GB1231380A - - Google Patents

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Publication number
GB1231380A
GB1231380A GB1231380DA GB1231380A GB 1231380 A GB1231380 A GB 1231380A GB 1231380D A GB1231380D A GB 1231380DA GB 1231380 A GB1231380 A GB 1231380A
Authority
GB
United Kingdom
Prior art keywords
azabicyclo
octan
trimethyl
iii
give
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
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 filed Critical
Publication of GB1231380A publication Critical patent/GB1231380A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/06Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing isoquinuclidine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

1,231,380. Isoquinuclidine derivatives. COMMISSARIAT A L'ENERGIE ATOMIQUE. 24 Sept., 1969 [7 Oct., 1968], No. 47063/69. Heading C2C. Isoquinuclidine - (2 - azabicyclo - [2.2.2]- octane) derivatives are prepared by reacting where R, R<SP>1</SP> and R<SP>11</SP> are organic radicals, with ammonia. In examples, piperitenone (R=R<SP>1</SP> = R<SP>11</SP>=CH 3 ) is thus converted to 1,3,3-trimethyl- 2 - azabicyclo - [2.2.2] - octan - 5 - one (I) which is in turn reacted with the acetic anhydride in pyridine to give N-acetyl-1,3,3-trfinethyl-2- azabicyclo-[2.2.2]-octan-5-one and the compound of formula and with LiAlH 4 to give 1,3,3-trimethyl-2- azabicyclo - (2.2.2) - octan - 5 - ol (III). Compounds (I) and (III) are converted to the corresponding nitroxide free radicals by means of H 2 O 2 /phosphotungstic acid.
GB1231380D 1968-10-07 1969-09-24 Expired GB1231380A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR169028 1968-10-07

Publications (1)

Publication Number Publication Date
GB1231380A true GB1231380A (en) 1971-05-12

Family

ID=8655369

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1231380D Expired GB1231380A (en) 1968-10-07 1969-09-24

Country Status (3)

Country Link
CH (1) CH513870A (en)
FR (1) FR1591639A (en)
GB (1) GB1231380A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3875169A (en) * 1973-12-28 1975-04-01 Ciba Geigy Corp Bicyclic hindered amines
US3879396A (en) * 1973-12-28 1975-04-22 Ciba Geigy Corp Bicyclic hindered amino acids and metal salts thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3875169A (en) * 1973-12-28 1975-04-01 Ciba Geigy Corp Bicyclic hindered amines
US3879396A (en) * 1973-12-28 1975-04-22 Ciba Geigy Corp Bicyclic hindered amino acids and metal salts thereof

Also Published As

Publication number Publication date
CH513870A (en) 1971-10-15
FR1591639A (en) 1970-05-04

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Legal Events

Date Code Title Description
PS Patent sealed
435 Patent endorsed 'licences of right' on the date specified (sect. 35/1949)
PLNP Patent lapsed through nonpayment of renewal fees