula

compound

phenyl

ring

Prior art date

2001-10-15

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.)

Expired - Lifetime

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• 239000005557 antagonist Substances 0.000 title description 10
• 150000001875 compounds Chemical class 0.000 claims abstract description 247
• -1 methoxymethoxy Chemical group 0.000 claims abstract description 61
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 40
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 29
• 150000003839 salts Chemical class 0.000 claims abstract description 27
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 24
• 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 23
• 125000003118 aryl group Chemical group 0.000 claims abstract description 19
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 16
• 229910052760 oxygen Inorganic materials 0.000 claims abstract description 16
• 125000001424 substituent group Chemical group 0.000 claims abstract description 16
• 239000001257 hydrogen Substances 0.000 claims abstract description 15
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
• 229910052717 sulfur Inorganic materials 0.000 claims abstract description 14
• 125000002619 bicyclic group Chemical group 0.000 claims abstract description 12
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 12
• 239000012453 solvate Substances 0.000 claims abstract description 12
• 125000005843 halogen group Chemical group 0.000 claims abstract description 11
• 125000002618 bicyclic heterocycle group Chemical group 0.000 claims abstract description 10
• 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 10
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 8
• 125000005842 heteroatom Chemical group 0.000 claims abstract description 7
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 6
• 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 6
• 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims abstract description 6
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 6
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 6
• 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 5
• 125000002947 alkylene group Chemical group 0.000 claims abstract description 5
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 5
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims abstract description 5
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 4
• 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 4
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 4
• 238000000034 method Methods 0.000 claims description 84
• 239000002253 acid Substances 0.000 claims description 41
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 40
• 239000002904 solvent Substances 0.000 claims description 39
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 23
• 150000001412 amines Chemical class 0.000 claims description 22
• 238000011282 treatment Methods 0.000 claims description 21
• 150000008064 anhydrides Chemical class 0.000 claims description 18
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 15
• 125000004429 atom Chemical group 0.000 claims description 13
• UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 13
• 125000003545 alkoxy group Chemical group 0.000 claims description 12
• 101800002739 Melanin-concentrating hormone Proteins 0.000 claims description 11
• 239000002585 base Substances 0.000 claims description 11
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
• 208000008589 Obesity Diseases 0.000 claims description 8
• 239000003054 catalyst Substances 0.000 claims description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
• 235000020824 obesity Nutrition 0.000 claims description 8
• QMNWYGTWTXOQTP-UHFFFAOYSA-N 1h-triazin-6-one Chemical compound O=C1C=CN=NN1 QMNWYGTWTXOQTP-UHFFFAOYSA-N 0.000 claims description 7
• 239000000010 aprotic solvent Substances 0.000 claims description 7
• 206010012601 diabetes mellitus Diseases 0.000 claims description 7
• VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical group OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 7
• 239000003795 chemical substances by application Substances 0.000 claims description 6
• 150000003949 imides Chemical class 0.000 claims description 6
