KR880013926A - 복소환식 케톤 - Google Patents

복소환식 케톤 Download PDF

Info

Publication number
KR880013926A
KR880013926A KR1019880005474A KR880005474A KR880013926A KR 880013926 A KR880013926 A KR 880013926A KR 1019880005474 A KR1019880005474 A KR 1019880005474A KR 880005474 A KR880005474 A KR 880005474A KR 880013926 A KR880013926 A KR 880013926A
Authority
KR
South Korea
Prior art keywords
group
alkyl
trifluoromethyl
alkoxy
halogeno
Prior art date
Application number
KR1019880005474A
Other languages
English (en)
Inventor
필립 듀크 에드워드
조세프 제임스 루이스
찰스 윌리암 퍼킨스
다이안 아미 트레이너
리차드 알랜 윌돈저
Original Assignee
원본미기재
아이씨아이 아메리카스 아이엔씨
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from GB878711050A external-priority patent/GB8711050D0/en
Priority claimed from GB888803206A external-priority patent/GB8803206D0/en
Application filed by 원본미기재, 아이씨아이 아메리카스 아이엔씨 filed Critical 원본미기재
Publication of KR880013926A publication Critical patent/KR880013926A/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06034Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
    • C07K5/06052Val-amino acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06191Dipeptides containing heteroatoms different from O, S, or N

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음

Description

복소환식 케톤
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (1)

  1. 식 1의 화합물 및 그것의 제약학적으로 허용가능한 염기-부가 염.
    식중, -Q-는 (ⅰ) 할로게노, 니트로, -NRgRh의 아미노 그룹, -NHCORm의 아실아미노 그룹, 하이드록시, -OCORn의 아실옥시 그룹, (1-4c)알콕시, (1-4c)알킬, 트리플루오로메틸, 카복시, 시아노, 〔(1-4c)알콕시〕카보닐, -CONRpRq(Rp=Rq일대 -CONRp 2포함)의 아미노카보닐 그룹, 설포, SO2NRiRj의 설폰아미도 및 (1-3c)하이드록시알킬로 구성되는 그룹에서 독립적으로 선택된 하나 또는 두 개의 치환제를 임으로 가지는 오르토-페닐렌 ; 및 (ⅱ) -C(Ra)=C(Rb)의 시스-비닐렌 그룹으로 구성되는 그룹에서 선택 ; Ra및 Rb는 수소, 니트로, -NRgRh의 아미노 그룹, -OCORn의 아실옥시 그룹, (1-4c)알콕시, (r6c)알킬, 트리플루오로메틸, 카복시, 시아노, 〔(1-4c)알콕시〕카보닐, -CONRpRq(Rp=Rq일대 -CONRp 2포함)의 아미노카보닐 그룹, 하이드록시메틸 그룹 및 할로게노, 니트로, (1-4c)알콕시, (1-4c)알킬 및 트리플루오로메틸로 구성되는 그룹에서 선태된 하나 또는 두 개의 치환제를 임의로 가지는 페닐로 구성되는 구릅에서 각각 독립적으로 선택; Rg, Rh, Ri, Rj, Rm, Rp및 Rq는 각각 수소 및(1-4c)알킬로 구성되는 그룹에서 독립적으로 선택; Rn은 (1-4c)알킬, X는 산소 및 황으로 구성되는 그룹에서 선택; A는 -CO-, -NH.CO- 및 -O.CO-로 구성되는 그룹에서 선택; L은 알켄디일의이중결합에 또는 페닐렌알킬 그룹의 임의 이중결합내에 포함된 탄소가 그룹A의 질소 또는 산소 원자에 직접적으로 결합되지 않는 조건으로, 알킬 부분내에 하나의 이중 결합을 임으로 포함하는, 페닐렌, (1-6c)알칸디일, (2-6c)알켄디일 및 페닐렌(1-3c)알킬로 구성되는 그룹에서 선택; R4는 R5, S(O2).NH.CO-의 아실설폰아미드, R5.CO.NH.S(O2)-의 아실설폰아미드, R5.NH.CO.NH.S(O2)-의 설포닐우레아, R5.S(O2).NH.CO.NR6-의 설포닐우레아 및 CF3.S(O2).NH-의 트리플루오로메틸설폰아미드로 구성되는 그룹에서 선택; R5는 (1-10c)알킬; 트리플루오로메틸; (3-10c)사이클로알킬; 할로게노, 니트로, 아미노, 디메틸아미노, 하이드록시, 메틸, 트리플루오로메틸, 카복시, 페닐 및 〔(1-5c) 알킬카보닐〕아미노로 구성되는 그룹의 1-3개로 임의 치환된 (6 또는 10c)아릴; 및 방향족계의 탄소 3개까지가 할로게노 및 트리플루오로메틸로 구성되는 그룹에서 독립적으로 선택된 치환체를 가질 수 있는 방향족 복소환식 그룹으로 구성되는 그룹에서 선택; R6은 수소 또는 메틸.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880005474A 1987-05-11 1988-05-11 복소환식 케톤 KR880013926A (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB8711050 1987-05-11
GB878711050A GB8711050D0 (en) 1987-05-11 1987-05-11 Selected heterocyclic ketones
GB8803206 1988-02-11
GB888803206A GB8803206D0 (en) 1988-02-11 1988-02-11 Selected heterocyclic ketones

