KR860003240A - 1,2,4- 트리아졸로- 카바메이트의 제조방법 - Google Patents
1,2,4- 트리아졸로- 카바메이트의 제조방법 Download PDFInfo
- Publication number
- KR860003240A KR860003240A KR1019850007921A KR850007921A KR860003240A KR 860003240 A KR860003240 A KR 860003240A KR 1019850007921 A KR1019850007921 A KR 1019850007921A KR 850007921 A KR850007921 A KR 850007921A KR 860003240 A KR860003240 A KR 860003240A
- Authority
- KR
- South Korea
- Prior art keywords
- methyl
- formula
- prepared
- carbon atoms
- triazole
- Prior art date
- 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.)
- Withdrawn
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- -1 chlor-substituted phenyl Chemical group 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- KSDHWHYTKGBNLD-UHFFFAOYSA-N [4-(4-chlorophenyl)-5-ethyl-1,2,4-triazol-3-yl] 4-methylpiperazine-1-carboxylate Chemical compound C=1C=C(Cl)C=CC=1N1C(CC)=NN=C1OC(=O)N1CCN(C)CC1 KSDHWHYTKGBNLD-UHFFFAOYSA-N 0.000 claims 1
- WSVLQCSQYCFRIF-UHFFFAOYSA-N [4-(4-chlorophenyl)-5-methyl-1,2,4-triazol-3-yl] 4-methylpiperazine-1-carboxylate Chemical compound C1CN(C)CCN1C(=O)OC1=NN=C(C)N1C1=CC=C(Cl)C=C1 WSVLQCSQYCFRIF-UHFFFAOYSA-N 0.000 claims 1
- NZBXIPRHVGXOOC-UHFFFAOYSA-N [4-(5-chloropyridin-2-yl)-5-methyl-1,2,4-triazol-3-yl] 4-methylpiperazine-1-carboxylate Chemical compound C1CN(C)CCN1C(=O)OC1=NN=C(C)N1C1=CC=C(Cl)C=N1 NZBXIPRHVGXOOC-UHFFFAOYSA-N 0.000 claims 1
- KWOQJDDWPPGMTD-UHFFFAOYSA-N [4-(5-chloropyridin-2-yl)-5-methyl-1,2,4-triazol-3-yl] n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC1=NN=C(C)N1C1=CC=C(Cl)C=N1 KWOQJDDWPPGMTD-UHFFFAOYSA-N 0.000 claims 1
- DUOUEDBIQDCCQM-UHFFFAOYSA-N [4-(5-chloropyridin-2-yl)-5-methyl-1,2,4-triazol-3-yl] n-methylcarbamate Chemical compound CNC(=O)OC1=NN=C(C)N1C1=CC=C(Cl)C=N1 DUOUEDBIQDCCQM-UHFFFAOYSA-N 0.000 claims 1
- WQNKWQYVJJJMQT-UHFFFAOYSA-N [4-(5-chloropyridin-2-yl)-5-methyl-1,2,4-triazol-3-yl] n-tert-butylcarbamate Chemical compound CC1=NN=C(OC(=O)NC(C)(C)C)N1C1=CC=C(Cl)C=N1 WQNKWQYVJJJMQT-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 231100000252 nontoxic Toxicity 0.000 claims 1
- 230000003000 nontoxic effect Effects 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- C07D213/02—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
- 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
- C07D213/60—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 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Neurology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 일반식(Ⅱ)의 화합물을, 임의로는 염기를 첨가하여, 일반식(Ⅲ)의 할로카보닐아미드와 반응시키거나 일반식(Ⅳ)의 할로카보네이트와 반응시킨 다음, 이어서 일반식(Ⅴ)의 1급 또는 2급과 아민과 반응시키거나; 일반식(Ⅵ)의 카바미드산 에스테르와 반응시키거나; R3가 수소인 화합물을 제조하는 경우에는 일반식(Ⅶ)의 이소시아네이트와 반응시키고, 임의로는 염형성시킴을 특징으로 하여 일반식(Ⅰ)의 화합물 또는 생리학적으로 무독한 이의 산 부가염을 제조하는 방법.