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GB539893A - Improvements in the preparation of water-soluble derivatives of 2-sulfanilylamidopyridine - Google Patents

Improvements in the preparation of water-soluble derivatives of 2-sulfanilylamidopyridine

Info

Publication number
GB539893A
GB539893A GB5168/40A GB516840A GB539893A GB 539893 A GB539893 A GB 539893A GB 5168/40 A GB5168/40 A GB 5168/40A GB 516840 A GB516840 A GB 516840A GB 539893 A GB539893 A GB 539893A
Authority
GB
United Kingdom
Prior art keywords
compound
water
sodium
disodium
treatment
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
GB5168/40A
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.)
Merck and Co Inc
Original Assignee
Merck 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 Merck and Co Inc filed Critical Merck and Co Inc
Publication of GB539893A publication Critical patent/GB539893A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/76Nitrogen atoms to which a second hetero atom is attached

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

539,893. Sulphonamido compounds. MERCK & CO., Inc. March 20, 1940, No. 5168. Convention date, March 23, 1939. [Class 2 (iii)] 2 - p - Aminobenzenesulphonamidopyridine, described in Specification 512,145, is converted into its water-soluble N-sodium methylenesulphinate bv treatment with sodium formaldehyde-sulphoxylate in water, glycerine or an aliphatic alcohol or glycol as solvent. The water-soluble disodium compound is obtained if the starting material is used in the form of its sodium compound ; treatment of the disodium compound with mineral acid gives rise to the monosodium compound, from which the disodium compound can be regenerated with caustic soda. The free methylenesulphinic acid may be prepared from the disodium compound by treatment with acetic acid. The products are useful therapeutically. An example is given of the preparation of the monosodium compound, i.e. the N-sodium methylenesulphinate.
GB5168/40A 1939-03-23 1940-03-20 Improvements in the preparation of water-soluble derivatives of 2-sulfanilylamidopyridine Expired GB539893A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US539893XA 1939-03-23 1939-03-23

Publications (1)

Publication Number Publication Date
GB539893A true GB539893A (en) 1941-09-29

Family

ID=21987953

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5168/40A Expired GB539893A (en) 1939-03-23 1940-03-20 Improvements in the preparation of water-soluble derivatives of 2-sulfanilylamidopyridine

Country Status (1)

Country Link
GB (1) GB539893A (en)

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