GB639854A - Improvements in or relating to the purification of pteridines - Google Patents

Improvements in or relating to the purification of pteridines

Info

Publication number
GB639854A
GB639854A GB13771/47A GB1377147A GB639854A GB 639854 A GB639854 A GB 639854A GB 13771/47 A GB13771/47 A GB 13771/47A GB 1377147 A GB1377147 A GB 1377147A GB 639854 A GB639854 A GB 639854A
Authority
GB
United Kingdom
Prior art keywords
magnesium
solution
water
magnesium salt
pteridine
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
GB13771/47A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB639854A publication Critical patent/GB639854A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/06Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4
    • C07D475/08Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4 with a nitrogen atom directly attached in position 2
    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/02Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
    • C07D475/04Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4 with a nitrogen atom directly attached in position 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (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)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

A reaction mixture containing a pteridine of the formula< <FORM:0639854/IV (b)/1> wherein OH represents an amide group derived from the amino group of glutamic acid or more than one molecule of glutamic acid joined by peptide linkages, is treated with magnesium carbonate, oxide or hydroxide in the presence of water, and the aqueous solution containing the magnesium salt of the above pteridine is separated from the insoluble matter. A water-soluble compound of a metal other than magnesium may be first added to the reaction mixture in the presence of water, the aqueous solution of the metal salt is separated from the insoluble matter and is treated with a water-soluble magnesium compound to form the magnesium salt of the above pteridine by double decomposition. The solution of the magnesium salt may be a hot concentrated solution so that the magnesium salt precipitates out on cooling, e.g. in the case of folic acid itself, the temperature of the solution may be between 75 DEG and 100 DEG C. When the solution contains the magnesium salt of folic acid, the free acid may be precipitated by acidifying the solution to about pH 3. In the examples, magnesium folate is prepared from reaction mixtures containing pteridines, and is converted to folic acid.
GB13771/47A 1946-08-13 1947-05-22 Improvements in or relating to the purification of pteridines Expired GB639854A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US639854XA 1946-08-13 1946-08-13

Publications (1)

Publication Number Publication Date
GB639854A true GB639854A (en) 1950-07-05

Family

ID=22052776

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13771/47A Expired GB639854A (en) 1946-08-13 1947-05-22 Improvements in or relating to the purification of pteridines

Country Status (1)

Country Link
GB (1) GB639854A (en)

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