GB1268239A - Tricycloundecane derivatives - Google Patents
Tricycloundecane derivativesInfo
- Publication number
- GB1268239A GB1268239A GB44373/69A GB4437369A GB1268239A GB 1268239 A GB1268239 A GB 1268239A GB 44373/69 A GB44373/69 A GB 44373/69A GB 4437369 A GB4437369 A GB 4437369A GB 1268239 A GB1268239 A GB 1268239A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- tricyclo
- reaction
- methyl
- undecane
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
- C07D303/06—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms in which the oxirane rings are condensed with a carbocyclic ring system having three or more relevant rings
-
- 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
- A61P31/12—Antivirals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/32—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
- C07C1/34—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen reacting phosphines with aldehydes or ketones, e.g. Wittig reaction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/29—Saturated compounds containing keto groups bound to rings
- C07C49/313—Saturated compounds containing keto groups bound to rings polycyclic
- C07C49/323—Saturated compounds containing keto groups bound to rings polycyclic having keto groups bound to condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/417—Saturated compounds containing a keto group being part of a ring polycyclic
- C07C49/423—Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system
- C07C49/453—Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system having three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/12—Saturated polycyclic compounds
- C07C61/125—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system
- C07C61/135—Saturated polycyclic compounds having a carboxyl group bound to a condensed ring system having three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/76—Ring systems containing bridged rings containing three rings containing at least one ring with more than six ring members
- C07C2603/78—Ring systems containing bridged rings containing three rings containing at least one ring with more than six ring members containing seven-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
1,268,239. Tricycloundecane derivatives. E.I. DU PONT DE NEMOURS & CO. 8 Sept., 1969 [9 Sept., 1968; 31 July, 1969], No. 44373/69. Heading C2C. [Also in Division C5] Novel compounds I in which Q has Formula II n is 0 or 1; R<SP>1</SP> and R<SP>2</SP> are H or 1-2C alkyl; R 3 is H, 1-4C alkyl, 3-9C alkenyl, 3-methyl-2- methylene - 3 - butenyl, 5-8C cycloalkenyl, 6-9C alkenylcycloalkyl, 6-9C cycloalkylalkenyl, 3-5C alkynyl, or benzyl and R 4 is H, 1-3C alkyl, 3-5C alkenyl or propargyl or R 3 and R 4 together form a divalent organic radical subject to the proviso that any unsaturation in R 3 and R 4 is not in the 1-position and salts thereof are prepared by (a) reducing compounds III in which A is a group capable of being reduced to NH 2 or -CH(R<SP>2</SP>)NH 2 ; (b) reductively aminating a compound III in which A is a group or atom capable of being reductively aminated to a group (c) reductively aminating with NH 3 tricycloundecan-4-ane to give I where n is 0 and R 1 , R 3 and R 4 are all H (d) reacting a compound IV where X is a leaving group with an amine donor (e) reducing a compound V where R<SP>4</SP> and R<SP>5</SP> are H or 1-3C alkyl (f) converting the amino group in I into a different amino group by known methods or (g) hydrolysing a compound VI Spiro[ozirane - 2,2<SP>1</SP>-tricyclo(3.3.1.1<SP>3,7</SP>)]-decane is prepared by oxidation of 2-methyleneadamantane. Adamantane cyanohydrin is prepared by reaction of adamantanone with NaCN. 2 - Aminomethyl - 2 - adamantanol is prepared by reaction of adamantane cyanohydrin with LiAlH 4 or by reaction of the above spiro intermediate with NH 3 in a stainless steel bomb. Novel tricyclo(4.3.1.1.<SP>3,8</SP>)undecan-4-one is prepared by reaction of 2-amino-methyl-2-adamantanol with NaNO 2 and glacial acetic acid. Tricyclo(4.3.1.1.<SP>3,8</SP>)undecan - 4 - one - oxime is prepared by reaction of the 4-one with hydroxylamine HCl. 4 - Formamido - tricyclo(4.3.1.1<SP>3,8</SP>) - undecane is prepared by reaction of the appropriate 4- amino compound with butyl formate. Similarly prepared are 4-formamidomethyl-; 4-methyl-4- formamidomethyl; α - methyl - 4 - formamidomethyl- and N - formyl - N - methyl - 4 - aminomethyl-tricyclo(4.3.1.1.<SP>3,8</SP>)-undecane. N - acetyl - tricyclo(4.3.1.1<SP>3,8</SP>)undecane - 4- amine is prepared by acetylation of the appropriate amine. Similarly prepared are N-acetyl- N - methyl - 4 - amino- ; N - acetyl - N - methyl- 4 - amino - methyl-; N - acetyl - α - methyl - 4- aminomethyl-; N - acetyl N - methyl - 4 - amino- 4 - ethyl-; N - acetyl - N - benzyl - 4 - aminomethyl- and N - acetyl - N - (3 - cyclohexenyl)- 4 - aminomethyl - tricyclo(4.3.1.1.<SP>3,8</SP>) - undecane. 4 - Ethyl - 4 - hydroxy - tricyclo(4.3.1.1<SP>3,8</SP>)- undecane is prepared by reaction of the 4-one with ethyl lithium. The 4-methyl derivative may be similarly prepared. Tricyclo(4.3.1.1.<SP>3,8</SP>)undecan - 4 - ol is prepared by reduction of the 4-one with LiAlH 4 . 4 . Bromo - tricyclo(4.3.1.1<SP>3,8</SP>)undecane is prepared by reaction of the 4-ol with Br 2 . 4 - Methylene - tricyclo(4.3.1.1<SP>3,8</SP>)undecane is prepared by reaction of the 4-one with methyl triphenylphosphonium bromide. 4 - Hydroxymethyl - tricyclo(4.3.1.1<SP>3,8</SP>)undecane is prepared from the 4-methylene derivative by reaction with H 2 O 2 . Tricyclo(4.3.1.1<SP>3,8</SP>)undecane - 4 - carboxylic acid is prepared by oxidation of the 4-hydroxymethyl derivative. The corresponding acid chloride is prepared by conventional methods and converted to the 4-carboxamide by reaction with NH 3 . Similarly prepared are the N-allyl-; N - (1,1 - dimethylallyl)-; N - (3 - methylenecyclobutylmethyl)-; N - (2 - methallyl)- and N- (3 methylenecyclobutyl) - carboxamide derivatives and 3 - methylene - 1 - [tricyclo(4.3.1.1.<SP>3,8</SP>)undecan - 4 - yl . carbonyl] - azetidine. 4 - Cyano - tricyclo(4.3.1.1<SP>3,8</SP>) - undecane is prepared by reaction of the 4-carboxamide derivative with SOCl 2 or by reaction of the 4- bromo derivative with NaCN. Methyl - 4 - tricyclo(4.3.1.1.<SP>3,8</SP>)undecyl ketone is prepared by reaction of the 4 cyano derivative with methyl magnesium bromide. Pharmaceutical compositions comprise a compound I together with a suitable excipient for oral or parenteral administration as anti-viral agents.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75863168A | 1968-09-09 | 1968-09-09 | |
US84662069A | 1969-07-31 | 1969-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1268239A true GB1268239A (en) | 1972-03-22 |
Family
ID=27116551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44373/69A Expired GB1268239A (en) | 1968-09-09 | 1969-09-08 | Tricycloundecane derivatives |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS4813539B1 (en) |
BR (1) | BR6912297D0 (en) |
CH (1) | CH529083A (en) |
DE (1) | DE1945208A1 (en) |
FR (1) | FR2017657B1 (en) |
GB (1) | GB1268239A (en) |
NL (1) | NL6913643A (en) |
SE (1) | SE373358B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2529025C1 (en) * | 2013-04-23 | 2014-09-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Method of producing 2,2-adamantylene spirooxirane derivatives |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2202877B1 (en) * | 1972-10-11 | 1980-02-08 | Nippon Zeon Co | |
JPS5273035A (en) * | 1975-12-15 | 1977-06-18 | Asahi Kagaku Kenkyusho | Device for regenerating fixer |
DE2749664B2 (en) * | 1977-11-05 | 1981-01-29 | Kloeckner-Werke Ag, 4100 Duisburg | Connecting and securing device for the chain conveyor with or without guides for mining machines, in particular for coal |
DE3314499C2 (en) * | 1983-04-21 | 1985-08-22 | Hermann Hemscheidt Maschinenfabrik Gmbh & Co, 5600 Wuppertal | Access device for a longwall |
AU4879785A (en) * | 1984-10-19 | 1986-04-24 | E.I. Du Pont De Nemours And Company | Preparing rimantadine |
DE3511494A1 (en) * | 1985-03-29 | 1986-10-09 | Saarbergwerke AG, 6600 Saarbrücken | Joint-bridging connection of channel elements of scraper conveyors or their fittings |
DE20307151U1 (en) | 2003-05-07 | 2004-07-22 | Dbt Gmbh | Gag for gag connections and gag connection |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1054275A (en) * | 1963-05-01 | |||
CH429709A (en) * | 1964-03-26 | 1967-02-15 | Geigy Ag J R | Process for the preparation of a new tricycloalkanamine |
-
1969
- 1969-09-05 CH CH1351069A patent/CH529083A/en not_active IP Right Cessation
- 1969-09-06 DE DE19691945208 patent/DE1945208A1/en active Pending
- 1969-09-08 NL NL6913643A patent/NL6913643A/xx unknown
- 1969-09-08 JP JP44070639A patent/JPS4813539B1/ja active Pending
- 1969-09-08 GB GB44373/69A patent/GB1268239A/en not_active Expired
- 1969-09-08 SE SE6912363A patent/SE373358B/en unknown
- 1969-09-09 FR FR696930581A patent/FR2017657B1/fr not_active Expired
- 1969-09-09 BR BR212297/69A patent/BR6912297D0/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2529025C1 (en) * | 2013-04-23 | 2014-09-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Method of producing 2,2-adamantylene spirooxirane derivatives |
Also Published As
Publication number | Publication date |
---|---|
NL6913643A (en) | 1970-03-11 |
CH529083A (en) | 1972-10-15 |
BR6912297D0 (en) | 1973-05-10 |
FR2017657A1 (en) | 1970-05-22 |
FR2017657B1 (en) | 1973-06-08 |
SE373358B (en) | 1975-02-03 |
DE1945208A1 (en) | 1970-03-19 |
JPS4813539B1 (en) | 1973-04-27 |
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