KR970705557A - 편두통 치료제인 인돌 유도체의 염(salts of an anti-migraine indole derivative) - Google Patents

편두통 치료제인 인돌 유도체의 염(salts of an anti-migraine indole derivative) Download PDF

Info

Publication number
KR970705557A
KR970705557A KR1019970701281A KR19970701281A KR970705557A KR 970705557 A KR970705557 A KR 970705557A KR 1019970701281 A KR1019970701281 A KR 1019970701281A KR 19970701281 A KR19970701281 A KR 19970701281A KR 970705557 A KR970705557 A KR 970705557A
Authority
KR
South Korea
Prior art keywords
compound
formula
suitable solvent
pharmaceutical composition
disease
Prior art date
Application number
KR1019970701281A
Other languages
English (en)
Other versions
KR100228952B1 (ko
Inventor
발레리에 데니스 하딩
로스 제임스 마크라에
로날드 제임스 오길비에
Original Assignee
무어 제임스 더블유
화이자 리서치 앤드 디벨롭먼트 캄파니 엔브이/에스에이
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10760474&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR970705557(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 무어 제임스 더블유, 화이자 리서치 앤드 디벨롭먼트 캄파니 엔브이/에스에이 filed Critical 무어 제임스 더블유
Publication of KR970705557A publication Critical patent/KR970705557A/ko
Application granted granted Critical
Publication of KR100228952B1 publication Critical patent/KR100228952B1/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
    • C07D403/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00General protective or antinoxious agents
    • A61P39/02Antidotes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Addiction (AREA)
  • Toxicology (AREA)
  • Cardiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Nutrition Science (AREA)
  • Anesthesiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)
  • Reciprocating, Oscillating Or Vibrating Motors (AREA)

Abstract

본 발명은 하기 화학식 (Ⅰ)로 표현되는 신규한 벤즈이미다졸 유도체 또는 그의 염이다(식중, R1은 수소원자 또는 할로겐 원자이고; R2는 페닐-저급 알킬기이며; R3는 인돌일기, 인돌리닐기, 1H-인다졸일기, 2(1H)-퀴놀리노닐기, 3,4-디히드로-2(1H)-퀴놀리노닐기 및 1,4-벤즈옥사지닐기로 이루어진 군으로부터 선택된 헤테로시클릭기이고; A는 저급 알킬렌기이며, n은 0 또는 1이다). 본 발명의 신규한 벤즈이미다졸 유도체 또는 염은 다양한 동맥경화성 질병 치료에 유용한 약제이다.

Description

편두통 치료제인 인돌 유도체의 염(SALTS OF AN ANTI-MIGRAINE INDOLE DERIVATIVE)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (22)

