ES411407A1 - Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES411407A1
ES411407A1 ES411407A ES411407A ES411407A1 ES 411407 A1 ES411407 A1 ES 411407A1 ES 411407 A ES411407 A ES 411407A ES 411407 A ES411407 A ES 411407A ES 411407 A1 ES411407 A1 ES 411407A1
Authority
ES
Spain
Prior art keywords
radical
general formula
oxazoles
translation
procedure
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
ES411407A
Other languages
Spanish (es)
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.)
Boehringer Ingelheim Pharma GmbH and Co KG
Original Assignee
Dr Karl Thomae GmbH
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 Dr Karl Thomae GmbH filed Critical Dr Karl Thomae GmbH
Priority to ES411407A priority Critical patent/ES411407A1/en
Publication of ES411407A1 publication Critical patent/ES411407A1/en
Expired legal-status Critical Current

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Procedure for the preparation of new oxazoles of the general formula I **(See formula)** in which R means a hydrogen atom, an alcohol radical with 1 to 4 carbon atoms substituted by a hydroxy, carboxy or carbalkoxy group, an aliphatic acyl radical with 1 to 6 carbon atoms, saturated or unsaturated, optionally substituted by a hydroxy group, a benzoyl radical optionally substituted by methyl or methoxy groups or halogen atoms, a pyridinecarbonyl or phenylacetyl radical, and its salts physiologically compatible with organic or inorganic acids, characterized in that a 5-halogen derivative is reacted with urea -azepinone- (4) of the general formula II **(See formula)** in which R is as initially defined and Hal represents a chlorine, bromine or iodine atom, or its acid addition salts, in a melt or in a solvent, and a compound obtained from the general formula I is transformed in case then desired in its salt with a physiologically compatible organic or inorganic acid. (Machine-translation by Google Translate, not legally binding)
ES411407A 1973-02-08 1973-02-08 Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding) Expired ES411407A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES411407A ES411407A1 (en) 1973-02-08 1973-02-08 Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES411407A ES411407A1 (en) 1973-02-08 1973-02-08 Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding)

Publications (1)

Publication Number Publication Date
ES411407A1 true ES411407A1 (en) 1976-01-01

Family

ID=8463333

Family Applications (1)

Application Number Title Priority Date Filing Date
ES411407A Expired ES411407A1 (en) 1973-02-08 1973-02-08 Procedure for the preparation of new oxazoles. (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES411407A1 (en)

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19860315