ES263315A1 - Procedure for the obtaining of new secondary amines (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for the obtaining of new secondary amines (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES263315A1 ES263315A1 ES0263315A ES263315A ES263315A1 ES 263315 A1 ES263315 A1 ES 263315A1 ES 0263315 A ES0263315 A ES 0263315A ES 263315 A ES263315 A ES 263315A ES 263315 A1 ES263315 A1 ES 263315A1
- Authority
- ES
- Spain
- Prior art keywords
- residue
- low
- translation
- machine
- legally binding
- 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
- 150000003335 secondary amines Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000000932 sedative agent Substances 0.000 abstract 1
- 230000001624 sedative effect Effects 0.000 abstract 1
- 230000000948 sympatholitic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/06—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Obtaining secondary amines of the formula **FORMULA** where R means a low hydrocarbon residue, which in the carbon chain may also be interrupted by oxygen, and R1 a low hydrocarbon residue, and its salts. The low hydrocarbon residue R, optionally interrupted by oxygen, is first of all aliphatic in nature, for example a low oxaalkyl residue, such as the 4-oxa-pentyl- (1) residue, or preferably a straight, low alkyl residue or branched, for example methyl, ethyl, allyl, isopropyl, butyl, butyl sec., amyl, isoamyl or hexyl, first and foremost, however, n-propyl. As low hydrocarbon residues R1 are mentioned the finishes indicated, before all alkyl residues, such as methyl. The new compounds and their salts have an outstanding sympatholytic effect with a component of sedative and bradycardial efficacy. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH8199559A CH390943A (en) | 1959-12-18 | 1959-12-18 | Process for the preparation of new secondary amines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES263315A1 true ES263315A1 (en) | 1961-03-01 |
Family
ID=4539322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0263315A Expired ES263315A1 (en) | 1959-12-18 | 1960-12-17 | Procedure for the obtaining of new secondary amines (Machine-translation by Google Translate, not legally binding) |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH390943A (en) |
| ES (1) | ES263315A1 (en) |
| FR (1) | FR1298929A (en) |
-
1959
- 1959-12-18 CH CH8199559A patent/CH390943A/en unknown
-
1960
- 1960-12-15 FR FR846960A patent/FR1298929A/en not_active Expired
- 1960-12-17 ES ES0263315A patent/ES263315A1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1298929A (en) | 1962-07-20 |
| CH390943A (en) | 1965-04-30 |
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