BE627999A - - Google Patents
Info
- Publication number
- BE627999A BE627999A BE627999DA BE627999A BE 627999 A BE627999 A BE 627999A BE 627999D A BE627999D A BE 627999DA BE 627999 A BE627999 A BE 627999A
- Authority
- BE
- Belgium
- Prior art keywords
- general formula
- preparation process
- formula
- process according
- signifies
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 10
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 235000019441 ethanol Nutrition 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 150000001340 alkali metals Chemical class 0.000 claims description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- YTRNSQPXEDGWMR-UHFFFAOYSA-N 2-cyclohexyl-2-hydroxy-2-phenylacetic acid Chemical compound C=1C=CC=CC=1C(O)(C(=O)O)C1CCCCC1 YTRNSQPXEDGWMR-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atoms Chemical group 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims 2
- 240000000489 Agave utahensis Species 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 159000000000 sodium salts Chemical class 0.000 claims 1
- 239000002253 acid Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-Dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 229940091292 Alo Drugs 0.000 description 1
- 210000003445 Biliary Tract Anatomy 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N N,N'-dimethylhydrazine Chemical class CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- 210000001635 Urinary Tract Anatomy 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000002567 autonomic Effects 0.000 description 1
- 239000000812 cholinergic antagonist Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001079 digestive Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drugs Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- -1 phenyl-cyclohexyl-hydroxy acetoxy Chemical group 0.000 description 1
- 239000001184 potassium carbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002048 spasmolytic Effects 0.000 description 1
- 230000001148 spastic Effects 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE627999A true BE627999A (de) |
Family
ID=198083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE627999D BE627999A (de) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE627999A (de) |
-
0
- BE BE627999D patent/BE627999A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4673686A (en) | New substituted heterocyclic benzamides, methods of preparing them and their application as behavior modifiers | |
| CA1097647A (fr) | Procede de preparation de nouvelles imidazoquinoleines et de leurs sels | |
| JPH038333B2 (de) | ||
| BE627999A (de) | ||
| CA1298301C (fr) | Benzamides, leur procede d'obtention et leurs applications therapeutiques | |
| FR2531709A1 (fr) | Diazabicyclooctanes, procede pour leur preparation et compositions pharmaceutiques les renfermant | |
| CH392483A (fr) | Procédé de préparation de nouveaux esters d'acides 4-halo-3-sulfamoyl-benzoïques | |
| Dox et al. | SPIRO-PYRIMIDINES. II. CYCLOHEXANE-1, 5-SPIRO-PYRIMIDINES. | |
| BE505352A (de) | ||
| BE503348A (de) | ||
| BE858978A (fr) | Nouveaux 2,3-dijydro imidazo (2,1-b) thiazoles, leur procede de preparation et leur application en therapeutique | |
| Jacobs et al. | THE QUATERNARY SALTS OF HEXAMETHYLENE-TETRAMINE. V. MONOHALOGENACETYL DERIVATIVES OF AMINOALCOHOLS AND THE HEXAMETHYLENETETRAMINIUM SALTS DERIVED THEREFROM, ¹ | |
| FR2547726A1 (fr) | Acide 2-(4-biphenylyl)-4-hexenoique et ses derives ayant une activite anti-inflammatoire | |
| FR2526021A1 (fr) | Procede de preparation de 3-hydroxy-benzodiazepinones | |
| BE634833A (de) | ||
| BE513130A (de) | ||
| CH412897A (fr) | Procédé de préparation d'amino oxazolinones | |
| CH626806A5 (en) | 2-Amino-3-(-5- and -6-)benzoylphenylacetic acid derivatives and process for preparing them | |
| BE504827A (de) | ||
| BE625134A (de) | ||
| BE630848A (de) | ||
| BE557023A (de) | ||
| CH534677A (fr) | Procédé de préparation d'acides bis-chromone-carboxyliques | |
| BE550677A (de) | ||
| BE620169A (de) |