• 229910052763 palladium Inorganic materials 0.000 claims description 6
• 208000019901 Anxiety disease Diseases 0.000 claims description 5
• 208000020925 Bipolar disease Diseases 0.000 claims description 5
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 5
• 230000005856 abnormality Effects 0.000 claims description 5
• 230000036506 anxiety Effects 0.000 claims description 5
• 229910052736 halogen Inorganic materials 0.000 claims description 5
• 238000010438 heat treatment Methods 0.000 claims description 5
• 239000008194 pharmaceutical composition Substances 0.000 claims description 5
• KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 claims description 4
• 125000004414 alkyl thio group Chemical group 0.000 claims description 4
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
• 208000028683 bipolar I disease Diseases 0.000 claims description 4
• 239000003814 drug Substances 0.000 claims description 4
• 239000001301 oxygen Substances 0.000 claims description 4
• XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 4
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
• 201000000980 schizophrenia Diseases 0.000 claims description 4
• CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 4
• 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 3
• YCIPQJTZJGUXND-UHFFFAOYSA-N Aglaia odorata Alkaloid Natural products C1=CC(OC)=CC=C1C1(C(C=2C(=O)N3CCCC3=NC=22)C=3C=CC=CC=3)C2(O)C2=C(OC)C=C(OC)C=C2O1 YCIPQJTZJGUXND-UHFFFAOYSA-N 0.000 claims description 3
• 208000031886 HIV Infections Diseases 0.000 claims description 3
• 239000007868 Raney catalyst Substances 0.000 claims description 3
• NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims description 3
• 229910000564 Raney nickel Inorganic materials 0.000 claims description 3
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
• 229910000102 alkali metal hydride Inorganic materials 0.000 claims description 3
• 150000008046 alkali metal hydrides Chemical class 0.000 claims description 3
• 125000003342 alkenyl group Chemical group 0.000 claims description 3
• 201000010099 disease Diseases 0.000 claims description 3
• 208000015181 infectious disease Diseases 0.000 claims description 3
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
• 208000024714 major depressive disease Diseases 0.000 claims description 3
• 238000004519 manufacturing process Methods 0.000 claims description 3
• 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
• 239000011593 sulfur Substances 0.000 claims description 3
• 230000001225 therapeutic effect Effects 0.000 claims description 3
• 238000002560 therapeutic procedure Methods 0.000 claims description 3
• 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 3
• 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims description 2
• KEIFWROAQVVDBN-UHFFFAOYSA-N 1,2-dihydronaphthalene Chemical compound C1=CC=C2C=CCCC2=C1 KEIFWROAQVVDBN-UHFFFAOYSA-N 0.000 claims description 2
• QMNUDYFKZYBWQX-UHFFFAOYSA-N 1H-quinazolin-4-one Chemical compound C1=CC=C2C(=O)N=CNC2=C1 QMNUDYFKZYBWQX-UHFFFAOYSA-N 0.000 claims description 2
• PZMKGWRBZNOIPQ-UHFFFAOYSA-N 1h-thieno[3,2-d]pyrimidin-4-one Chemical compound OC1=NC=NC2=C1SC=C2 PZMKGWRBZNOIPQ-UHFFFAOYSA-N 0.000 claims description 2
• OSEVYTJMMHAQGG-UHFFFAOYSA-N 2-methylsulfanyl-1h-thieno[3,2-d]pyrimidin-4-one Chemical compound N1C(SC)=NC(=O)C2=C1C=CS2 OSEVYTJMMHAQGG-UHFFFAOYSA-N 0.000 claims description 2
• SZDUJHZOLZGLMV-UHFFFAOYSA-N 2-sulfanylidene-1h-thieno[3,2-d]pyrimidin-4-one Chemical compound O=C1NC(=S)NC2=C1SC=C2 SZDUJHZOLZGLMV-UHFFFAOYSA-N 0.000 claims description 2
• IVRCHBYBKXRNIC-UHFFFAOYSA-N 3-[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)phenyl]-6-phenylthieno[3,2-d]pyrimidin-4-one Chemical compound COC1=CC(N2C(C=3SC(=CC=3N=C2)C=2C=CC=CC=2)=O)=CC=C1OCCN1CCCC1 IVRCHBYBKXRNIC-UHFFFAOYSA-N 0.000 claims description 2
• JEDVKUHCDPPWNR-UHFFFAOYSA-N 3h-thieno[2,3-d]pyrimidin-4-one Chemical compound O=C1NC=NC2=C1C=CS2 JEDVKUHCDPPWNR-UHFFFAOYSA-N 0.000 claims description 2
• 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 2
• 206010002383 Angina Pectoris Diseases 0.000 claims description 2
• 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 2
• 208000032841 Bulimia Diseases 0.000 claims description 2
• 206010006550 Bulimia nervosa Diseases 0.000 claims description 2