Publications (1)

Publication Number Publication Date
KR880013926A true KR880013926A (ko) 1988-12-22

Family

ID=26292230

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019880005474A KR880013926A (ko) 1987-05-11 1988-05-11 복소환식 케톤

Country Status (22)

Country Link
US (1) US5164371A (ko)
EP (1) EP0291234B1 (ko)
JP (1) JPS6445395A (ko)
KR (1) KR880013926A (ko)
CN (1) CN1037519A (ko)
AT (1) ATE103293T1 (ko)
AU (1) AU605284B2 (ko)
CA (1) CA1326107C (ko)
DE (1) DE3888568T2 (ko)
DK (1) DK260588A (ko)
ES (1) ES2063034T3 (ko)
FI (1) FI91072C (ko)
GB (1) GB8809316D0 (ko)
HU (1) HU201963B (ko)
IE (1) IE62524B1 (ko)
IL (1) IL86236A (ko)
NO (1) NO176519C (ko)
NZ (1) NZ224452A (ko)
PT (1) PT87454B (ko)
SU (1) SU1678207A3 (ko)
ZA (1) ZA883006B (ko)
ZW (1) ZW4988A1 (ko)

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8910550D0 (en) * 1989-05-08 1989-06-21 Ici America Inc Substituted amides
GB8910547D0 (en) * 1989-05-08 1989-06-21 Ici America Inc Substituted ketones
DK0458537T3 (da) * 1990-05-24 1999-10-18 Zeneca Ltd Anvendelse af en terapeutisk forbindelse til behandling af bronkitis
US5162348A (en) * 1990-05-24 1992-11-10 Imperial Chemical Industries Plc Treatment of cystic fibrosis
DK0458536T3 (da) * 1990-05-24 1998-10-19 Zeneca Ltd Terapeutisk middel til behandling og forebyggelse af åndedrætsbesværsyndrom hos voksne
EP0475531B1 (en) * 1990-09-10 1995-01-18 Asahi Kasei Kogyo Kabushiki Kaisha Benzoic acid phenylester compounds and elastase inhibiting compositions containing the same
US6159938A (en) * 1994-11-21 2000-12-12 Cortech, Inc. Serine protease inhibitors comprising α-keto heterocycles
US6001811A (en) * 1994-11-21 1999-12-14 Cortech Inc. Serine protease inhibitors--N-substituted derivatives
US6150334A (en) * 1994-11-21 2000-11-21 Cortech, Inc. Serine protease inhibitors-tripeptoid analogs
US6015791A (en) * 1994-11-21 2000-01-18 Cortech Inc. Serine protease inhibitors-cycloheptane derivatives
US6001814A (en) * 1994-11-21 1999-12-14 Cortech Inc. Serine protease inhibitors
US6001813A (en) * 1994-11-21 1999-12-14 Cortech Inc. Val-pro containing α-keto oxadiazoles as serine protease inhibitors
US6100238A (en) * 1994-11-21 2000-08-08 Cortech Inc. Indole and tetrahydroisoquinoline containing Alpha-keto oxadiazoles as serine protease inhibitors
US5998379A (en) * 1994-11-21 1999-12-07 Cortech Inc. Serine protease inhibitors-proline analogs
US5618792A (en) * 1994-11-21 1997-04-08 Cortech, Inc. Substituted heterocyclic compounds useful as inhibitors of (serine proteases) human neutrophil elastase
US20020119985A1 (en) 1994-11-21 2002-08-29 Albert Gyorkos Serine protease inhibitors
US5556990A (en) * 1994-12-16 1996-09-17 Rhone-Poulenc Rorer Pharmaceuticals Inc. Polyarylcarbamoylaza- and -carbamoylalkanedioic acids
US5804560A (en) * 1995-01-06 1998-09-08 Sibia Neurosciences, Inc. Peptide and peptide analog protease inhibitors
US6017887A (en) * 1995-01-06 2000-01-25 Sibia Neurosciences, Inc. Peptide, peptide analog and amino acid analog protease inhibitors
US6369080B2 (en) 1996-10-11 2002-04-09 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6194435B1 (en) 1996-10-11 2001-02-27 Cor Therapeutics, Inc. Lactams as selective factor Xa inhibitors
US6063794A (en) 1996-10-11 2000-05-16 Cor Therapeutics Inc. Selective factor Xa inhibitors
US6262047B1 (en) 1996-10-11 2001-07-17 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6133256A (en) * 1997-04-14 2000-10-17 Cor Therapeutics Inc Selective factor Xa inhibitors
AU6896298A (en) 1997-04-14 1998-11-11 Cor Therapeutics, Inc. Selective factor xa inhibitors
AU6896398A (en) 1997-04-14 1998-11-11 Cor Therapeutics, Inc. Selective factor xa inhibitors
