ES251786A1 - Procedimiento para la obtencion de nuevas amidas secundarias - Google Patents
Procedimiento para la obtencion de nuevas amidas secundariasInfo
- Publication number
- ES251786A1 ES251786A1 ES0251786A ES251786A ES251786A1 ES 251786 A1 ES251786 A1 ES 251786A1 ES 0251786 A ES0251786 A ES 0251786A ES 251786 A ES251786 A ES 251786A ES 251786 A1 ES251786 A1 ES 251786A1
- Authority
- ES
- Spain
- Prior art keywords
- ethyl
- amyl
- butyl
- methyl
- carbon atoms
- 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
- ZCDOIDIVOSTLIG-UHFFFAOYSA-N n-[2-(2-methoxyphenoxy)ethyl]propan-1-amine Chemical compound CCCNCCOC1=CC=CC=C1OC ZCDOIDIVOSTLIG-UHFFFAOYSA-N 0.000 title 1
- -1 aliphatic hydrocarbon radical Chemical class 0.000 abstract 8
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 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 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 2
- JJFOBACUIRKUPN-UHFFFAOYSA-N 2-bromoethoxybenzene Chemical class BrCCOC1=CC=CC=C1 JJFOBACUIRKUPN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 abstract 2
- 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 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- OMONCKYJLBVWOQ-UHFFFAOYSA-N 1-ethoxy-2-methoxybenzene Chemical compound CCOC1=CC=CC=C1OC OMONCKYJLBVWOQ-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000219 Sympatholytic Substances 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000000059 bradycardiac effect Effects 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000008298 dragée Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 229960001867 guaiacol Drugs 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- PGEYIIVEVARHEZ-UHFFFAOYSA-N n-benzyl-2-[2-(benzylamino)ethoxy]ethanamine Chemical group C=1C=CC=CC=1CNCCOCCNCC1=CC=CC=C1 PGEYIIVEVARHEZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 230000000948 sympatholitic effect Effects 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B11/00—Preservation of milk or dairy products
- A23B11/10—Preservation of milk or milk preparations
- A23B11/12—Preservation of milk or milk preparations by heating
- A23B11/13—Preservation of milk or milk preparations by heating the materials being loose unpacked
- A23B11/133—Preservation of milk or milk preparations by heating the materials being loose unpacked and progressively transported through the apparatus
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Chemical & Material Sciences (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH6459158A CH371458A (de) | 1958-10-02 | 1958-10-02 | Verfahren zur Herstellung neuer sekundärer Amine |
| CH7094359 | 1959-03-18 | ||
| CH7660059A CH383998A (de) | 1959-08-05 | 1959-08-05 | Verfahren zur Herstellung neuer sekundärer Amine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES251786A1 true ES251786A1 (es) | 1960-06-01 |
Family
ID=1859932
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0251786A Expired ES251786A1 (es) | 1958-10-02 | 1959-08-31 | Procedimiento para la obtencion de nuevas amidas secundarias |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3175006A (d) |
| BE (1) | BE583205A (d) |
| ES (1) | ES251786A1 (d) |
| FR (1) | FR1280575A (d) |
| GB (1) | GB879342A (d) |
| NL (1) | NL243932A (d) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1128052A (en) * | 1965-06-08 | 1968-09-25 | Ici Ltd | Alkanolamine derivatives |
| US4059622A (en) * | 1970-05-27 | 1977-11-22 | Imperial Chemical Industries Limited | Alkanolamine derivatives |
| SE399419B (sv) * | 1974-12-20 | 1978-02-13 | Astra Laekemedel Ab | Analogiforfarande for framstellning av nya lokalanestetiska foreningar |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2967201A (en) * | 1958-06-02 | 1961-01-03 | Lilly Co Eli | Alkylaminoalkyl ethers of phenols |
-
0
- NL NL243932A patent/NL243932A/xx unknown
- BE BE583205D patent/BE583205A/fr unknown
-
1959
- 1959-08-31 ES ES0251786A patent/ES251786A1/es not_active Expired
- 1959-09-17 GB GB31780/59A patent/GB879342A/en not_active Expired
- 1959-09-25 FR FR805989A patent/FR1280575A/fr not_active Expired
-
1963
- 1963-12-19 US US331965A patent/US3175006A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB879342A (en) | 1961-10-11 |
| FR1280575A (fr) | 1962-01-08 |
| US3175006A (en) | 1965-03-23 |
| BE583205A (d) | |
| NL243932A (d) | 1964-01-27 |
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