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GB1037640A - 6,7-dihydro-5h-pyrrolo[3,4-d]pyrimidines - Google Patents

6,7-dihydro-5h-pyrrolo[3,4-d]pyrimidines

Info

Publication number
GB1037640A
GB1037640A GB32308/64A GB3230864A GB1037640A GB 1037640 A GB1037640 A GB 1037640A GB 32308/64 A GB32308/64 A GB 32308/64A GB 3230864 A GB3230864 A GB 3230864A GB 1037640 A GB1037640 A GB 1037640A
Authority
GB
United Kingdom
Prior art keywords
formula
group
general formula
alkyl group
salt
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
GB32308/64A
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.)
Boehringer Ingelheim Pharma GmbH and Co KG
Original Assignee
Dr Karl Thomae GmbH
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 Dr Karl Thomae GmbH filed Critical Dr Karl Thomae GmbH
Publication of GB1037640A publication Critical patent/GB1037640A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim

Landscapes

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

Abstract

The invention comprises compounds of the general formula <FORM:1037640/C2/1> in which R1 is a straight or branched chain alkyl, alkenyl or aralkyl group, R2 is a hydrogen atom or an alkyl group, and R3 is a straight or branched chain alkyl group, an aryl group, an aralkyl group or an alkylthio group, or a group of the formula -NR4R5 in which R4 and R5 are hydrogen atoms or, together with the adjacent nitrogen atom, form a saturated heterocyclic group which may be interrupted by an oxygen atom, and their non-toxic salts with acids and bases, and the preparation thereof by reaction of a pyrrolidone ester formula <FORM:1037640/C2/2> (in which Alk is a lower alkyl group) with a compound of the general formula <FORM:1037640/C2/3> in the presence of a solvent, optionally using the acid addition salts of the last two compounds above in the presence of an acid binding agent, or reacting the alkali metal salt of the pyrrolidone ester of the above formula with the acid addition salt of the amidine of the above formula. The above process may be modified in that the pyrrolidone ester of the third general formula above is prepared by the Dieckmann condensation of a diester of the formula <FORM:1037640/C2/4> wherein n is 0 or 1 or m is 1 or 2 provided (m + n) is 2. Pharmaceutical compositions having antipyretic, antiphlogistic, analgesic, sedative, cardiovascular and/or cytostatic activity, in conventional form for oral, rectal, or parenteral administration, comprise a compound of the first general formula above or a salt thereof and a pharmaceutical carrier or excipient.
GB32308/64A 1963-08-07 1964-08-07 6,7-dihydro-5h-pyrrolo[3,4-d]pyrimidines Expired GB1037640A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DET0024444 1963-08-07

Publications (1)

Publication Number Publication Date
GB1037640A true GB1037640A (en) 1966-08-03

Family

ID=7551453

Family Applications (1)

Application Number Title Priority Date Filing Date
GB32308/64A Expired GB1037640A (en) 1963-08-07 1964-08-07 6,7-dihydro-5h-pyrrolo[3,4-d]pyrimidines

Country Status (4)

Country Link
CH (1) CH431550A (en)
DE (1) DE1470345A1 (en)
FR (1) FR4087M (en)
GB (1) GB1037640A (en)

Also Published As

Publication number Publication date
CH431550A (en) 1967-03-15
DE1470345A1 (en) 1969-12-04
FR4087M (en) 1966-04-18

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