  1. 하기 화학식(Ⅰ)의 화합물:
  2. 제1항에 있어서, 뉴졸(nujol)중의 뮬(mull)로서의 적외선 스펙트럼이 v=3371,3293,2713,2524,1419,1343,1307,1264,1151,1086,1020,1008,999,922,900,805,758,740,728,689,672,652,640,598,581,573,531,498,465,457,443,428,422,414 및 399㎝-1에서 유의한 흡수 밴드를 나타냄을 특징으로 하는 결정성, α-다형 형태의 화합물.
  3. 제2항에 있어서, 흑연 단색발광기(λ=0.15405nm)에 의해 여과된 구리 방사선을 이용하여 수득된 분말 X-선 회절패턴이 9.7, 10.7, 15.9, 16.5, 17.8, 18.9, 19.3, 19.8, 20.1, 21.2, 24.4, 25.5, 25.8, 26.7, 27.6 및 29.4°2ø에서 주 피크를 나타냄을 더욱 특징으로 하는 화합물.
  4. 제1항에 있어서, 뉴졸중의 뮬로서의 적외선 스팩트럼이 v=3239, 2672, 2656, 2632,1409,1366,1351,1334,1303,1293,1152,1138,1122,1098,1086,791,771,746,688,634,557,528,484,476,469,463,455,432,424,413 및 401㎝-1에서 유의한 흡수밴드를 나타냄을 특징으로 하는 결정성, β-다형 형태의 화합물.
  5. 제4항에 있어서, 흑연 단색발광기(λ=0.15405nm)에 의해 여과된 구리 방사선을 이용하여 수득된 분말 X-선 회절 패턴이 11.0,17.2,19.2,20.1,21.6,22.6,23.6 및 24.8°2ø에서 주 피크를 나타냄을 더욱 특징으로 하는 화합물.
  6. 약학활성이 있는 희석제 또는 담체와 함께 제1항 내지 제5항중의 어느 한 항에 따른 화합물을 포함하는 약학 조성물.
  7. 제6항에 있어서, 화학식(Ⅰ)의 화합물의 α-다형 형태를 함유하는 약학 조성물.
  8. 제6항 또는 제7항에 있어서,고형 투여 형태인 약학 조성물.
  9. 제1항 내지 제5항중의 어느 한 항에 있어서,또는 제6항 내지 제8항중의 어느 한 항에 따른 약학 조성물의 약제로서의 용도.
  10. 제9항에 있어서,화학식(Ⅰ)의 화합물의 α-다형 형태를 함유하는 화합물 또는 약학 조성물의 용도.
  11. 5-HT1수용체의 선택적인 작용물질이 처방되는 질병의 치료 또는 예방을 위한 약제의 제조용으로서의, 제1항 내지 제5항중 어느 한 항에 따른 화합물, 또는 제6항 내지 제8항중 어느 한 항에 따른 약학 조성물의 용도.
  12. 제11항에 있어서, 질병이 편두통 또는 군발성 두통, 만성 발작성 편두통 또는 혈관 이상과 연관된 두통과 관련된 질병 또는 우울증, 초조,식이 질환, 비만, 약물 남용, 고혈압 또는 구토인 용도.
  13. 제11항 또는 제12항에 있어서, 화합물이 화학식(Ⅰ)의 화합물의 α-다형 형태이거나, 또는 약학 조성물이 이를 함유하는 용도.
  14. 제1항 내지 제5항중 어느 한 항에 따른 화합물 또는 제6항 내지 제8항중 어느 한 항에 따른 약학 조성물의 효과량을 인간에게 투여함을 포함하는, 5-HT1수용체의 선택적인 작용물질이 처방되는 질병을 치료 또는 예방하기 위한 인간의 치료방법.
  15. 제14항에 있어서, 질병이 편두통, 또는 군발성 두통, 만성 발작성 편두통 또는 혈관 이상과 연관된 두통과 같은 관련된 질병 또는 우울증, 초조, 식이 질환, 비만, 약물 남용, 고혈압 또는 구토인 경우.
  16. 제14항 또는 제15항에 있어서, 화합물이 화학식(Ⅰ)의 화합물의 α-다형 형태이거나 또는 약학 조성물이 이를 함유하는 용도.