US6274602B1 (en) * 1998-06-03 2001-08-14 Gpi Nil Holdings, Inc. Heterocyclic thioester and ketone hair growth compositions and uses
US6333321B1 (en) 1997-08-11 2001-12-25 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6218382B1 (en) 1997-08-11 2001-04-17 Cor Therapeutics, Inc Selective factor Xa inhibitors
US6228854B1 (en) 1997-08-11 2001-05-08 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6177572B1 (en) * 1997-08-20 2001-01-23 Sepracor, Inc. Solid and liquid-phase synthesis of benzoxazoles and benzothiazoles and their use
US6656910B2 (en) 1997-12-04 2003-12-02 Cortech, Inc. Serine protease inhibitors
US6184377B1 (en) 1997-12-15 2001-02-06 Sepracor Inc. Compositions containing N-amino- and N-hydroxy-quinazolinones and methods for preparing libraries thereof
AU4415899A (en) 1998-06-03 1999-12-20 Cortech, Inc. Alpha-keto oxadiazoles as serine protease inhibitors
JP2000256396A (ja) 1999-03-03 2000-09-19 Dainippon Pharmaceut Co Ltd 複素環式化合物およびその中間体ならびにエラスターゼ阻害剤
TW200404789A (en) 1999-03-15 2004-04-01 Axys Pharm Inc Novel compounds and compositions as protease inhibitors
EP1169311A4 (en) * 1999-03-22 2004-09-15 Rhode Island Education COMBINATORIAL OXAZOLE AND THIAZOLE BANKS
WO2000078812A1 (en) * 1999-06-17 2000-12-28 Source Precision Medicine, Inc. Method and compounds for inhibiting activity of serine elastases
US7030116B2 (en) 2000-12-22 2006-04-18 Aventis Pharmaceuticals Inc. Compounds and compositions as cathepsin inhibitors
US7064123B1 (en) 2000-12-22 2006-06-20 Aventis Pharmaceuticals Inc. Compounds and compositions as cathepsin inhibitors
RS19504A (en) 2001-09-14 2007-02-05 Aventis Pharmaceuticals Inc., Novel compounds and compositions as cathepsin inhibitors
HUP0401906A3 (en) 2001-11-14 2008-07-28 Aventis Pharma Inc Novel cathepsin s inhibitors, process for their preparation and pharmaceutical compositions containing them
JP2005526830A (ja) * 2002-04-16 2005-09-08 アクシス・ファーマシューティカルズ・インコーポレイテッド ヘテロアリール及び不飽和ヘテロシクロアルキルマグネシウム試薬の製造方法及び使用
JP3744890B2 (ja) 2002-11-01 2006-02-15 ハッピー工業株式会社 ミシン
DE102004045648A1 (de) * 2004-09-21 2006-03-23 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Betamimetika zur Behandlung von Atemwegserkrankungen
CA2651762A1 (en) 2006-05-23 2007-11-29 Irm Llc Compounds and compositions as channel activating protease inhibitors
EP2099454A4 (en) * 2006-11-17 2010-11-10 Abbott Lab AMINOPYRROLIDINES AS CHEMOKINE RECEPTOR ANTAGONISTS
MX2009008518A (es) 2007-02-09 2009-08-20 Irm Llc Compuestos y composiciones como inhibidores de la proteasa activadora de canal.
FR2914920B1 (fr) 2007-04-11 2011-09-09 Clariant Specialty Fine Chem F Procede de deacetalisation d'alpha-aminoacetals.
FR2916441B1 (fr) 2007-05-22 2009-08-28 Clariant Specialty Fine Chem Procede de racemisation d'alpha-aminoacetals optiquement actifs.
WO2009007415A2 (en) * 2007-07-10 2009-01-15 Probiodrug Ag Novel compounds
US20090156509A1 (en) * 2007-12-12 2009-06-18 Accuthera, Inc. Tri-peptide Inhibitors of Serine Elastases
FR2927900B1 (fr) 2008-02-27 2010-09-17 Clariant Specialty Fine Chem Procede de preparation d'alpha-aminoacetals optiquement actifs.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3481913D1 (de) * 1983-04-27 1990-05-17 Ici America Inc Prolin-derivate.
US4643991A (en) * 1984-12-18 1987-02-17 The University Of Kentucky Research Foundation Peptide elastase inhibitors and methods
GB8600263D0 (en) * 1985-01-22 1986-02-12 Ici America Inc Peptide derivatives
DE3683541D1 (de) * 1985-06-07 1992-03-05 Ici America Inc Selektionierte difluorverbindungen.
EP0368449A3 (en) * 1988-09-09 1991-08-14 George Alexander Digenis Elastase inhibiting polymers and methods to produce them
GB8910547D0 (en) * 1989-05-08 1989-06-21 Ici America Inc Substituted ketones

