ES267045A1 - New dialkyl xanthine derivatives and the preparation thereof - Google Patents

New dialkyl xanthine derivatives and the preparation thereof

Info

Publication number
ES267045A1
ES267045A1 ES0267045A ES267045A ES267045A1 ES 267045 A1 ES267045 A1 ES 267045A1 ES 0267045 A ES0267045 A ES 0267045A ES 267045 A ES267045 A ES 267045A ES 267045 A1 ES267045 A1 ES 267045A1
Authority
ES
Spain
Prior art keywords
preparation
reacted
solutions
compounds
appropriate
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
ES0267045A
Other languages
Spanish (es)
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.)
Aens SA Manufacture De Produit
Original Assignee
Aens SA Manufacture De Produit
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 Aens SA Manufacture De Produit filed Critical Aens SA Manufacture De Produit
Publication of ES267045A1 publication Critical patent/ES267045A1/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention comprises compounds of general formula: <FORM:0947496/C2/1> in which R1 and R2 represent alkyl radicals, X represents an alkylene radical, R3 and R3 represent hydrogen atoms or aralkyl (e.g. furfuryl) alkyl or alkenyl groups, or R3 is hydrogen and R4 is a cycloalkyl, dialkylaminoalkyl, alkoxyalkyl or heterocyclic radical, or R3 and R4 together form a heterocyclic ring which may be substituted and their acid addition salts and processes for the preparation thereof wherein (1) an appropriate 7-haloalkylxanthine is reacted with a compound HNR3R4, or (2) an appropriate 7-unsubstituted xanthine is reacted with a compound Hal.X.NR3R4, Hal being a halogen atom. Pharmaceutical compositions comprise an acceptable carrier or diluent together with the above compounds. Forms suitable for oral (tablets, capsules, solutions, suspensions), parenteral (solutions) and rectal (suppositories) administration are mentioned. The compounds stimulate the central nervous system, and have spasmolytic action on smooth muscles and a positive inotropic action on the heart. Specification 947,494 is referred to.
ES0267045A 1960-05-03 1961-05-02 New dialkyl xanthine derivatives and the preparation thereof Expired ES267045A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB15617/60A GB947496A (en) 1960-05-03 1960-05-03 New dialkyl xanthine derivatives and the preparation thereof

Publications (1)

Publication Number Publication Date
ES267045A1 true ES267045A1 (en) 1961-12-01

Family

ID=10062377

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0267045A Expired ES267045A1 (en) 1960-05-03 1961-05-02 New dialkyl xanthine derivatives and the preparation thereof

Country Status (6)

Country Link
BE (1) BE603114A (en)
DE (1) DE1246744B (en)
ES (1) ES267045A1 (en)
FR (1) FR1357M (en)
GB (1) GB947496A (en)
LU (1) LU40076A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0011399A1 (en) * 1978-11-11 1980-05-28 FISONS plc N-substituted theophyllines, processes for their preparation and pharmaceutical compositions containing them

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1011424B (en) * 1954-04-17 1957-07-04 Chemiewerk Homburg Ag Process for the preparation of basic substituted 7-alkyl-xanthine derivatives or their salts
US2887486A (en) * 1956-10-29 1959-05-19 S E Massengill Company Theophylline derivatives

Also Published As

Publication number Publication date
LU40076A1 (en) 1961-10-30
DE1246744B (en) 1967-08-10
BE603114A (en) 1961-10-27
GB947496A (en) 1964-01-22
FR1357M (en) 1962-06-18

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