  17. a) 제1의 적합한 용매중의 하기 화학식(Ⅱ)화합물의 용액을 먼저 브롬화 수소의 수용액으로 처리시킨후, 단리되는 원유를 제2의 적합한 용매에서 결정화시킴; b) 적합한 용매에서 뉴졸중의 뮬로서의 적외선 스펙트럼이 v=3239, 2672, 2656, 2632,1409,1366,1351,1334,1303,1293,1152,1138,1122,1098,1086,791,771,746,688,634,557,528,484,476,469,463,455,432,424,413 및 401㎝-1에서 유의한 흡수밴드를 나타냄을 특징으로 하는 하기 화학식(Ⅰ)의 화합물의 β-다형 형태를 결정화시킨 후, 생성되는 혼합물을 슬러리화시킴; 또는 c) 적합한 용매중의 화학식(Ⅱ)의 화합물의 용액을 브롬화 수소의 수용액으로 처리한 후, 반응 혼합물을 슬러리화시키고, 선택적으로 환류 가열시킨후, 냉각 및 추가로 슬러리화시킴을 포함하는 뉴졸중의 뮬로서의 적외선 스펙트럼이 v=3371, 3293, 2713, 2524, 1419, 1343,1307,1264,1151,1086,1020,1008,999,922,900,805,758,740,728,689,672,640,598,581,573,531,498,465,457,443,428,422,414 및 399㎝-1에서 유의한 흡수 밴드를 나타냄을 특징으로 하는 화학식(Ⅰ)의 화합물의 결정성, α-다형 형태의 제조 방법;
  18. 제17항에 있어서, a)제1의 적합한 용매가 아세톤이고, 제2의 적합한 용매가 2-프로판올이고, 브롬화 수소의 수용액이 49% w/w이고, 20내지 25℃에서 처리되고, b)적합한 용매가 수성 아세톤이고, c)적합한 용매가 아세톤이고, 브롬화 수소의 수용액이 62% w/w이고, 0내지 5℃에서 처리되는 방법.
  19. 제17항 또는 제18항에 있어서, 화학식(Ⅰ)의 화합물의 α-다형 형태가 흑연 단색발광기(λ=0.15405nm)에 의해 여과된 구리 방사선을 이용하여 수득된 분말 X-선 회절 패턴이 9.7, 10.7, 15.9, 16.5, 17.8, 18.3, 19.3, 19.8, 20.1, 21.2, 24.4, 25.5, 25.8, 26.7, 27.6 및 29.4°2ø에서 주 피크를 나타내고, 화학식(Ⅰ)의 화합물의 β-다형이 흑연 단색발광기(λ=0.15405nm)에 의해 여과된 구리 방사선을 이용하여 수득된 분말 X-선 회절 패턴이 11.0, 17.2, 19.2, 20.1, 21.6, 22.6, 23.6 및 24.8°2ø에서 주 피크를 나타냄을 추가로 특징으로 하는 방법.
  20. 제17항 또는 제19항에 있어서, 적합한 용매중의 화학식(Ⅱ)화합물의 용액을 브롬화 수소의 수용액으로 처리함을 포함하는 화학식(Ⅰ)의 화합물의 결정성, β-다형 형태의 제조 방법.
  21. 제20항에 있어서, 적합한 용매가 아세톤, 또는 테트라하이드로푸란 또는 1,2-디메톡시에탄과 같은 에테르 용매이고, 브롬화 수소의 수용액이 49%w/w이고, 0내지 10℃에서 처리되는 방법.
  22. 제20항 또는 제21항에 있어서, 적합한 용매가 1,2-디메톡시에탄인 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019970701281A 1994-08-27 1995-05-17 편두통 치료제인 인돌 유도체의 염 KR100228952B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9417310.1 1994-08-27
GB9417310A GB9417310D0 (en) 1994-08-27 1994-08-27 Therapeutic agents
PCT/EP1995/001914 WO1996006842A1 (en) 1994-08-27 1995-05-17 Salts of an anti-migraine indole derivative

