DD150893A5 - Verfahren zur herstellung von reinem trans-3-(4-tert.-butyl-cyclohexyl-1')-2-methyl-1-(3'-methylpiperidino-,-3',5'-dimethylpiperidino-und-2',6'-dimethylmorph olino)-propan - Google Patents

Verfahren zur herstellung von reinem trans-3-(4-tert.-butyl-cyclohexyl-1')-2-methyl-1-(3'-methylpiperidino-,-3',5'-dimethylpiperidino-und-2',6'-dimethylmorph olino)-propan Download PDF

Info

Publication number: DD150893A5
Authority: DD; German Democratic Republic
Prior art keywords: trans; methyl; cis; tert; propane
Prior art date: 1979-05-25

Application number

DD80221320A

Other languages

German (de)

English (en)

Inventor

Walter Himmele

Wolfgang Heberle

Wilhelm Kohlmann

Walter Wesenberg

Original Assignee

Basf Ag

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.)

1979-05-25

Filing date

1980-05-22

Publication date

1981-09-23

1980-05-22 Application filed by Basf Ag filed Critical Basf Ag

1981-09-23 Publication of DD150893A5 publication Critical patent/DD150893A5/de

Links

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235000019437 butane-1,3-diol Nutrition 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
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239000002775 capsule Substances 0.000 description 1
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150000004292 cyclic ethers Chemical class 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
150000001983 dialkylethers Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000007884 disintegrant Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
230000002289 effect on microbe Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
229940093499 ethyl acetate Drugs 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
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238000009472 formulation Methods 0.000 description 1
238000001640 fractional crystallisation Methods 0.000 description 1
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235000011852 gelatine desserts Nutrition 0.000 description 1
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YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
229940074076 glycerol formal Drugs 0.000 description 1
SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000006210 lotion Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000002780 morpholines Chemical class 0.000 description 1
235000001968 nicotinic acid Nutrition 0.000 description 1
229960003512 nicotinic acid Drugs 0.000 description 1
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229910017604 nitric acid Inorganic materials 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
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230000003287 optical effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000000312 peanut oil Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000006187 pill Substances 0.000 description 1
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
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229920001296 polysiloxane Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229940075065 polyvinyl acetate Drugs 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000003380 propellant Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
229960004063 propylene glycol Drugs 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
229940081974 saccharin Drugs 0.000 description 1
235000019204 saccharin Nutrition 0.000 description 1
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000008159 sesame oil Substances 0.000 description 1
235000011803 sesame oil Nutrition 0.000 description 1
239000004208 shellac Substances 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
239000004332 silver Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000007910 systemic administration Methods 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
239000002700 tablet coating Substances 0.000 description 1
238000009492 tablet coating Methods 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
238000011200 topical administration Methods 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
230000007704 transition Effects 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical group COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
235000012141 vanillin Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
239000001993 wax Substances 0.000 description 1
235000014692 zinc oxide Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/03—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Communicable Diseases (AREA)
Animal Behavior & Ethology (AREA)
Oncology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Hydrogenated Pyridines (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD80221320A 1979-05-25 1980-05-22 Verfahren zur herstellung von reinem trans-3-(4-tert.-butyl-cyclohexyl-1')-2-methyl-1-(3'-methylpiperidino-,-3',5'-dimethylpiperidino-und-2',6'-dimethylmorph olino)-propan DD150893A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792921221 DE2921221A1 (de)	1979-05-25	1979-05-25	Trans-3-(4'-tert.-butyl-cyclohexyl-1')- 2-methyl-1-(3'-methylpiperidino, 3', 5'- dimethylpiperidino und 2', 6'-dimethylmorpholino)-propan, verfahren zu ihrer reinherstellung und diese enthaltende antimykotische mittel

Publications (1)

Publication Number	Publication Date
DD150893A5 true DD150893A5 (de)	1981-09-23

Family

ID=6071686

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80221320A DD150893A5 (de)	1979-05-25	1980-05-22	Verfahren zur herstellung von reinem trans-3-(4-tert.-butyl-cyclohexyl-1')-2-methyl-1-(3'-methylpiperidino-,-3',5'-dimethylpiperidino-und-2',6'-dimethylmorph olino)-propan