• 206010007556 Cardiac failure acute Diseases 0.000 claims description 2
• 206010007559 Cardiac failure congestive Diseases 0.000 claims description 2
• 206010012218 Delirium Diseases 0.000 claims description 2
• 206010012289 Dementia Diseases 0.000 claims description 2
• 208000012661 Dyskinesia Diseases 0.000 claims description 2
• 206010019280 Heart failures Diseases 0.000 claims description 2
• 241000713340 Human immunodeficiency virus 2 Species 0.000 claims description 2
• 208000023105 Huntington disease Diseases 0.000 claims description 2
• 206010020751 Hypersensitivity Diseases 0.000 claims description 2
• 206010020772 Hypertension Diseases 0.000 claims description 2
• 206010028980 Neoplasm Diseases 0.000 claims description 2
• 208000012902 Nervous system disease Diseases 0.000 claims description 2
• 208000025966 Neurological disease Diseases 0.000 claims description 2
• 208000001132 Osteoporosis Diseases 0.000 claims description 2
• 208000002193 Pain Diseases 0.000 claims description 2
• 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 2
• 208000028017 Psychotic disease Diseases 0.000 claims description 2
• 208000036623 Severe mental retardation Diseases 0.000 claims description 2
• 238000006069 Suzuki reaction reaction Methods 0.000 claims description 2
• 208000025865 Ulcer Diseases 0.000 claims description 2
• ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 claims description 2
• 206010046555 Urinary retention Diseases 0.000 claims description 2
• 230000001154 acute effect Effects 0.000 claims description 2
• 230000007815 allergy Effects 0.000 claims description 2
• 208000022531 anorexia Diseases 0.000 claims description 2
• 150000001543 aryl boronic acids Chemical class 0.000 claims description 2
• 208000006673 asthma Diseases 0.000 claims description 2
• 230000001580 bacterial effect Effects 0.000 claims description 2
• BNBQRQQYDMDJAH-UHFFFAOYSA-N benzodioxan Chemical compound C1=CC=C2OCCOC2=C1 BNBQRQQYDMDJAH-UHFFFAOYSA-N 0.000 claims description 2
• 238000009835 boiling Methods 0.000 claims description 2
• 239000003153 chemical reaction reagent Substances 0.000 claims description 2
• 206010061428 decreased appetite Diseases 0.000 claims description 2
• 230000002538 fungal effect Effects 0.000 claims description 2
• 201000001421 hyperglycemia Diseases 0.000 claims description 2
• PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 claims description 2
• 208000010125 myocardial infarction Diseases 0.000 claims description 2
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
• 238000007363 ring formation reaction Methods 0.000 claims description 2
• 208000019116 sleep disease Diseases 0.000 claims description 2
• 231100000397 ulcer Toxicity 0.000 claims description 2
• 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
• 241000713772 Human immunodeficiency virus 1 Species 0.000 claims 1
• 208000016620 Tourette disease Diseases 0.000 claims 1
• 150000001350 alkyl halides Chemical class 0.000 claims 1
• 230000021523 carboxylation Effects 0.000 claims 1
• 238000006473 carboxylation reaction Methods 0.000 claims 1
• 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
• 238000006193 diazotization reaction Methods 0.000 claims 1
• 238000006073 displacement reaction Methods 0.000 claims 1
• 230000004927 fusion Effects 0.000 claims 1
• 210000002816 gill Anatomy 0.000 claims 1
• 201000004240 prostatic hypertrophy Diseases 0.000 claims 1
• 239000003586 protic polar solvent Substances 0.000 claims 1
• 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
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• 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 10
• 125000005330 8 membered heterocyclic group Chemical group 0.000 abstract description 2
• 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 3
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
• 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 1
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 152
• 239000000203 mixture Substances 0.000 description 102
• 238000005160 1H NMR spectroscopy Methods 0.000 description 79
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 62
• 239000000243 solution Substances 0.000 description 56
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 40