Publications (2)

Publication Number Publication Date
KR970705557A true KR970705557A (ko) 1997-10-09
KR100228952B1 KR100228952B1 (ko) 1999-11-01

Family

ID=10760474

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019970701281A KR100228952B1 (ko) 1994-08-27 1995-05-17 편두통 치료제인 인돌 유도체의 염

Country Status (45)

Country Link
US (2) US6110940A (ko)
EP (1) EP0776323B1 (ko)
JP (1) JP2904588B2 (ko)
KR (1) KR100228952B1 (ko)
CN (1) CN1066727C (ko)
AP (1) AP576A (ko)
AT (1) ATE163182T1 (ko)
AU (1) AU691005B2 (ko)
BG (1) BG61840B1 (ko)
BR (1) BRPI9503812B1 (ko)
CA (1) CA2198599C (ko)
CO (1) CO4410334A1 (ko)
CZ (1) CZ287693B6 (ko)
DE (1) DE69501620T2 (ko)
DK (1) DK0776323T3 (ko)
DZ (1) DZ1923A1 (ko)
EG (1) EG23822A (ko)
ES (1) ES2112650T3 (ko)
FI (1) FI113768B (ko)
GB (1) GB9417310D0 (ko)
GR (1) GR3026475T3 (ko)
HR (1) HRP950460B1 (ko)
HU (1) HU227822B1 (ko)
IL (1) IL115013A (ko)
IS (1) IS1850B (ko)
LV (1) LV11800B (ko)
MA (1) MA23650A1 (ko)
MX (1) MX9701538A (ko)
MY (1) MY113733A (ko)
NO (1) NO311297B1 (ko)
NZ (1) NZ288210A (ko)
OA (1) OA10600A (ko)
PE (1) PE41596A1 (ko)
PL (1) PL180867B1 (ko)
RO (1) RO116400B1 (ko)
RU (1) RU2159241C2 (ko)
SA (1) SA95160156B1 (ko)
SI (1) SI9520091B (ko)
SK (1) SK282922B6 (ko)
TN (1) TNSN95092A1 (ko)
TR (1) TR199501061A2 (ko)
UA (1) UA45980C2 (ko)
WO (1) WO1996006842A1 (ko)
YU (1) YU49287B (ko)
ZA (1) ZA957142B (ko)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9420529D0 (en) 1994-10-12 1994-11-30 Pfizer Ltd Indoles
GB9706089D0 (en) * 1997-03-24 1997-05-14 Scherer Ltd R P Pharmaceutical composition
DK0999841T3 (da) * 1997-07-03 2001-11-19 Pfizer Farmaceutiske præparater indeholdende eletriptanhemisulfat og koffein
GB9714081D0 (en) * 1997-07-03 1997-09-10 Pfizer Ltd Pharmaceutical compositions
GB9816556D0 (en) * 1998-07-30 1998-09-30 Pfizer Ltd Therapy
GB9825988D0 (en) 1998-11-27 1999-01-20 Pfizer Ltd Indole derivatives
GB9922963D0 (en) * 1999-09-28 1999-12-01 Pfizer Ltd Polymorphic salt
GB9915231D0 (en) 1999-06-29 1999-09-01 Pfizer Ltd Pharmaceutical complex
GB9923314D0 (en) 1999-10-01 1999-12-08 Pfizer Ltd Acylation process
CA2324116A1 (en) * 1999-10-25 2001-04-25 Susan Beth Sobolov-Jaynes Nk-1 receptor antagonists and eletriptan for the treatment of migraine
US6977723B2 (en) 2000-01-07 2005-12-20 Transform Pharmaceuticals, Inc. Apparatus and method for high-throughput preparation and spectroscopic classification and characterization of compositions
US7108970B2 (en) 2000-01-07 2006-09-19 Transform Pharmaceuticals, Inc. Rapid identification of conditions, compounds, or compositions that inhibit, prevent, induce, modify, or reverse transitions of physical state
GB0008563D0 (en) 2000-04-07 2000-05-24 Cambridge Discovery Chemistry Investigating different physical and/or chemical forms of materials
GB0018968D0 (en) * 2000-08-02 2000-09-20 Pfizer Ltd Particulate composition
US20030166704A1 (en) * 2000-12-20 2003-09-04 Pfizer Inc. New process
US6579898B2 (en) 2001-03-01 2003-06-17 Pfizer Inc. Compositions having improved bioavailability
EP1615635A1 (en) 2003-04-11 2006-01-18 Pfizer Limited Pharmaceutical combination comprising eletriptan and sodium bicarbonate
US7132549B2 (en) 2003-05-30 2006-11-07 Pfizer Inc. Process
GB0312478D0 (en) * 2003-05-30 2003-07-09 Pfizer Ltd Improved process
GB0317229D0 (en) * 2003-07-23 2003-08-27 Pfizer Ltd Improved process
US6927296B2 (en) 2003-07-23 2005-08-09 Pfizer Inc. Process
RU2408368C2 (ru) * 2005-06-27 2011-01-10 Биовэйл Лэборэториз Интернэшнл С.Р.Л. Препараты соли бупропиона с модифицированным высвобождением
CA2666149A1 (en) * 2006-10-19 2008-04-24 Auspex Pharmaceuticals, Inc. Substituted indoles
US20080139510A1 (en) * 2006-12-07 2008-06-12 Abe Rose Treatment of migraine headaches with sublingual amino acids
EP1956018A1 (de) * 2007-02-06 2008-08-13 Boehringer Ingelheim Pharma GmbH & Co. KG Verfahren zur Herstellung eines Benzimidazolderivats
WO2008137134A2 (en) * 2007-05-01 2008-11-13 Teva Pharmaceuticals Usa, Inc. Amorphous eletriptan hydrobromide and process for preparing it and other forms of eletriptan hydrobromide
US20080319205A1 (en) * 2007-05-29 2008-12-25 Roman Bednar Process for preparing 5-bromo-3-[(R)-1-methyl-pyrrolidin-2-ylmethyl]-1H-indole
WO2009077858A2 (en) * 2007-12-17 2009-06-25 Actavis Group Ptc Ehf Novel hemioxalate salt of eletriptan
US20090299077A1 (en) * 2008-05-22 2009-12-03 Vinod Kumar Kansal Salts of (R)-5-(2phenylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole, 5-bromo-3-[(R)-1-methyl-pyrrolidin-2-ylmethyl]-1H-indole and of eletriptan
WO2010015692A2 (en) * 2008-08-07 2010-02-11 Biovail Laboratories International Srl Bupropion hydrobromide polymorphs
US20120027816A1 (en) * 2009-02-25 2012-02-02 Actavis Group Ptc Ehf Highly pure eletriptan or a pharmaceutically acceptable salt thereof substantially free of eletriptan n-oxide impurity
WO2010116386A2 (en) * 2009-04-08 2010-10-14 Biophore India Pharmaceuticals Pvt. Ltd. Novel polymorph of eletriptan hydrobromide and process for the preparation thereof
IT1393700B1 (it) 2009-04-22 2012-05-08 F S I Fabbrica Italiana Sint Sintesi di 3-{[(2r)-1-metilpirrolidin-2-il]metil}-5-[2-(fenilsulfonil)etil]-1h-indolo
WO2011004391A2 (en) 2009-06-25 2011-01-13 Matrix Laboratories Ltd An improved process for the preparation of eletriptan and its salt thereof
WO2011089614A1 (en) * 2010-01-19 2011-07-28 Sms Pharmaceuticals Limited PROCESS FOR PREPARING ELETRIPTAN HYDROBROMIDE HAVING α-FORM
WO2014063752A1 (en) 2012-10-26 2014-05-01 Synthon Bv Process for making crystalline form alpha of eletriptan hydrobromide
JP2019502761A (ja) 2016-01-21 2019-01-31 ラボラトリオス レヴィ エセエレ ((r)−3−[(−1−メチルピロリジン−2−イル)メチル]−5−(2−フェニルスルホニルエチル)−1h−インドールを作製する方法

