ES359298A2 - Procedure for the production of new 3-aminosidnoni- mines replaced. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for the production of new 3-aminosidnoni- mines replaced. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES359298A2 ES359298A2 ES359298A ES359298A ES359298A2 ES 359298 A2 ES359298 A2 ES 359298A2 ES 359298 A ES359298 A ES 359298A ES 359298 A ES359298 A ES 359298A ES 359298 A2 ES359298 A2 ES 359298A2
- Authority
- ES
- Spain
- Prior art keywords
- substituted
- alcohol
- optionally
- group
- aryl
- 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
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- -1 cycloalcoyl Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 2
- 101100134922 Gallus gallus COR5 gene Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- BQIKRTGTPBOIMK-UHFFFAOYSA-N [O]C[O] Chemical compound [O]C[O] BQIKRTGTPBOIMK-UHFFFAOYSA-N 0.000 abstract 1
- 125000003158 alcohol group Chemical group 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- SRANPMHVZAXTBA-UHFFFAOYSA-N n-(cyanomethyl)nitrous amide Chemical class O=NNCC#N SRANPMHVZAXTBA-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Tires In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Improvements introduced in the object of the main patent No. 343,818 applied for on 4.10.67 by "Procedure for the production of new substituted 3-amino-sidnonimines" of the general formula **(See formula)** wherein R1 and R2, which may be the same or different, signify alcoholic, alkenyl, alkynyl, cycloalcoyl, aryl, or aralkoxy groups which may be additionally substituted by halogen atoms, CN-, -CF3- radicals, alcohol, dialkoxylamino, dialkoxylaminoalcoyl, hydroxy, alkoxy, acyloxy, acyl, or hydroxyalkoxy, or an oxydimethylene radical or a methylenedioxy radical, or a heterocyclic ring attached to the nitrogen atom of the 3-amino group via an alcohol chain, or together with the nitrogen atom can form a system of heterocyclic ring, which may optionally contain other heteroatoms and may optionally be substituted by one or more halogen atoms, hydroxy groups or lower alcohol radicals, alkoxy, acyl, acyloxy, hydroxyalkoxy, alkoxyalcoyl or halogenoalcoyl or an aryl or aralcoyl group, R3 means hydrogen, an alcohol or aralcohyl group, R4 means hydrogen or the COR5 group, R5 means an alcohol or alkoxy radical or a ra optionally substituted aryl, aralcoyl, cycloalcoyl or heterocyclic dical, and X means the remainder of a strong acid, by reaction of a substituted N-nitroso-amino-acetonitrile of the general formula **(See formula)** in which R1, R2 and R3 have the aforementioned meanings, with a cycle-closing agent to form the corresponding substituted sidnonimine, characterized in that a compound of the general formula is reacted with an appropriate nitrosating agent **(See formula)** where R1, R2, and R3 have the aforementioned meanings, OR6 means the rest of an alcohol and X means a halogen atom, and the nitrosated compound thus obtained is transformed, preferably without prior isolation, with a cycle-closing agent in the correspondingly substituted sidnonimine, it is converted, if desired, in a manner known per se, into an acid addition salt, and optionally acylated at the nitrogen atom 6. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19671670281 DE1670281A1 (en) | 1967-10-23 | 1967-10-23 | Process for the preparation of new substituted 3-amino-sydnonimines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES359298A2 true ES359298A2 (en) | 1970-06-01 |
Family
ID=5686303
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES359298A Expired ES359298A2 (en) | 1967-10-23 | 1968-10-18 | Procedure for the production of new 3-aminosidnoni- mines replaced. (Machine-translation by Google Translate, not legally binding) |
Country Status (5)
| Country | Link |
|---|---|
| AT (1) | AT287710B (en) |
| DK (1) | DK123103B (en) |
| ES (1) | ES359298A2 (en) |
| FI (1) | FI49412C (en) |
| SE (1) | SE343065B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3819914A1 (en) * | 1988-06-11 | 1989-12-21 | Cassella Ag | SUBSTITUTED 3-AMINO-DYNONOMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE |
-
1968
- 1968-10-14 FI FI682902A patent/FI49412C/en active
- 1968-10-18 ES ES359298A patent/ES359298A2/en not_active Expired
- 1968-10-22 SE SE14256/68A patent/SE343065B/xx unknown
- 1968-10-22 DK DK508568AA patent/DK123103B/en not_active IP Right Cessation
- 1968-10-23 AT AT1034868A patent/AT287710B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FI49412C (en) | 1975-06-10 |
| SE343065B (en) | 1972-02-28 |
| FI49412B (en) | 1975-02-28 |
| DK123103B (en) | 1972-05-15 |
| AT287710B (en) | 1971-02-10 |
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