HUP0301671A2 - 4-Fenil-piridin-származékok, mint neurokinin-1-receptor antagonisták, eljárás az előállításukra és alkalmazásuk - Google Patents
4-Fenil-piridin-származékok, mint neurokinin-1-receptor antagonisták, eljárás az előállításukra és alkalmazásukInfo
- Publication number
- HUP0301671A2 HUP0301671A2 HU0301671A HUP0301671A HUP0301671A2 HU P0301671 A2 HUP0301671 A2 HU P0301671A2 HU 0301671 A HU0301671 A HU 0301671A HU P0301671 A HUP0301671 A HU P0301671A HU P0301671 A2 HUP0301671 A2 HU P0301671A2
- Authority
- HU
- Hungary
- Prior art keywords
- group
- lower alkyl
- hydrogen atom
- optionally
- substituted
- Prior art date
Links
- 150000005362 4-phenylpyridines Chemical class 0.000 title 1
- 239000002742 neurokinin 1 receptor antagonist Substances 0.000 title 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- QDZOEBFLNHCSSF-PFFBOGFISA-N (2S)-2-[[(2R)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S)-1-[(2R)-2-amino-5-carbamimidamidopentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-N-[(2R)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]pentanediamide Chemical compound C([C@@H](C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](N)CCCNC(N)=N)C1=CC=CC=C1 QDZOEBFLNHCSSF-PFFBOGFISA-N 0.000 abstract 1
- 102100024304 Protachykinin-1 Human genes 0.000 abstract 1
- 101800003906 Substance P Proteins 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
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- 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
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- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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Abstract
A találmány (I) általános képletű vegyületekre és gyógyászatilagalkalmas savaddíciós sóikra vonatkozik. A képletben R jelentésehidrogén- vagy halogénatom; R1 jelentése -(C<C)mR1' vagy -(CR'=CR<)mR1'; ahol R1' jelentése halogénatom; cianocsoport; valamely(A) általános képletű csoport; -C(O)NR'R<; -C(O)O(CH2)mR5; -C(O)R5; -N(OH)-(CH2)mR5; -NR'C(O)-(CH2)mR5; -N[C(O)-R']2; -OR6; -(CH2)m-SR6, -(CH2)m-S(O)R6 vagy -(CH2)m-S(O)2R6; adott esetben egy vagy többszubsztituenssel helyettesített arilcsoport; vagy 5- vagy 6-tagú, egy-négy nitrogén-, oxigén- és/vagy kén-heteroatomot tartalmazóheteroaril-csoport, amely adott esetben egy vagy több szubsztituensselhelyettesítve lehet; vagy (B) általános képletű 5- vagy 6-tagútelített gyűrűs tercier amin, amely adott esetben egy továbbinitrogén-, oxigén- vagy kén-heteroatomot tartalmazhat; R5 jelentésehidrogénatom, ciano-, hidroxicsoport, halogénatom, trifluor-metilcsoport, -C(O)OR', -OC(O)R' vagy adott esetben egy vagy többszubsztituenssel helyettesített arilcsoport; vagy jelentése 5- vagy 6-tagú, egy-négy nitrogén-, oxigén- és/vagy kén-heteroatomot tartalmazóheteroaril-csoport, amely adott esetben R6 jelentése hidrogénatom, kisszénatomszámú alkil-, trifluor-metil- vagy arilcsoport, mimellett akis szénatomszámú alkil- vagy arilcsoport adott esetben helyettesítvelehet, vagy R6 jelentése 5- vagy 6-tagú, egy-négy nitrogén-, oxigén-és/vagy kén-heteroatomot tartalmazó heteroaril-csoport, amely adottesetben helyettesítve lehet; R7 jelentése -C(O)-(CH2)mOH vagyoxocsoport; R2 jelentése hidrogénatom, kis szénatomszámú alkil-, kisszénatomszámú alkoxicsoport, halogénatom vagy trifluor-metil-csoport;R3/R3' jelentése egymástól függetlenül hidrogénatom vagy kisszénatomszámú alkilcsoport; vagy R3 vagy R3' a szénatommal együtt,amelyhez kapcsolódnak, cikloalkilcsoportot képezhet; R4/R4' jelentéseegymástól függetlenül hidrogénatom, halogénatom, trifluor-metil-, kisszénatomszámú alkil- vagy kis szénatomszámú alkoxicsoport; R és R2vagy R4 és R4' együtt adott esetben egy vagy két kis szénatomszámúalkilcsoporttal, halogénatommal és/vagy kis szénatomszámúalkoxicsoporttal helyettesített -CH=CH-CH=CH- csoportot képez; Xjelentése -C(O)N(R8)-, (CH2)pO-, -(CH2)pN(R8)-, -N(R8)C(O)- vagy -N(R8)-(CH2)p-; ahol R8 jelentése hidrogénatom vagy kis szénatomszámúalkilcsoport; n értéke 1 vagy 2; m értéke 0, 1, 2, 3 vagy 4; o értéke1 vagy 2; és p értéke 1 vagy 2]. A találmány szerinti vegyületek aneurokinin 1(NK-1, P-anyag) receptor antagonistái és e receptorralösszefüggő betegségek kezelésére alkalmazhatók. A találmány kiterjed avegyületek előállítására is. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00117003 | 2000-08-08 | ||
PCT/EP2001/008686 WO2002016324A1 (en) | 2000-08-08 | 2001-07-27 | 4-phenyl-pyridine derivatives as neurokinin-1 receptor antagonists |
Publications (2)
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HUP0301671A3 HUP0301671A3 (en) | 2010-03-29 |
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HU0301671A HUP0301671A3 (en) | 2000-08-08 | 2001-07-27 | 4-phenyl-pyridine derivatives as neurokinin-1 receptor antagonists, process for their preparation and their use |
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EP (1) | EP1309559B1 (hu) |
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KR (1) | KR100518201B1 (hu) |
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AR (1) | AR030324A1 (hu) |
AT (1) | ATE328871T1 (hu) |
AU (2) | AU1211802A (hu) |
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PL (1) | PL359849A1 (hu) |
PT (1) | PT1309559E (hu) |
RU (1) | RU2277087C2 (hu) |
SI (1) | SI1309559T1 (hu) |
TW (1) | TWI259180B (hu) |
UY (1) | UY26872A1 (hu) |
WO (1) | WO2002016324A1 (hu) |
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PL2225230T3 (pl) | 2007-12-07 | 2017-08-31 | Vertex Pharmaceuticals Incorporated | Stałe postacie kwasu 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-ilo)cyklopropanokarboksyamido)-3-metylopirydyn-2-ylo)benzoesowego |
MX364936B (es) | 2007-12-07 | 2019-05-15 | Vertex Pharma | Procesos para producir acidos cicloalquilcarboxamido-piridin benzoicos. |
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FR2954315B1 (fr) * | 2009-12-23 | 2012-02-24 | Galderma Res & Dev | Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique |
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