GB1006385A - Isopropanols and the manufacture thereof - Google Patents

Isopropanols and the manufacture thereof

Info

Publication number
GB1006385A
GB1006385A GB11160/64A GB1116064A GB1006385A GB 1006385 A GB1006385 A GB 1006385A GB 11160/64 A GB11160/64 A GB 11160/64A GB 1116064 A GB1116064 A GB 1116064A GB 1006385 A GB1006385 A GB 1006385A
Authority
GB
United Kingdom
Prior art keywords
pyridyl
methyl
alkoxy
methane
halogen atom
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
GB11160/64A
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of GB1006385A publication Critical patent/GB1006385A/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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention comprises compounds of the general formula <FORM:1006385/C2/1> wherein the symbol S represents substitution comprising a halogen atom or an alkyl, alkoxy or alkyl mercapto group or three alkoxy groups and the broken line denotes that such substitution is optional, and acid addition salts thereof; and the preparation thereof by reacting a (pyridyl-(4)-methyl)-alkali metal or -magnesium halide derivative with a compound of the formula <FORM:1006385/C2/2> wherein R represents a halogen atom or an alkoxy, benzyloxy or phenoxy group and S and the broken line have the significance given above and, if desired, converting the reaction product into an acid addition salt. [Pyridyl - (4) - methyl] - lithium is prepared by the interaction of pyridyl-(4)-methane and phenyl lithium in an ether benzene solution under an atmosphere of dry nitrogen. [Pyridyl - (4) - methyl] - magnesium bromide is prepared by the reaction of pyridyl-(4)-methane and ethyl magnesium bromide in tetrahydro-furan solution under reflux conditions. Pharmaceutical compositions for use as anti-parkinson agents when administered enterally or parenterally comprising the compound of the first general formula above and an inert diluent or exipient. The composition may be in the form of tablets, dragees, suppositories, capsules, solutions, emulsions or suspensions.
GB11160/64A 1963-03-18 1964-03-17 Isopropanols and the manufacture thereof Expired GB1006385A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US26602963A 1963-03-18 1963-03-18

Publications (1)

Publication Number Publication Date
GB1006385A true GB1006385A (en) 1965-09-29

Family

ID=23012875

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11160/64A Expired GB1006385A (en) 1963-03-18 1964-03-17 Isopropanols and the manufacture thereof

Country Status (9)

Country Link
BE (1) BE645241A (en)
BR (1) BR6457623D0 (en)
CH (1) CH453357A (en)
DE (1) DE1445891A1 (en)
DK (1) DK112656B (en)
ES (1) ES297720A1 (en)
FR (2) FR3260M (en)
GB (1) GB1006385A (en)
NL (1) NL6402889A (en)

Also Published As

Publication number Publication date
BR6457623D0 (en) 1973-07-17
DK112656B (en) 1969-01-06
CH453357A (en) 1968-06-14
DE1445891A1 (en) 1968-11-28
BE645241A (en) 1964-09-16
NL6402889A (en) 1964-09-21
ES297720A1 (en) 1964-09-01
FR1397328A (en) 1965-04-30
FR3260M (en) 1965-04-20

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