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2773875A (en) * 1952-03-28 1956-12-11 Hoffmann La Roche Indole derivatives and method for producing same
GB886684A (en) * 1957-09-17 1962-01-10 Upjohn Co Improvements in or relating to heterocyclic compounds and the manufacture thereof
GB851780A (en) * 1958-02-25 1960-10-19 Rhone Poulenc Sa New indole derivatives
US3037031A (en) * 1959-08-04 1962-05-29 Warner Lambert Pharmaceutical Derivatives of 3-(2-aminoalkyl)-5-indolol and process therefor
GB893707A (en) * 1960-03-01 1962-04-11 Roche Products Ltd Novel tryptamine derivatives and a process for the manufacture thereof
GB966562A (en) * 1961-04-06 1964-08-12 Parke Davis & Co Amine compounds and means of producing the same
US4092315A (en) * 1976-03-01 1978-05-30 Pfizer Inc. Novel crystalline forms of prazosin hydrochloride
ZA795239B (en) * 1978-10-12 1980-11-26 Glaxo Group Ltd Heterocyclic compounds
ZW19381A1 (en) * 1980-08-12 1983-03-09 Glaxo Group Ltd Heterocyclic compounds
US4803218A (en) * 1982-09-29 1989-02-07 Mcneilab, Inc. 3-aminoalkyl-1H-indole-5-urea and amide derivatives
GB8600397D0 (en) * 1986-01-08 1986-02-12 Glaxo Group Ltd Chemical compounds
DK158590D0 (da) * 1990-07-02 1990-07-02 Lundbeck & Co As H Indolderivater
US5578612A (en) * 1990-10-15 1996-11-26 Pfizer Inc. Indole derivatives
US5545644A (en) * 1990-10-15 1996-08-13 Pfizer Inc. Indole derivatives
KR0179053B1 (ko) * 1990-10-15 1999-03-20 알렌 제이.스피겔 인돌 유도체
US5559246A (en) * 1990-10-15 1996-09-24 Pfizer Inc. Indole derivatives
US5559129A (en) * 1990-10-15 1996-09-24 Pfizer Inc Indole derivatives
US5208248A (en) * 1991-01-11 1993-05-04 Merck Sharpe & Dohme, Ltd. Indazole-substituted five-membered heteroaromatic compounds
CZ283018B6 (cs) * 1991-02-01 1997-12-17 Merck Sharp And Dohme Limited Deriváty imidazolu, triazolu a tetrazolu a farmaceutické přípravky na jejich bázi
ES2143992T3 (es) * 1991-11-25 2000-06-01 Pfizer Derivados de 5-(hetero- o carbociclilamino)-indol, su preparacion y uso como 5-ht1 agonistas.
GB9201038D0 (en) * 1992-01-16 1992-03-11 Glaxo Group Ltd Chemical compounds
US5409941A (en) * 1992-02-03 1995-04-25 Pfizer Inc. 5-heteroyl indole derivatives
TW288010B (ko) * 1992-03-05 1996-10-11 Pfizer
KR0179072B1 (ko) * 1992-04-07 1999-03-20 알렌 제이. 스피겔 5-ht1 작동약으로서의 인돌 유도체
KR0179074B1 (ko) * 1992-04-10 1999-03-20 알렌 제이. 스피겔 5-ht1 작용물질로서의 아실아미노인돌 유도체
GB9207930D0 (en) * 1992-04-10 1992-05-27 Pfizer Ltd Indoles
GB9208161D0 (en) * 1992-04-14 1992-05-27 Pfizer Ltd Indoles
GB9210400D0 (en) * 1992-05-15 1992-07-01 Merck Sharp & Dohme Therapeutic agents
FR2701026B1 (fr) * 1993-02-02 1995-03-31 Adir Nouveaux dérivés de l'indole, de l'indazole et du benzisoxazole, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
CN1121348A (zh) * 1993-04-22 1996-04-24 辉瑞研究及发展公司 吲哚衍生物作为5-ht1类激动剂用于治疗周期性偏头痛
AP486A (en) * 1993-04-27 1996-04-16 Pfizer Indole derivatives.
ATE170836T1 (de) * 1993-08-31 1998-09-15 Pfizer 5-arylindolderivate

