GB919177A - Substituted ethylenediamines - Google Patents
Substituted ethylenediaminesInfo
- Publication number
- GB919177A GB919177A GB31643/60A GB3164360A GB919177A GB 919177 A GB919177 A GB 919177A GB 31643/60 A GB31643/60 A GB 31643/60A GB 3164360 A GB3164360 A GB 3164360A GB 919177 A GB919177 A GB 919177A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reacting
- carbon atoms
- ethylenediamine
- reactive ester
- appropriately substituted
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/02—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of compounds containing imino groups
Abstract
The invention comprises substituted ethylenediamines of the formula R1R2N.CHR3.CHR4.NR5R6 (wherein R1 is a tertiary alkyl radical, R2, R3, R4 and R5 are hydrogen atoms or alkyl radicals of at most 4 carbon atoms, and R6 is an alkyl or alkenyl radical of at most 10 carbon atoms) but excludes N,N1-di-(t-butyl)-ethylenediamine; and their acid-addition salts; and their preparation by (1) reacting a reactive ester of an appropriately substituted amino-alcohol with an appropriately substituted amine; or (2) alkylating with a reactive ester of a C1-4 alkanol an appropriately substituted ethylenediamine containing at least one hydrogen atom on a nitrogen atom; or (3) reductively alkylating with an aliphatic aldehyde containing at most 4 carbon atoms and a reducing agent an ethylene diamine as specified under (2); or (4) reacting a reactive ester of an appropriate dihydroxyalkane with an appropriate primary or secondary amine, to give a symmetrically substituted ethylenediamine. Detailed examples are given, and a list of suitable salt-forming inorganic and organic acids is provided. 2-Tertiary-butylaminoethyl chloride hydrochloride is prepared by reacting t-butylamine with ethylenechlorohydrin to give 2-t-butylaminoethanol, converting this to the hydrochloride and reacting this with thionyl chloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31643/60A GB919177A (en) | 1960-09-14 | 1960-09-14 | Substituted ethylenediamines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31643/60A GB919177A (en) | 1960-09-14 | 1960-09-14 | Substituted ethylenediamines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB919177A true GB919177A (en) | 1963-02-20 |
Family
ID=10326238
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31643/60A Expired GB919177A (en) | 1960-09-14 | 1960-09-14 | Substituted ethylenediamines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB919177A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997001360A2 (en) * | 1995-06-26 | 1997-01-16 | Concat, Ltd. | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
EP1513825A2 (en) * | 2002-05-17 | 2005-03-16 | Department of Health and Human Services | Anti tubercular drug: compositions and methods |
US8198303B2 (en) | 2002-05-17 | 2012-06-12 | Sequella, Inc. | Methods of use and compositions for the diagnosis and treatment of infectious diseases |
-
1960
- 1960-09-14 GB GB31643/60A patent/GB919177A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997001360A2 (en) * | 1995-06-26 | 1997-01-16 | Concat, Ltd. | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
WO1997001360A3 (en) * | 1995-06-26 | 1997-03-13 | Concat Ltd | Compounds with chelation affinity and selectivity for first transition series elements and their use in medical therapy and diagnosis |
US5874573A (en) * | 1995-06-26 | 1999-02-23 | Concat, Inc. | Compounds with chelation affinity and selectivity for first transition series elements: use in medical therapy |
AU703340B2 (en) * | 1995-06-26 | 1999-03-25 | Chelator Llc | Compounds with chelation affinity and selectivity for first transition series elements, and their use in medical therapy and diagnosis |
US6583182B1 (en) | 1995-06-26 | 2003-06-24 | Chelator Llc | Compounds with chelation affinity and selectivity for first transition series elements: use in medical therapy and diagnosis |
EP1513825A2 (en) * | 2002-05-17 | 2005-03-16 | Department of Health and Human Services | Anti tubercular drug: compositions and methods |
EP1513825A4 (en) * | 2002-05-17 | 2011-01-05 | Dept of Health and Human Services | Anti tubercular drug: compositions and methods |
US8198303B2 (en) | 2002-05-17 | 2012-06-12 | Sequella, Inc. | Methods of use and compositions for the diagnosis and treatment of infectious diseases |
US8268894B2 (en) | 2002-05-17 | 2012-09-18 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Compositions and methods for the treatment of infectious diseases |
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