상기식에서, R1은 수소, 탄소수 1 내지 8의 직쇄 또는 측쇄 알킬, 3원 내지 6원의 카보사이클릭환, 벤질 또는 펜에틸이고; R2는 할로겐, 메틸, 메톡시 또는 트리플루오로메틸로 일-또는 이-치환될 수 있는 페닐 또는 피리디닐 그룹이며; R3및 R4는 동일하거나 상이하며, 수소, 탄소수 1 내지 6의 직쇄 또는 측쇄 알킬, 탄소수 3 내지 6의 사이클로알킬이거나, 할로겐, 메톡시, 트리플루오로메틸 또는 탄소수 1 내지 6의 직쇄 또는 측쇄 알킬로 임의 치환된 아릴 또는 헤테로아릴그룹이거나, R3및 R4가 질소원자와 함께 탄소수 1 내지 4의 직쇄 또는 측쇄 알킬그룹 하나 이상으로 임의 치환된 5원 또는 6원의 포화환일 수 있고[여기서, 5원 도는 6원환은 추가의 헤테로원자로서 질소, 산소 또는 황을 함유할 수 있으며, 질소를 함유하는 경우에는 탄소수 1 내지 4의 알킬그룹 또는 탄소수 1 내지 3의 하이드록시알킬그룹으로 치환될 수 있다]; X는 할로겐, 바람직하게는 염소이며; R5는 이탈그룹으로서 적절한 알킬 또는 아릴 그룹이다.
- 제1항에 있어서, 일반식(Ⅱ)의 화합물을 염기와 반응시켜 이의 염으로 전환시킨 다음, 일반식(Ⅲ),(Ⅳ) 또는 (Ⅵ)의 화합물과 반응시키는 방법.
- 제1항에 있어서, R1이 메틸 또는 에틸그룹이고; R2는 염소-치환된 페닐 또는 피리디닐그룹이며; R3는 수소, 또는 메틸 또는 에틸 그룹이고; R4는 탄소수 1 내지 4의 저급 알킬그룹이거나, 또는 R3와 R4가 질소원자와 함께 N-메틸치환된 피페라지닐그룹을 형성하는 일반식(Ⅰ)의 화합물을 제조하는 방법.
- 제1항에 있어서, 4-(5-클로로피리딘-2-일)-3-메틸-5-[(4-메틸피페라지닐)카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(5-클로로피리딘-2-일)-3-메틸-5-[N-3급-부틸아미노카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(4-클로로페닐)-3-에틸-5-[(4-메틸피페라지닐)카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(5-클로로피리딘-2-일)-3-메틸-5-[N-디에틸아미노카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(5-클로로피리딘-2-일)-3-메틸-5-[N-메틸아미노카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(5-클로로피리딘-2-일)-3-메틸-5-[N,N-디메틸아미노카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.
- 제1항에 있어서, 4-(4-클로로페닐)-3-메틸-5-[(4-메틸피페라지닐)카보닐]옥시-1,2,4-트리아졸을 제조하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19843439450 DE3439450A1 (de) | 1984-10-27 | 1984-10-27 | 1,2,4-triazolo-carbamate und ihre saeureadditionssalze, verfahren zu ihrer herstellung und arzneimittel |
DEP3439450.8 | 1984-10-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR860003240A true KR860003240A (ko) | 1986-05-21 |
Family
ID=6248953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850007921A Withdrawn KR860003240A (ko) | 1984-10-27 | 1985-10-26 | 1,2,4- 트리아졸로- 카바메이트의 제조방법 |
Country Status (22)
Country | Link |
---|---|
US (1) | US4732900A (ko) |
EP (1) | EP0180115A3 (ko) |
JP (1) | JPS61103876A (ko) |
KR (1) | KR860003240A (ko) |
AU (1) | AU576393B2 (ko) |
CA (1) | CA1244030A (ko) |
CS (2) | CS255897B2 (ko) |
DD (1) | DD236928A5 (ko) |
DE (1) | DE3439450A1 (ko) |
DK (1) | DK491385A (ko) |
ES (2) | ES8701738A1 (ko) |
FI (1) | FI854178A7 (ko) |
GR (1) | GR852581B (ko) |
HU (1) | HU193351B (ko) |
IL (1) | IL76823A0 (ko) |
NO (1) | NO854276L (ko) |
NZ (1) | NZ213969A (ko) |
PH (1) | PH22446A (ko) |
PL (2) | PL264492A1 (ko) |
PT (1) | PT81370B (ko) |
SU (2) | SU1436873A3 (ko) |
ZA (1) | ZA858195B (ko) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2784921B2 (ja) * | 1988-03-23 | 1998-08-13 | 武田薬品工業株式会社 | カルバメート化合物 |
