GB1142029A - Optically active substituted piperidines and process for their manufacture - Google Patents

Optically active substituted piperidines and process for their manufacture

Info

Publication number
GB1142029A
GB1142029A GB2642366A GB2642366A GB1142029A GB 1142029 A GB1142029 A GB 1142029A GB 2642366 A GB2642366 A GB 2642366A GB 2642366 A GB2642366 A GB 2642366A GB 1142029 A GB1142029 A GB 1142029A
Authority
GB
United Kingdom
Prior art keywords
optically active
phenyl
substituted
piperidine
substituted piperidine
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
GB2642366A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB1142029A publication Critical patent/GB1142029A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/10Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
    • C07D211/14Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

1,142,029. Substituted piperidines. CIBA Ltd. 14 June, 1966 [14 June, 1965], No. 26423/66. Heading C2C. Novel substituted piperidines of the general formula wherein Ph 1 and Ph 2 each stands for a phenyl, lower alkyl-phenyl, lower alkoxy-phenyl or halo-phenyl group and X stands for a hydroxy group or a halogen atom, especially a chlorine atom, and acid addition salts thereof, are prepared by (a) resolving the racemic substituted piperidine with an optically active acid, (b) replacing the amino group in an optically active 1.(#-aminoetbyl) substituted piperidine by a hydroxyl group or a halogen atom, (c) adding water or a hydrohalide to an optically active 1-vinyl substituted piperidine, and (d) reacting an optically active N-unsubstituted piperidine with ethylene oxide or a reactive monoester of ethylene glycol; followed by optional saltformation. Pharmaceutical compositions having gastric secretion inhibiting, antitremorine and stimulating activity comprise as active ingredient a substituted piperidine of the above general formula or a physiologically tolerable acid addition salt thereof and a pharmaceutically suitable carrier.
GB2642366A 1965-06-14 1966-06-14 Optically active substituted piperidines and process for their manufacture Expired GB1142029A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US46384865A 1965-06-14 1965-06-14
US53109466A 1966-03-02 1966-03-02

Publications (1)

Publication Number Publication Date
GB1142029A true GB1142029A (en) 1969-02-05

Family

ID=27040762

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2642366A Expired GB1142029A (en) 1965-06-14 1966-06-14 Optically active substituted piperidines and process for their manufacture

Country Status (5)

Country Link
AT (2) AT265267B (en)
BE (1) BE682430A (en)
ES (1) ES327880A1 (en)
GB (1) GB1142029A (en)
NL (1) NL6608186A (en)

Also Published As

Publication number Publication date
ES327880A1 (en) 1967-08-01
BE682430A (en) 1966-12-13
NL6608186A (en) 1966-12-15
AT265267B (en) 1968-10-10
AT265264B (en) 1968-10-10

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