Also Published As

Publication number Publication date
EP0776323B1 (en) 1998-02-11
FI970800A0 (fi) 1997-02-26
YU49287B (sh) 2005-03-15
BRPI9503812B1 (pt) 2017-04-18
CN1066727C (zh) 2001-06-06
EG23822A (en) 2007-09-19
CZ56397A3 (cs) 1998-05-13
YU56995A (sh) 1998-07-10
MX9701538A (es) 1997-05-31
FI970800A (fi) 1997-02-26
DE69501620D1 (de) 1998-03-19
US6380226B1 (en) 2002-04-30
NO970861L (no) 1997-02-26
NZ288210A (en) 1998-01-26
RO116400B1 (ro) 2001-01-30
CN1155886A (zh) 1997-07-30
ES2112650T3 (es) 1998-04-01
ZA957142B (en) 1997-02-25
MA23650A1 (fr) 1996-04-01
AP576A (en) 1997-03-20
CA2198599A1 (en) 1996-03-07
PL180867B1 (pl) 2001-04-30
NO970861D0 (no) 1997-02-26
AU691005B2 (en) 1998-05-07
JPH09512283A (ja) 1997-12-09
KR100228952B1 (ko) 1999-11-01
LV11800A (lv) 1997-06-20
PE41596A1 (es) 1996-10-12
UA45980C2 (uk) 2002-05-15
SI9520091A (sl) 1998-02-28
HRP950460B1 (en) 2000-02-29
AU2735295A (en) 1996-03-22
PL318319A1 (en) 1997-06-09
ATE163182T1 (de) 1998-02-15
IL115013A0 (en) 1995-12-08
DZ1923A1 (fr) 2002-02-17
GB9417310D0 (en) 1994-10-19
IS4401A (is) 1996-12-19
GR3026475T3 (en) 1998-06-30
BG61840B1 (bg) 1998-07-31
HU227822B1 (en) 2012-03-28
JP2904588B2 (ja) 1999-06-14
SA95160156B1 (ar) 2005-05-30
EP0776323A1 (en) 1997-06-04
WO1996006842A1 (en) 1996-03-07
CO4410334A1 (es) 1997-01-09
BG101250A (en) 1997-09-30
AP9500754A0 (en) 1995-07-31
SI9520091B (sl) 2004-10-31
DK0776323T3 (da) 1998-03-30
IL115013A (en) 2000-11-21
FI113768B (fi) 2004-06-15
TNSN95092A1 (fr) 1996-02-06
LV11800B (en) 1997-10-20
OA10600A (en) 2000-04-06
RU2159241C2 (ru) 2000-11-20
IS1850B (is) 2003-02-07
US6110940A (en) 2000-08-29
HRP950460A2 (en) 1997-08-31
CZ287693B6 (en) 2001-01-17
SK24897A3 (en) 1998-08-05
CA2198599C (en) 2000-06-06
DE69501620T2 (de) 1998-07-02
TR199501061A2 (tr) 1996-06-21
BR9503812A (pt) 1996-04-16
NO311297B1 (no) 2001-11-12
HUT77310A (hu) 1998-03-30
SK282922B6 (sk) 2003-01-09
MY113733A (en) 2002-05-31

