GB682691A - Manufacture of therapeutically active salts of camphor sulphonic acids - Google Patents

Manufacture of therapeutically active salts of camphor sulphonic acids

Info

Publication number
GB682691A
GB682691A GB33178/49A GB3317849A GB682691A GB 682691 A GB682691 A GB 682691A GB 33178/49 A GB33178/49 A GB 33178/49A GB 3317849 A GB3317849 A GB 3317849A GB 682691 A GB682691 A GB 682691A
Authority
GB
United Kingdom
Prior art keywords
camphor
salt
acid
reacting
base
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
GB33178/49A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of GB682691A publication Critical patent/GB682691A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/32Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of salts of sulfonic acids

Landscapes

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

Abstract

Salts of non-halogenated comphorsulphonic acids (active and racemic) with 1-phenyl and 1-monohydroxyphenyl-2-aminoethanols and N-alkyl derivatives thereof (l- and dl-forms) are prepared by (1) reacting the base with the acid, (2) reacting a salt of the base with a salt of the acid, or (3) reacting the corresponding aryl aminomethyl ketone with the camphorsulphonic acid and reducing the product to the aminoethanol salt. In method (3), reduction is carried out by catalytic hydrogenation in aqueous solution at ordinary temperatures using palladium or nickel. The salt of the ketone may be made by direct neutralization or double decomposition. Examples show the reaction (1) l-l-(m-hydroxyphenyl)-2-methylamino-ethanol with d-camphor-b -sulphonic acid, (2) the same base with dl-camphor-a -sulphonic acid and (3) dl-l-(p-hydroxyphenyl)-2-aminoethanol hydrochloride with sodium dl-camphor-b -sulphonate. A further example describes the preparation of phenyl aminomethyl camphor-p -sulphonate and hydrogenation of the product. The Specification as open to inspection under Sect. 91 referes in general to the preparation of camphorsulphonates of aromatic ethanolamines and ethanolalkylamines, and to therapeutic compositions containing such salts. This subject-matter does not appear in the Specification as accepted.
GB33178/49A 1948-12-31 1949-12-29 Manufacture of therapeutically active salts of camphor sulphonic acids Expired GB682691A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US682691XA 1948-12-31 1948-12-31

Publications (1)

Publication Number Publication Date
GB682691A true GB682691A (en) 1952-11-12

Family

ID=22081492

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33178/49A Expired GB682691A (en) 1948-12-31 1949-12-29 Manufacture of therapeutically active salts of camphor sulphonic acids

Country Status (1)

Country Link
GB (1) GB682691A (en)

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