GB308831A - Process for the manufacture of hydroxy phenoxy quinoline compounds and derivatives and substitution products thereof - Google Patents

Process for the manufacture of hydroxy phenoxy quinoline compounds and derivatives and substitution products thereof

Info

Publication number
GB308831A
GB308831A GB10037/29A GB1003729A GB308831A GB 308831 A GB308831 A GB 308831A GB 10037/29 A GB10037/29 A GB 10037/29A GB 1003729 A GB1003729 A GB 1003729A GB 308831 A GB308831 A GB 308831A
Authority
GB
United Kingdom
Prior art keywords
chloro
methylquinoline
derivatives
manufacture
substitution products
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
GB10037/29A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB308831A publication Critical patent/GB308831A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/20—Oxygen atoms
    • C07D215/22—Oxygen atoms attached in position 2 or 4
    • C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/20—Oxygen atoms
    • C07D215/24—Oxygen atoms attached in position 8
    • C07D215/26—Alcohols; Ethers thereof

Landscapes

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

Abstract

308,831. 1. G. Farbenindustrie Akt.- Ges. March 31, M'<2>8, [Convention date]. V'oid [Published under Sect. 91 of the Acts]. Hydroxyphenoxyquiline compounds are prepared by condensing a quinoline compound containing a reactive group, such as halogen, in the 2- or 4-position with an a.romatie poly hydroxy conipound, if desired in the presence of a solvent. The products are useful thefrapeuticaJly. Examples are given of the interaction in nitrobenzene solution of (1) 2-chloro-4-methylquinoline and resorcinol, pyrogallol or hydroquinone, (2) 2: 8-dichloro-4-methylquinoline, 2-chloro-4- methyl-6-ethoxyquinoline, 2-chloro-4: 5-dimethyl- 8-methosyquinoline and 2-chloro-4-methylquinoline with resorcinol.
GB10037/29A 1928-03-31 1929-03-28 Process for the manufacture of hydroxy phenoxy quinoline compounds and derivatives and substitution products thereof Expired GB308831A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE308831X 1928-03-31

Publications (1)

Publication Number Publication Date
GB308831A true GB308831A (en) 1930-09-29

Family

ID=6121840

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10037/29A Expired GB308831A (en) 1928-03-31 1929-03-28 Process for the manufacture of hydroxy phenoxy quinoline compounds and derivatives and substitution products thereof

Country Status (1)

Country Link
GB (1) GB308831A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0098751A2 (en) * 1979-11-19 1984-01-18 Ici Australia Limited Quinolinyloxy(amino)phenols and alkoxyphenyloxy(amino)quinolines

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0098751A2 (en) * 1979-11-19 1984-01-18 Ici Australia Limited Quinolinyloxy(amino)phenols and alkoxyphenyloxy(amino)quinolines
EP0098751A3 (en) * 1979-11-19 1984-02-22 Ici Australia Limited Quinolinyloxy(amino)phenols and alkoxyphenyloxy(amino)quinolines

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