GB581230A - Manufacture of basic esters and amides of ª‡-substituted aryloxy acetic acids - Google Patents
Manufacture of basic esters and amides of ª‡-substituted aryloxy acetic acidsInfo
- Publication number
- GB581230A GB581230A GB16066/44A GB1606644A GB581230A GB 581230 A GB581230 A GB 581230A GB 16066/44 A GB16066/44 A GB 16066/44A GB 1606644 A GB1606644 A GB 1606644A GB 581230 A GB581230 A GB 581230A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ester
- acids
- acid
- reacted
- compounds
- 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
- -1 aryloxy acetic acids Chemical class 0.000 title abstract 15
- 150000002148 esters Chemical class 0.000 title abstract 7
- 235000011054 acetic acid Nutrition 0.000 title abstract 3
- 150000001408 amides Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- 150000007513 acids Chemical class 0.000 abstract 5
- 150000001414 amino alcohols Chemical class 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000005263 alkylenediamine group Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 150000003335 secondary amines Chemical class 0.000 abstract 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 abstract 1
- WTLYFCZMLRAPLI-UHFFFAOYSA-N 2-methoxyphenol;potassium Chemical compound [K].COC1=CC=CC=C1O WTLYFCZMLRAPLI-UHFFFAOYSA-N 0.000 abstract 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 150000001447 alkali salts Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000000812 cholinergic antagonist Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 229960002887 deanol Drugs 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- 235000019439 ethyl acetate Nutrition 0.000 abstract 1
- 229960003750 ethyl chloride Drugs 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000012433 hydrogen halide Substances 0.000 abstract 1
- 229910000039 hydrogen halide Inorganic materials 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 abstract 1
- 229940072033 potash Drugs 0.000 abstract 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 1
- 235000015320 potassium carbonate Nutrition 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 abstract 1
- 230000002048 spasmolytic effect Effects 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH581230X | 1943-07-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB581230A true GB581230A (en) | 1946-10-04 |
Family
ID=4521513
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB16066/44A Expired GB581230A (en) | 1943-07-30 | 1944-08-23 | Manufacture of basic esters and amides of ª‡-substituted aryloxy acetic acids |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE457027A (enrdf_load_stackoverflow) |
| GB (1) | GB581230A (enrdf_load_stackoverflow) |
| NL (1) | NL58836C (enrdf_load_stackoverflow) |
-
0
- NL NL58836D patent/NL58836C/xx active
-
1944
- 1944-07-29 BE BE457027A patent/BE457027A/fr unknown
- 1944-08-23 GB GB16066/44A patent/GB581230A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL58836C (enrdf_load_stackoverflow) | |
| BE457027A (enrdf_load_stackoverflow) | 1944-08-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB581230A (en) | Manufacture of basic esters and amides of ª‡-substituted aryloxy acetic acids | |
| US1810267A (en) | Alkyl-quinolyl-amino-phenyl carboxylic acids | |
| US3868418A (en) | Novel N-(ortho- and para-nitrobenzoyl)-sulfoximine intermediates and process for their production | |
| GB984471A (en) | Anthranilic acid esters and methods for producing the same | |
| GB815279A (en) | Novel benzomorpholone derivatives and a process for the manufacture thereof | |
| US2701254A (en) | Production of isochromanylacetic acids and their derivatives | |
| Benington et al. | The Chemistry of Hydrazyl free Radicals. II. Synthesis and Dissociation of Tetra (4-Fluorophenyl) Hydrazine | |
| ES8104805A1 (es) | Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas | |
| US2882287A (en) | Methylbutynyl stearate | |
| US2351409A (en) | Arylaminoketo compound and preparation | |
| McMillan et al. | Studies on the Willgerodt Reaction. V. An Anomalous Synthesis of Dithioöxalodimorpholide1 | |
| JPS557222A (en) | Preparation of aletheine derivative | |
| US3042712A (en) | Carboxylic acid amides | |
| US2063191A (en) | Hydroxy phenyl morpholines | |
| FI59989C (fi) | Foerfarande foer framstaellning av n-aminoalkyl-substituerade bensamider | |
| US3647813A (en) | Process for the manufacture of benzoxazolone-6-beta-hydroxy-ethyl-sulfone | |
| GB768840A (en) | Compounds containing a cyclopentyl ring | |
| US2336445A (en) | 4-substituted-2'-substituted diphenyl sulphone | |
| GB610198A (en) | The manufacture of ether-esters of organic hydroxy-acids | |
| JPS5576863A (en) | Preparation of 2-chloronicotinic acid | |
| GB782971A (en) | Basically substituted carboxylic acid amides and a process for making them | |
| GB728368A (en) | Improvements in or relating to the production of 3-pyrazolidones | |
| GB794239A (en) | Organic nitrogen compounds and process for producing the same | |
| GB667199A (en) | Process for stabilizing photographic emulsions | |
| GB820503A (en) | Improvements in or relating to the production of n-substituted 2-hydroxymethyl pyrrolidines |