US5331002A (en) * | 1990-04-19 | 1994-07-19 | Merrell Dow Pharmaceuticals Inc. | 5-aryl-4-alkyl-3H-1,2,4-triazole-3-thiones useful as memory enhancers |
US5100906A (en) * | 1990-04-19 | 1992-03-31 | Merrell Dow Pharmaceuticals Inc. | 5-aryl-4-alkyl-3h-1,2,4-triazole-3-thiones useful as memory enhancers |
DE4234801A1 (de) * | 1992-10-15 | 1994-04-21 | Bayer Ag | Sulfonylaminocarbonyltriazolinone |
DE4425144A1 (de) * | 1994-07-15 | 1996-01-18 | Basf Ag | Triazolverbindungen und deren Verwendung |
US5728834A (en) * | 1996-11-14 | 1998-03-17 | Wyckoff Chemical Company, Inc. | Process for preparation of 4-aryl-1,2,4-triazol-3-ones |
MXPA06011046A (es) * | 2004-03-26 | 2007-03-21 | Amphora Discovery Corp | Ciertos compuestos basados en triazol, composiciones, y usos de los mismos. |
US8084451B2 (en) * | 2005-01-10 | 2011-12-27 | University Of Connecticut | Heteropyrrole analogs acting on cannabinoid receptors |
US8853205B2 (en) | 2005-01-10 | 2014-10-07 | University Of Connecticut | Heteropyrrole analogs acting on cannabinoid receptors |
US10053444B2 (en) | 2009-02-19 | 2018-08-21 | University Of Connecticut | Cannabinergic nitrate esters and related analogs |
CA3125847A1 (en) | 2020-07-27 | 2022-01-27 | Makscientific, Llc | Process for making biologically active compounds and intermediates thereof |
US12054480B2 (en) | 2020-07-31 | 2024-08-06 | Makscientific, Llc | Compounds for treating cannabinoid toxicity and acute cannabinoid overdose |
CN115991698B (zh) * | 2022-11-03 | 2024-03-29 | 广东中科药物研究有限公司 | 一种杂环化合物及其制备方法与应用 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB681376A (en) * | 1949-11-23 | 1952-10-22 | Geigy Ag J R | Manufacture of heterocyclic carbamic acid derivatives and their use as agents for combating pests |
NL7112373A (ko) * | 1970-09-25 | 1972-03-28 | ||
US4209515A (en) * | 1974-06-14 | 1980-06-24 | Ciba-Geigy Corporation | Triazole derivatives |
US4160839A (en) * | 1976-03-01 | 1979-07-10 | Gulf Oil Corporation | Carbamyltriazole insecticides |
JPS59199681A (ja) * | 1983-04-26 | 1984-11-12 | Ube Ind Ltd | 1,2,4−トリアゾ−ル−3−カルボン酸アミド類の製造法 |
FI850994L (fi) * | 1984-03-16 | 1985-09-17 | Ciba Geigy Ag | Foerfarande foer framstaellning av nya 1,2,4-triazacykloalkadienderivat. |
US4610717A (en) * | 1985-11-26 | 1986-09-09 | Shell Oil Company | Certain 5-(R-oxy)-1-phenyl or (3-(trifluoromethyl)phenyl)triazoles, useful for controlling undesired plant growth |
-
1984
- 1984-10-27 DE DE19843439450 patent/DE3439450A1/de not_active Withdrawn
-
1985
- 1985-10-19 EP EP85113278A patent/EP0180115A3/de not_active Withdrawn
- 1985-10-22 SU SU853965776A patent/SU1436873A3/ru active
- 1985-10-23 CS CS857593A patent/CS255897B2/cs unknown
- 1985-10-23 CS CS864625A patent/CS255877B2/cs unknown