Similar Documents

Publication Publication Date Title
KR970705557A (ko) 편두통 치료제인 인돌 유도체의 염(salts of an anti-migraine indole derivative)
RU97104885A (ru) Соли производного индола против мигрени
LV12792A (en) Formyl- or cyano- indole derivatives having dopaminergic activity
JPH0369898B2 (ko)
RU94045897A (ru) Производные индола в качестве 5-hti-агонистов, фармацевтическая композиция и способ лечения
WO1997037989A1 (en) Indole derivatives as 5-ht receptor antagonist
AP535A (en) Indoline derivatives, method of preparation and use.
JPH08512299A (ja) 5ht▲下2c▼アンタゴニストとしてのインドリン誘導体
JP2517725B2 (ja) 1H,3H−ピロロ〔1,2−c〕チアゾ−ル誘導体、その製造法および薬としての用途
DE69617995T2 (de) Indolalkylderivate von benzodioxanmenthylamin als 5-ht1a rezeptor liganden
FR2548666A1 (fr) Nouveaux derives du nor-tropane et du granatane, leur procede de preparation et leur application en therapeutique
JP2865255B2 (ja) 1,2,3,4,10,14b‐ヘキサヒドロジベンゾ〔c,f〕ピラジノ〔1,2‐a〕アゼピノ誘導体及び10‐アザ,10‐オキサ及び10‐チア類似体
AP2004A (en) Polymorphic salt as an anti-migraine drug.
EP0646110B1 (de) N-substituierte 3-azabicyclo[3.2.0]heptan-derivate als neuroleptika
US4217356A (en) 2-Imidazolinylamino-2,1,3-benzothiadiazoles
CZ46896A3 (en) Anti-migraine 1,2,5-thiadiazole derivatives of indolylalkyl-pyridinyl and -pyrimidinyl piperazines
Cannon et al. 6-Hydroxy-4-[2-di-n-propylaminoethyl] indole: synthesis and dopaminergic actions
DE3779916T2 (de) Anthelmintische acylhydrazone, verfahren zur verwendung und zusammensetzungen.
EP0463944B1 (fr) Acyl benzoxazolinones, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent
EP0105821B1 (fr) Nouvelles N-(aminométhyl-5-oxazolin-2-yl-2)N'-phénylurées
EP0304353A1 (fr) Dérivés de benzimidazole et leur préparation
NL8301269A (nl) Werkwijze ter bereiding van nieuwe furanderivaten.
JP2023539043A (ja) ベンジルアミン誘導体、その調製方法およびその用途
FR2552083A1 (fr) Derives de (alkynyloxy-3 hydroxy-2-propyl)-4 piperazinyl-1 n-phenyl acetamide, leur preparation et leur application en therapeutique
JPH0222252A (ja) 5―ヒドロキシトリプタミン―1a―受容体結合化合物

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120727

Year of fee payment: 14

FPAY Annual fee payment

Payment date: 20130729

Year of fee payment: 15

FPAY Annual fee payment

Payment date: 20140730

Year of fee payment: 16

EXPY Expiration of term