Also Published As

Publication number Publication date
IE62524B1 (en) 1995-02-08
DE3888568D1 (de) 1994-04-28
AU1539088A (en) 1988-11-17
DK260588A (da) 1988-11-12
PT87454B (pt) 1992-08-31
NO882036L (no) 1988-11-14
FI882176A0 (fi) 1988-05-10
ZW4988A1 (en) 1989-12-06
DE3888568T2 (de) 1994-07-21
NZ224452A (en) 1991-06-25
FI91072C (fi) 1994-05-10
EP0291234A3 (en) 1990-08-22
CA1326107C (en) 1994-01-11
NO176519C (no) 1995-04-19
SU1678207A3 (ru) 1991-09-15
CN1037519A (zh) 1989-11-29
JPS6445395A (en) 1989-02-17
AU605284B2 (en) 1991-01-10
NO176519B (no) 1995-01-09
IL86236A (en) 1994-12-29
ES2063034T3 (es) 1995-01-01
GB8809316D0 (en) 1988-05-25
PT87454A (pt) 1989-05-31
HUT46708A (en) 1988-11-28
EP0291234B1 (en) 1994-03-23
HU201963B (en) 1991-01-28
DK260588D0 (da) 1988-05-11
NO882036D0 (no) 1988-05-10
EP0291234A2 (en) 1988-11-17
FI882176A (fi) 1988-11-12
ATE103293T1 (de) 1994-04-15
US5164371A (en) 1992-11-17
FI91072B (fi) 1994-01-31
ZA883006B (ko) 1988-11-11
IL86236A0 (en) 1988-11-15
IE881416L (en) 1988-11-11

Similar Documents

Publication Publication Date Title
KR880013926A (ko) 복소환식 케톤
ES2147223T3 (es) Derivados de indol como agonistas de tipo 5-ht1.
CA2250840A1 (en) Antivirally active heterocyclic azahexane derivatives
KR930004276A (ko) 치환된 헤테로사이클류
BR9807132A (pt) Derivados de pirrolidina tendo atividade inibitória de fosfolipase a2
KR880013909A (ko) 고혈압 치료 화합물에 대한 테트라졸 중간체
DK1031563T3 (da) Sulfonylderivater
HUP0302337A2 (hu) Pirimidin-2,4,6-trion metalloproteáz inhibitorok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
KR950032570A (ko) 액정 화합물 및 액정 조성물.
FI914476A (fi) Tricykliska heterocykliska foereningar.
DE59203014D1 (de) Haftvermittler.
ES2172580T3 (es) 1,3-oxatiolanos sustituidos con propiedades antiviricas.
FR2673427B1 (fr) Derives heterocycliques diazotes n-substitues par un groupement biphenylmethyle, leur preparation, les compositions pharmaceutiques en contenant.
DE69217312D1 (de) Tricyclische Heterocyclen als PGE2-Antagonisten
EP0671390A3 (en) Antithrombotic agents
KR900006331A (ko) 항미생물성 퀴놀로닐 락탐
KR900006347A (ko) 살균성 플루오로퀴놀로닐 세펨
FR2665441B1 (fr) Derives de la n-sulfonyl indoline, leur preparation, les compositions pharmaceutiques en contenant.
KR880005104A (ko) 제 초 제
KR890009867A (ko) 비 펩타이드성 레닌 억제제
ATE190842T1 (de) Arzneizusammensetzungen enthaltend argatrobananaloge
DE59710874D1 (de) Schwefel enthaltende heterocyclische Bradykinin-Antagonisten, Verfahren zu ihrer Herstellung und ihre Verwendung
KR960703599A (ko) 항전이제로 사용되는 세펨 유도체의 용도(use of cephem derivatives as anti-metastatic agents)
IT1206498B (it) Derivati amidinici del4-fenilmidazolo 2-sostituto processi per la loro preparazione e loro uso farmaceutico.
KR910700244A (ko) 테트라알킬피페리디닐-치환된 우라실 유도체 및 이의 자외선 안정화제로서의 용도

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
SUBM Surrender of laid-open application requested