- 1985-10-24 JP JP60236563A patent/JPS61103876A/ja active Pending
- 1985-10-25 PH PH32968A patent/PH22446A/en unknown
- 1985-10-25 NZ NZ213969A patent/NZ213969A/en unknown
- 1985-10-25 US US06/791,184 patent/US4732900A/en not_active Expired - Fee Related
- 1985-10-25 FI FI854178A patent/FI854178A7/fi not_active IP Right Cessation
- 1985-10-25 PT PT81370A patent/PT81370B/pt unknown
- 1985-10-25 PL PL1985264492A patent/PL264492A1/xx unknown
- 1985-10-25 AU AU49094/85A patent/AU576393B2/en not_active Withdrawn - After Issue
- 1985-10-25 HU HU854123A patent/HU193351B/hu unknown
- 1985-10-25 DK DK491385A patent/DK491385A/da not_active Application Discontinuation
- 1985-10-25 NO NO854276A patent/NO854276L/no unknown
- 1985-10-25 GR GR852581A patent/GR852581B/el unknown
- 1985-10-25 ZA ZA858195A patent/ZA858195B/xx unknown
- 1985-10-25 CA CA000493928A patent/CA1244030A/en not_active Expired
- 1985-10-25 IL IL76823A patent/IL76823A0/xx unknown
- 1985-10-25 DD DD85282074A patent/DD236928A5/de unknown
- 1985-10-25 ES ES548206A patent/ES8701738A1/es not_active Expired
- 1985-10-25 PL PL25594085A patent/PL255940A1/xx unknown
- 1985-10-26 KR KR1019850007921A patent/KR860003240A/ko not_active Withdrawn
-
1986
- 1986-04-25 ES ES554373A patent/ES8704468A1/es not_active Expired
- 1986-11-11 SU SU864028478A patent/SU1429934A3/ru active
Also Published As
Publication number | Publication date |
---|---|
HU193351B (en) | 1987-09-28 |
ES548206A0 (es) | 1986-12-01 |
PH22446A (en) | 1988-09-12 |
DE3439450A1 (de) | 1986-05-07 |
ES8704468A1 (es) | 1987-04-01 |
FI854178A0 (fi) | 1985-10-25 |
NZ213969A (en) | 1987-11-27 |
DD236928A5 (de) | 1986-06-25 |
AU4909485A (en) | 1986-05-01 |
US4732900A (en) | 1988-03-22 |
IL76823A0 (en) | 1986-02-28 |
EP0180115A3 (de) | 1987-01-21 |
CA1244030A (en) | 1988-11-01 |
CS255877B2 (en) | 1988-03-15 |
JPS61103876A (ja) | 1986-05-22 |
PL255940A1 (en) | 1987-07-13 |
ES8701738A1 (es) | 1986-12-01 |
ES554373A0 (es) | 1987-04-01 |
EP0180115A2 (de) | 1986-05-07 |
NO854276L (no) | 1986-04-28 |
GR852581B (ko) | 1986-02-26 |
FI854178L (fi) | 1986-04-28 |
PT81370B (de) | 1987-08-20 |
HUT40091A (en) | 1986-11-28 |
DK491385D0 (da) | 1985-10-25 |
SU1436873A3 (ru) | 1988-11-07 |
SU1429934A3 (ru) | 1988-10-07 |
DK491385A (da) | 1986-04-28 |
CS255897B2 (en) | 1988-03-15 |
AU576393B2 (en) | 1988-08-25 |
FI854178A7 (fi) | 1986-04-28 |
PT81370A (de) | 1985-11-01 |
PL264492A1 (en) | 1987-11-30 |
ZA858195B (en) | 1987-06-24 |
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Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19851026 |
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PC1203 | Withdrawal of no request for examination | ||
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |