GB853799A - Diquaternary compounds and process of preparing same - Google Patents

Diquaternary compounds and process of preparing same

Info

Publication number
GB853799A
GB853799A GB40294/57A GB4029457A GB853799A GB 853799 A GB853799 A GB 853799A GB 40294/57 A GB40294/57 A GB 40294/57A GB 4029457 A GB4029457 A GB 4029457A GB 853799 A GB853799 A GB 853799A
Authority
GB
United Kingdom
Prior art keywords
alkyl
group
benzyl
groups
substituted
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
Application number
GB40294/57A
Inventor
Ellis Rex Pinson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Inc
Original Assignee
Pfizer Inc
Charles Pfizer and Co Inc
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
Application filed by Pfizer Inc, Charles Pfizer and Co Inc filed Critical Pfizer Inc
Publication of GB853799A publication Critical patent/GB853799A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic 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
    • C07D295/02Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/06Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2603/10Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • C07C2603/12Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
    • C07C2603/18Fluorenes; Hydrogenated fluorenes

Abstract

The invention comprises compounds of the general formula: <FORM:0853799/IV(b)/1> wherein Alk is an alkylene group containing 2-5 carbon atoms in the straight chain between the N atom, R1 and R2 are C1-3 alkyl groups or, together with the adjacent nitrogen atom, a heterocyclic ring, R3, R4 and R5 are C1-3 alkyl groups, X is a substituted or unsubstituted benzyl, 1-naphthylmethyl, 1-indanyl or 9-fluorenyl group the said substitutents being in the ring once being one or more halogen atoms. C1-4 alkyl and C1-4 alkoxy groups, or when X is benzyl or 1-naphthymethyl, additionally on the a -carbon atom, and being a C1-4 alkyl group of a substituted or unsubstituted phenyl group wherein the substitutents are the same as those on the phenyl a naphthyl nuceli of the benzyl a 1-naphthyemethyl groups respectively, and A is a pharmacologically acceptable anion, and the preparation thereof by reacting diamines of the general formula: <FORM:0853799/IV(b)/2> wherein R6, R7 and R8 are the same as R1, R2 and R4 except they may additionally be hydrogen atoms. Diamines of formula (II) are prepared by reductive condensation of an diamine and an appropriate (aromatic) aldehyde or ketone; condensation of a diamine with an acid chloride followed by reduction of the amide; or reductive condensation of a primary amine and an aromatic aldehyde or ketone followed by condensation with a dialkyl-amino substituted alkyl halide. An additional alkyl group is introduced by reacting the amine with a carbonyl group in the presence of a reducing agent, for example, formic acid.ALSO:Pharmaceutical compositions comprise as active ingredient compounds of the general formula: <FORM:0853799/VI/1> wherein Alk is an alkylene group containing 2-5C in the straight chain between the N-atoms, R1 and R2 are C1-3 alkyl groups or, together with the adjacent N atom a heterocylic ring, R3, R4 and R5 are C1-3 alkyl groups X is a substituted or unsubstituted benzyl, 1-naphthylmethyl, 1-indanyl, or 9-fluorenyl group, the said substituents being in the ring and being one or more halogen atoms C1-4 alkyl or alkoxy groups, or when X is a benzyl or 1-naphthyl methyl group additionally on the a -carbon atom, and being a C1-4 alkyl group or a phenyl group, optionally substituted as in the benzyl a naphthylmethyl groups above and A is a pharmacologically acceptable organic or inorganic anion, together with a pharmaceutically acceptable carrier. Compositions include tablets, capsules, troches, lozenges or solutions the last named both for oral and parenteral administration.
GB40294/57A 1957-11-21 1957-12-30 Diquaternary compounds and process of preparing same Expired GB853799A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1080563XA 1957-11-21 1957-11-21
US4029457XA 1957-12-30 1957-12-30

Publications (1)

Publication Number Publication Date
GB853799A true GB853799A (en) 1960-11-09

Family

ID=10414171

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40294/57A Expired GB853799A (en) 1957-11-21 1957-12-30 Diquaternary compounds and process of preparing same

Country Status (4)