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 38
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 37
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 36
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 33
• 239000000463 material Substances 0.000 description 31
• 239000007787 solid Substances 0.000 description 31
• VFRSADQPWYCXDG-LEUCUCNGSA-N ethyl (2s,5s)-5-methylpyrrolidine-2-carboxylate;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.CCOC(=O)[C@@H]1CC[C@H](C)N1 VFRSADQPWYCXDG-LEUCUCNGSA-N 0.000 description 30
• 238000003818 flash chromatography Methods 0.000 description 30
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 26
• 239000003921 oil Substances 0.000 description 24
• 235000019198 oils Nutrition 0.000 description 24
• 239000000741 silica gel Substances 0.000 description 24
• 229910002027 silica gel Inorganic materials 0.000 description 24
• RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 24
• WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 22
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 19
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
• XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 18
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 18
• 229910000041 hydrogen chloride Inorganic materials 0.000 description 18
• DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 17
• 239000012074 organic phase Substances 0.000 description 16
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 15
• HYTACLVSJIFYBY-UHFFFAOYSA-N azane;dichloromethane;methanol Chemical compound N.OC.ClCCl HYTACLVSJIFYBY-UHFFFAOYSA-N 0.000 description 15
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 14
• 239000000706 filtrate Substances 0.000 description 14
• CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 14
• 238000006243 chemical reaction Methods 0.000 description 13
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 12
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 11
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 11
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 11
• VBPMITJBSXBGOI-UHFFFAOYSA-N 3-methoxy-4-(2-pyrrolidin-1-ylethoxy)aniline Chemical compound COC1=CC(N)=CC=C1OCCN1CCCC1 VBPMITJBSXBGOI-UHFFFAOYSA-N 0.000 description 10
• YQYKTRBWNKDCFR-UHFFFAOYSA-N 4-[2-[di(propan-2-yl)amino]ethoxy]-3-methoxyaniline Chemical compound COC1=CC(N)=CC=C1OCCN(C(C)C)C(C)C YQYKTRBWNKDCFR-UHFFFAOYSA-N 0.000 description 10
• UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 10
• 239000012267 brine Substances 0.000 description 10
• ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 description 10
• 238000002360 preparation method Methods 0.000 description 10
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• CNHVHQJLWJENPY-UHFFFAOYSA-N 2-amino-n-[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)phenyl]-4-phenoxybenzamide Chemical compound C=1C=C(OCCN2CCCC2)C(OC)=CC=1NC(=O)C(C(=C1)N)=CC=C1OC1=CC=CC=C1 CNHVHQJLWJENPY-UHFFFAOYSA-N 0.000 description 9
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• 229910052786 argon Inorganic materials 0.000 description 9
• HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 9
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• 208000035475 disorder Diseases 0.000 description 8
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• DHHUCKHXSFKTAJ-UHFFFAOYSA-N 1-[2-(2-methoxy-4-nitrophenoxy)ethyl]azetidine Chemical compound COC1=CC([N+]([O-])=O)=CC=C1OCCN1CCC1 DHHUCKHXSFKTAJ-UHFFFAOYSA-N 0.000 description 7
• PZYPNBPKQPUEMB-UHFFFAOYSA-N 5-bromo-2-[4-[2-[di(propan-2-yl)amino]ethoxy]-3-methoxyphenyl]isoindole-1,3-dione Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC(N2C(C3=CC(Br)=CC=C3C2=O)=O)=C1 PZYPNBPKQPUEMB-UHFFFAOYSA-N 0.000 description 7
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• 102400001132 Melanin-concentrating hormone Human genes 0.000 description 7
• 238000004587 chromatography analysis Methods 0.000 description 7
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• 238000001914 filtration Methods 0.000 description 7
• 125000001072 heteroaryl group Chemical group 0.000 description 7
• 229910052943 magnesium sulfate Inorganic materials 0.000 description 7
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