NO743116L - - Google Patents
Info
- Publication number
- NO743116L NO743116L NO743116A NO743116A NO743116L NO 743116 L NO743116 L NO 743116L NO 743116 A NO743116 A NO 743116A NO 743116 A NO743116 A NO 743116A NO 743116 L NO743116 L NO 743116L
- Authority
- NO
- Norway
- Prior art keywords
- general formula
- isopropylamino
- acetaminophenoxy
- naphthoxy
- hydroxy
- Prior art date
Links
- -1 aromatic 3-substituted 1-isopropylamino-2-propanols Chemical class 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000002894 organic compounds Chemical class 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000003756 stirring Methods 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229960004592 isopropanol Drugs 0.000 description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 4
- 229940092714 benzenesulfonic acid Drugs 0.000 description 4
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- DURULFYMVIFBIR-UHFFFAOYSA-N practolol Chemical compound CC(C)NCC(O)COC1=CC=C(NC(C)=O)C=C1 DURULFYMVIFBIR-UHFFFAOYSA-N 0.000 description 3
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- GRAOWBQCLZIQIW-UHFFFAOYSA-N n-[4-(2,3-dihydroxypropoxy)phenyl]acetamide Chemical compound CC(=O)NC1=CC=C(OCC(O)CO)C=C1 GRAOWBQCLZIQIW-UHFFFAOYSA-N 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol Chemical compound C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- BYNNMWGWFIGTIC-UHFFFAOYSA-N 3-naphthalen-1-yloxypropane-1,2-diol Chemical compound C1=CC=C2C(OCC(O)CO)=CC=CC2=C1 BYNNMWGWFIGTIC-UHFFFAOYSA-N 0.000 description 1
- 206010002383 Angina Pectoris Diseases 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000033764 rhythmic process Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C301/00—Esters of sulfurous acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI5474A FI48581C (fi) | 1974-01-09 | 1974-01-09 | Asetamino-fenoksi-propaanidiolin esterit, jotka ovat välituotteita val mistettaessa 1-isopropyyliamiini-3-(4-asetaminofenoksi)-2-propanolia. |
| FI5574A FI48582C (fi) | 1974-01-09 | 1974-01-09 | Naftoksi-propaanidiolin esterit, jotka ovat välituotteita valmistettae ssa 1-isopropyyliamino-3-naftoksi-2-propanolia. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO743116L true NO743116L (da) | 1975-08-04 |
Family
ID=26156268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO743116A NO743116L (da) | 1974-01-09 | 1974-08-30 |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPS50105626A (da) |
| CS (1) | CS175393B2 (da) |
| DK (1) | DK462174A (da) |
| NO (1) | NO743116L (da) |
| SE (1) | SE7409459L (da) |
-
1974
- 1974-07-19 SE SE7409459A patent/SE7409459L/xx unknown
- 1974-08-30 NO NO743116A patent/NO743116L/no unknown
- 1974-08-30 DK DK462174A patent/DK462174A/da unknown
- 1974-10-14 JP JP49118003A patent/JPS50105626A/ja active Pending
- 1974-11-27 CS CS8114A patent/CS175393B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE7409459L (da) | 1975-07-10 |
| JPS50105626A (da) | 1975-08-20 |
| CS175393B2 (da) | 1977-05-31 |
| DK462174A (da) | 1975-09-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU976847A3 (ru) | Способ получени производных 1-фенил-2,3,4,5-тетрагидро-1н-3-бензазепина или их солей | |
| NO764025L (da) | ||
| US4230873A (en) | Thiophene derivatives | |
| NO118394B (da) | ||
| PL106076B1 (pl) | Sposob wytwarzania nowych pochodnych tienotiazyny | |
| DK149230B (da) | Analogifremgangsmaade til fremstilling af 5-benzoyl-6-hydroxy-indan-1-carboxylsyrederivater eller farmaceutisk acceptable salte deraf | |
| NO128814B (da) | ||
| NO147809B (no) | Kraftturbin. | |
| NO743116L (da) | ||
| NO130549B (da) | ||
| NO152491B (no) | Kontinuerlig fremfoert spindelinnretning med bestemt lengdeforskjellstilling av fleksible roerformede gjenstander med ubestemt lengde | |
| CN105693632A (zh) | 一种多取代喹喔啉衍生物的制备方法 | |
| US4090020A (en) | Thienothiazine derivatives | |
| NO144039B (no) | Analogifremgangsmaate ved fremstilling av nye, terapeutisk virksomme benzofuranderivater | |
| CN107056700A (zh) | 一种四氢异喹啉类化合物外消旋体的半量拆分法 | |
| NO130329B (da) | ||
| FI62664C (fi) | Foerfarande foer framstaellning av nya terapeutiskt anvaendbara 6-piperazinyl-11-metylen-morfantridin-derivat | |
| US4175085A (en) | Thienothiazine derivatives | |
| US3136768A (en) | 8-(benzoyloxy)-quinolines | |
| KR860000591B1 (ko) | 피리딘 카복실산 유도체의 제조방법 | |
| NO154335B (no) | Fremgangsmate ved fjernelse av en vanadiumholding, vanding opplosning av en syre fra en dektivert avmettalliseringskatalysator | |
| NO159635B (no) | Hyllestativ med roerformede, i tverrsnitt polygonale hjoernesoeyler. | |
| NO753391L (da) | ||
| US2784194A (en) | Phenacylsulfonyl pyridine compounds | |
| US4134898A (en) | N-Carbalkoxymethylsulfamoyl thiophene carboxylic acid alkyl esters |