ES437257A1 - Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding)

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Publication number
ES437257A1
ES437257A1 ES0437257A ES437257A ES437257A1 ES 437257 A1 ES437257 A1 ES 437257A1 ES 0437257 A ES0437257 A ES 0437257A ES 437257 A ES437257 A ES 437257A ES 437257 A1 ES437257 A1 ES 437257A1
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ES
Spain
Prior art keywords
group
translation
procedure
formula
preparation
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
ES0437257A
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.)
Kali Chemie AG
Original Assignee
Kali Chemie 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 Kali Chemie AG filed Critical Kali Chemie AG
Priority to ES0437257A priority Critical patent/ES437257A1/en
Publication of ES437257A1 publication Critical patent/ES437257A1/en
Expired legal-status Critical Current

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Abstract

Procedure for the preparation of new 1.5 benzodiazocins of the general formula **(See formula)** wherein R1 represents hydrogen or a low molecular weight, optionally substituted, straight or branched alcohol, alkenyl, alkynyl or cycloalkoxy radical; R2 signifies a halogen atom, a hydroxy group or an acyloxy group, and phenyl radicals A and B are optionally substituted with one or more substituents, namely nitro, trifluoromethyl, halogen, alcohol, alkoxy or thiomethyl, or in which possibly two contiguous carbon atoms of the phenyl radicals are linked through an alcoholenedioxy group; as well as its acid addition salts, characterized in that an acyldiamine of the general formula is cyclized **(See formula)** in which R1, A and B have the aforementioned meanings and R means a hydroxy or acyloxy group, at elevated temperature, optionally in an inert solvent with phosphorous oxyhalides, preferably phosphorous oxychloride, if desired an acyloxy group is transformed into the hydroxy group and eventually the compounds of formula I obtained are transformed into their salts by the addition of acid. (Machine-translation by Google Translate, not legally binding)
ES0437257A 1975-04-30 1975-04-30 Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding) Expired ES437257A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES0437257A ES437257A1 (en) 1975-04-30 1975-04-30 Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES0437257A ES437257A1 (en) 1975-04-30 1975-04-30 Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding)

Publications (1)

Publication Number Publication Date
ES437257A1 true ES437257A1 (en) 1977-01-16

Family

ID=59033309

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0437257A Expired ES437257A1 (en) 1975-04-30 1975-04-30 Procedure for the preparation of new 1,5-benzodiazocinas (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES437257A1 (en)

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