ES343019A1 - Procedure for the obtaining of new phenyl-alcanolamines. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the obtaining of new phenyl-alcanolamines. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES343019A1
ES343019A1 ES343019A ES343019A ES343019A1 ES 343019 A1 ES343019 A1 ES 343019A1 ES 343019 A ES343019 A ES 343019A ES 343019 A ES343019 A ES 343019A ES 343019 A1 ES343019 A1 ES 343019A1
Authority
ES
Spain
Prior art keywords
group
compound
see formula
represents hydrogen
formula
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
ES343019A
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.)
CH Boehringer Sohn AG and Co KG
Original Assignee
CH Boehringer Sohn AG and Co KG
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 CH Boehringer Sohn AG and Co KG filed Critical CH Boehringer Sohn AG and Co KG
Publication of ES343019A1 publication Critical patent/ES343019A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A procedure for obtaining compounds of the general formula **(See formula)** in which R1 represents hydrogen or an acyl group, especially the radical of an aliphatic or aromatic carboxylic acid or an N-substituted carbamic acid, R2 represents a straight or branched lower alcohol group R3 is hydrogen or an alcohol group with 1 to 3 atoms Carbon and R4 is hydrogen, a straight or branched lower alcohol group, an acyl, formyl, carboalkoxy- or theophylline (7) -ethyl group, as well as its addition salts with physiologically tolerable acids characterized by reducing a) a compound of the general formula **(See formula)** in which R2, R3 and R4 have the indicated meanings and R represents the group R1 or a hydrogenolytic, hydrolytic or alcoholically separable protecting group, especially a benzyl or acyl group and R'represents hydrogen or, especially its R4 represents hydrogen or a group alcohol or a theophylline (7) -ethyl group, a protecting group, preferably a benzyl group, or reduce b) a compound of the general formula **(See formula)** in which R and R2 have the indicated meanings and Q represents the group (see formula), (in which R7 represents hydrogen or a straight or branched lower alcohol group) or the group (see formula) or reduce c) a compound of the general formula **(See formula)** in which R, R2 and R3 have the indicated meanings and R6 represents = C = O or = COHO groups, in the presence of a compound R5-NH2, in which R5 represents hydrogen, a straight or branched lower alcohol group or a group theophylline (7) -ethyl, or d) cleaving by the action of strong acids a compound of the general formula **(See formula)** in which R, R3 and R7 have the meanings indicated above or e) reacting a compound of the general formula **(See formula)** in which R2 has the meaning indicated above, E represents the group (see formula), or the group (see formula), (Y is a chlorine, bromine or iodine atom); and R'''represents a protecting group, preferably the benzyl group, with a compound of the general formula R5-NH-R'', in which R5 has the meaning indicated above and R''represents hydrogen or a benzyl group, and separating from the compounds obtained according to the working methods a) to e) possibly present protecting groups and optionally introducing into the compounds of formula I thus obtained, in which R1 represents hydrogen, an acyl group, and/or in which R4 represents hydrogen, a lower alcohol group, acyl, formyl, carboalkoxy or theophylline (7) -ethyl, and, optionally, converting the free bases obtained at the beginning into the acid addition salts and the salts obtained at the beginning into the free bases. (Machine-translation by Google Translate, not legally binding)
ES343019A 1966-07-18 1967-07-14 Procedure for the obtaining of new phenyl-alcanolamines. (Machine-translation by Google Translate, not legally binding) Expired ES343019A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB0088050 1966-07-18

Publications (1)

Publication Number Publication Date
ES343019A1 true ES343019A1 (en) 1968-08-16

Family

ID=6984091

Family Applications (1)

Application Number Title Priority Date Filing Date
ES343019A Expired ES343019A1 (en) 1966-07-18 1967-07-14 Procedure for the obtaining of new phenyl-alcanolamines. (Machine-translation by Google Translate, not legally binding)

Country Status (6)

Country Link
AT (3) AT287680B (en)
BE (1) BE701499A (en)
DE (1) DE1543359A1 (en)
ES (1) ES343019A1 (en)
FR (1) FR7177M (en)
NL (1) NL6709934A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2933005C2 (en) * 1979-08-14 1983-01-13 Klinge Pharma GmbH, 8000 München 1- (3-Acyloxyphenyl) -2-aminoethanols, their acid addition salts, medicaments containing them, and processes for their preparation

Also Published As

Publication number Publication date
BE701499A (en) 1968-01-18
NL6709934A (en) 1968-01-19
AT287677B (en) 1971-02-10
FR7177M (en) 1969-08-11
DE1543359A1 (en) 1972-04-13
AT287680B (en) 1971-02-10
AT287681B (en) 1971-02-10

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