Country Status (14)

Country	Link
EP (1)	EP0019764A1 (da)
JP (1)	JPS55157567A (da)
AU (1)	AU5871080A (da)
CA (1)	CA1146551A (da)
CS (1)	CS214831B2 (da)
DD (1)	DD150893A5 (da)
DE (1)	DE2921221A1 (da)
DK (1)	DK226080A (da)
ES (1)	ES491793A0 (da)
FI (1)	FI801364A7 (da)
HU (1)	HU179864B (da)
IL (1)	IL59956A0 (da)
NO (1)	NO801556L (da)
ZA (1)	ZA803108B (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3001581A1 (de) *	1980-01-17	1981-07-23	Basf Ag, 6700 Ludwigshafen	Substituierte n- (3(4'-tert-butyl-cyclohex-1'-en1'yl)-2-methyl-propyl-1) -cycloalkalamine, ihre herstellung und ihre anwendung als fungizide
DE3225879A1 (de) *	1982-07-10	1984-01-12	Basf Ag, 6700 Ludwigshafen	Trans-3-(4'-tert.-butylcyclohexyl-1')-2-methyl-1-dialkyl-aminopropane, ihre herstellung und verwendung als arzneimittel
DE3321712A1 (de) *	1983-06-16	1984-12-20	Basf Ag, 6700 Ludwigshafen	2,6-trans-dimethylmorpholinderivate und diese enthaltende fungizide und verfahren zur bekaempfung von pilzen
JP6105587B2 (ja)	2011-08-29	2017-04-05	セラロック、イノベーション、アクチボラグ	フロアパネル用機械式係止システム

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE614214A (da) *	1961-02-22
DE1214471B (de) *	1965-01-16	1966-04-14	Basf Ag	Fungizid fuer den Pflanzenschutz
AT354187B (de) *	1976-11-22	1979-12-27	Hoffmann La Roche	Fungizides mittel
DE2657476A1 (de) *	1976-12-18	1978-06-22	Basf Ag	Morpholinderivate
DE2830127A1 (de) *	1978-07-08	1980-01-17	Basf Ag	N-arylpropyl-substituierte cyclische amine
ATE3111T1 (de) *	1978-08-08	1983-05-15	F. Hoffmann-La Roche & Co. Aktiengesellschaft	Verfahren zur herstellung von phenyl-propylmorpholin- und -piperidin-derivaten.

1979
- 1979-05-25 DE DE19792921221 patent/DE2921221A1/de not_active Withdrawn
1980
- 1980-04-28 FI FI801364A patent/FI801364A7/fi not_active Application Discontinuation
- 1980-04-30 IL IL59956A patent/IL59956A0/xx unknown
- 1980-05-05 CA CA000351285A patent/CA1146551A/en not_active Expired
- 1980-05-08 EP EP80102509A patent/EP0019764A1/de not_active Withdrawn
- 1980-05-22 JP JP6721680A patent/JPS55157567A/ja active Pending
- 1980-05-22 DD DD80221320A patent/DD150893A5/de unknown
- 1980-05-23 ES ES491793A patent/ES491793A0/es active Granted
- 1980-05-23 HU HU80801307A patent/HU179864B/hu unknown
- 1980-05-23 AU AU58710/80A patent/AU5871080A/en not_active Abandoned
- 1980-05-23 NO NO801556A patent/NO801556L/no unknown
- 1980-05-23 DK DK226080A patent/DK226080A/da unknown
- 1980-05-23 ZA ZA00803108A patent/ZA803108B/xx unknown
- 1980-05-23 CS CS803655A patent/CS214831B2/cs unknown