Country Link
BE (1) BE571158A (en)
DE (1) DE1080563B (en)
FR (1) FR1241122A (en)
GB (1) GB853799A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3225101A (en) * 1962-12-26 1965-12-21 Grace W R & Co Process for purifying hydrazinium chlorides
EP0303181A2 (en) * 1987-08-11 1989-02-15 Roche Diagnostics GmbH 1,2-Diamine compounds, process for their preparation as well as medicaments containing these compounds
US7928123B2 (en) 2006-09-25 2011-04-19 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US7935715B2 (en) 2006-07-28 2011-05-03 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US8048899B2 (en) 2008-09-25 2011-11-01 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8178568B2 (en) 2008-07-10 2012-05-15 Boehringer Ingelheim International Gmbh Sulfone compounds which modulate the CB2 receptor
US8299103B2 (en) 2009-06-15 2012-10-30 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
CN102796511A (en) * 2011-05-27 2012-11-28 中国科学院理化技术研究所 Fluorescent probe for quantitatively detecting heparin, and synthesis method and application thereof
US8329735B2 (en) 2010-03-05 2012-12-11 Boehringer Ingelheim International Gmbh Tetrazole compounds which selectively modulate the CB2 receptor
US8383651B2 (en) 2009-09-22 2013-02-26 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8383615B2 (en) 2009-06-16 2013-02-26 Boehringer Ingelheim International Gmbh Azetidine 2-carboxamide derivatives which modulate the CB2 receptor
US8546563B2 (en) 2007-11-07 2013-10-01 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US8846936B2 (en) 2010-07-22 2014-09-30 Boehringer Ingelheim International Gmbh Sulfonyl compounds which modulate the CB2 receptor
US8865744B1 (en) 2013-05-17 2014-10-21 Boehringer Ingelheim International Gmbh (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US8957063B2 (en) 2008-02-21 2015-02-17 Boehringer Ingelheim International Gmbh Amine and ether compounds which modulate the CB2 receptor
US9315454B2 (en) 2010-01-15 2016-04-19 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1210874B (en) * 1961-12-14 1966-02-17 Degussa Process for the preparation of diarylamino derivatives of arylaminoalkanes
CH328574A4 (en) * 1974-03-08 1975-06-30

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3225101A (en) * 1962-12-26 1965-12-21 Grace W R & Co Process for purifying hydrazinium chlorides
EP0303181A2 (en) * 1987-08-11 1989-02-15 Roche Diagnostics GmbH 1,2-Diamine compounds, process for their preparation as well as medicaments containing these compounds
EP0303181A3 (en) * 1987-08-11 1991-09-04 Roche Diagnostics GmbH 1,2-diamine compounds, process for their preparation as well as medicaments containing these compounds
US8299111B2 (en) 2006-07-28 2012-10-30 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US7935715B2 (en) 2006-07-28 2011-05-03 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US7928123B2 (en) 2006-09-25 2011-04-19 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US8829034B2 (en) 2006-09-25 2014-09-09 Boehringer Ingerlheim International GmbH Compounds which modulate the CB2 receptor
US8546563B2 (en) 2007-11-07 2013-10-01 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US8957063B2 (en) 2008-02-21 2015-02-17 Boehringer Ingelheim International Gmbh Amine and ether compounds which modulate the CB2 receptor
US8178568B2 (en) 2008-07-10 2012-05-15 Boehringer Ingelheim International Gmbh Sulfone compounds which modulate the CB2 receptor
US8048899B2 (en) 2008-09-25 2011-11-01 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8349871B2 (en) 2008-09-25 2013-01-08 Boehringer Ingelheim International Gmbh Therapeutic uses of compounds which selectively modulate the CB2 receptor
US8362039B2 (en) 2008-09-25 2013-01-29 Boehringer Ingelheim International Gmbh Therapeutic uses of compounds which selectively modulate the CB2 receptor
US8372874B2 (en) 2008-09-25 2013-02-12 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8299103B2 (en) 2009-06-15 2012-10-30 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8735430B2 (en) 2009-06-15 2014-05-27 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US8383615B2 (en) 2009-06-16 2013-02-26 Boehringer Ingelheim International Gmbh Azetidine 2-carboxamide derivatives which modulate the CB2 receptor
US8383651B2 (en) 2009-09-22 2013-02-26 Boehringer Ingelheim International Gmbh Compounds which selectively modulate the CB2 receptor
US9315454B2 (en) 2010-01-15 2016-04-19 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
US8329735B2 (en) 2010-03-05 2012-12-11 Boehringer Ingelheim International Gmbh Tetrazole compounds which selectively modulate the CB2 receptor
US8846936B2 (en) 2010-07-22 2014-09-30 Boehringer Ingelheim International Gmbh Sulfonyl compounds which modulate the CB2 receptor
CN102796511A (en) * 2011-05-27 2012-11-28 中国科学院理化技术研究所 Fluorescent probe for quantitatively detecting heparin, and synthesis method and application thereof
US8865744B1 (en) 2013-05-17 2014-10-21 Boehringer Ingelheim International Gmbh (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US9650370B2 (en) 2013-05-17 2017-05-16 Centrexion Therapeutics Corporation (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US10112934B2 (en) 2013-05-17 2018-10-30 Centrexion Therapeutics Corporation (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US10570125B2 (en) 2013-05-17 2020-02-25 Centrexion Therapeutics Corporation (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US11084810B2 (en) 2013-05-17 2021-08-10 Centrexion Therapeutics Corporation (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles
US11725004B2 (en) 2013-05-17 2023-08-15 Centrexion Therapeutics Corporation (Cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles

Also Published As

Publication number Publication date
BE571158A (en) 1959-03-12
FR1241122A (en) 1960-12-20
DE1080563B (en) 1960-04-28

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