Also Published As

Publication number	Publication date
HU179864B (en)	1982-12-28
CA1146551A (en)	1983-05-17
CS214831B2 (en)	1982-06-25
IL59956A0 (en)	1980-06-30
JPS55157567A (en)	1980-12-08
DE2921221A1 (de)	1980-12-11
EP0019764A1 (de)	1980-12-10
ES8102095A1 (es)	1980-12-16
NO801556L (no)	1980-11-26
ZA803108B (en)	1981-06-24
FI801364A7 (fi)	1980-11-26
ES491793A0 (es)	1980-12-16
DK226080A (da)	1980-11-26
AU5871080A (en)	1980-11-27

Publication	Publication Date	Title
EP0828484A1 (de)	1998-03-18	Verwendung arylsubstituierter cyclobutylalkylamine zur behandlung der fettleibigkeit
DE4243279A1 (de)	1994-06-23	Substituierte Triole
DE2920437A1 (de)	1980-11-27	Geometrische isomere von 4,4- dimethyl-1-phenyl-2-(1,2,4-triazol-1-yl)- 1-penten-3-olen, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
DD150893A5 (de)	1981-09-23	Verfahren zur herstellung von reinem trans-3-(4-tert.-butyl-cyclohexyl-1')-2-methyl-1-(3'-methylpiperidino-,-3',5'-dimethylpiperidino-und-2',6'-dimethylmorph olino)-propan
US4487965A (en)	1984-12-11	Trans-3-(4'-tert.-Butylcyclohex-1'yl)-2-methyl-1-dialkylaminopropanes, their preparation and their use as drugs
DE1695140A1 (de)	1970-12-17	Verfahren zur Herstellung von Phenanthridinderivaten
DE2507429C2 (de)	1982-10-07	Aminosäureester, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
DE1915230A1 (de)	1970-02-05	Hydroxyphenylalkylaminderivate und Verfahren zu deren Herstellung
EP0401798B1 (de)	1995-01-11	Substituierte Aminoalkylbenzolderivate
EP0009776B1 (de)	1982-07-28	N-Monohydroxypropylamide, N-Dihydroxypropylamide und deren Acetonoide der all-E- und 13-Z-Retinsäure, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Mittel
DE2843811A1 (de)	1980-04-24	Retinsaeure- und 7,8-dehydro-retinsaeure-n-(carboxy)-phenylamide
DE2947775C2 (da)	1987-08-27
DE4242396C2 (de)	1995-01-05	Aralkyldiaminderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
DE2749214C2 (da)	1987-11-05
DE2455954A1 (de)	1976-08-12	Diaryloxy-imidazolyl-o,n-acetale, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
DE2822326A1 (de)	1979-11-29	Antimykotische mittel
DE2549798A1 (de)	1977-05-18	Neue imidazolderivate und verfahren zu deren herstellung sowie diese enthaltende arzneimittel
DE2742175A1 (de)	1979-03-29	Antimikrobielle mittel
DE2263817A1 (de)	1973-07-05	Organische verbindungen
DE3126818A1 (de)	1983-01-27	N-(3-(4'-tert.-butyl-cyclohexen-3'-yl)-2-methyl-propyl-1)-cycloalkylamine, verfahren zu ihrer herstellung und diese enthaltende antimykotische mittel
DE2031360A1 (de)	1971-01-21	Neue cyclische Verbindungen und Ver fahren zu ihrer Herstellung
DE2139085A1 (de)	1973-02-15	Halogenierte 4,4-diphenyl-piperidine, verfahren zu deren herstellung und sie enthaltende arzneimittel
DE2749221A1 (de)	1978-06-01	Anilidderivate, verfahren zu ihrer herstellung, verwendung derselben und diese enthaltende arzneimittel
DE3736773A1 (de)	1989-05-11	3-(4-chlorphenyl)-2,2-dimethyl-3-hydroxy-4- (1,2,4-triazol-1-yl)-butyronitril
EP0048828A1 (de)	1982-04-07	Substituierte 2,4-Dichlorphenyl-imidazolyl-vinyl-carbinole, Verfahren zu ihrer Herstellung sowie antimikrobielle Mittel, die diese Stoffe enthalten