ES259869A1 - Procedimiento para la obtenciën de un nuevo ester - Google Patents
Procedimiento para la obtenciën de un nuevo esterInfo
- Publication number
- ES259869A1 ES259869A1 ES0259869A ES259869A ES259869A1 ES 259869 A1 ES259869 A1 ES 259869A1 ES 0259869 A ES0259869 A ES 0259869A ES 259869 A ES259869 A ES 259869A ES 259869 A1 ES259869 A1 ES 259869A1
- Authority
- ES
- Spain
- Prior art keywords
- lower alkyl
- meal
- radical
- corn
- etherified
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 6
- 239000000543 intermediate Substances 0.000 title 1
- -1 ether radical Chemical class 0.000 abstract 13
- 150000003839 salts Chemical class 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 240000008042 Zea mays Species 0.000 abstract 7
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 7
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 7
- 235000005822 corn Nutrition 0.000 abstract 7
- 235000012054 meals Nutrition 0.000 abstract 6
- 150000001204 N-oxides Chemical class 0.000 abstract 5
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 235000019733 Fish meal Nutrition 0.000 abstract 2
- 108010068370 Glutens Proteins 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 abstract 2
- 235000019764 Soybean Meal Nutrition 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 239000004467 fishmeal Substances 0.000 abstract 2
- 235000021312 gluten Nutrition 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 235000010755 mineral Nutrition 0.000 abstract 2
- 238000002156 mixing Methods 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- JVHNBFFHWQQPLL-WOXROFTLSA-N reserpic acid Chemical class COC1=CC=C2C(CCN3C[C@H]4C[C@@H](O)[C@@H]([C@H]([C@H]4C[C@@H]33)C(O)=O)OC)=C3NC2=C1 JVHNBFFHWQQPLL-WOXROFTLSA-N 0.000 abstract 2
- 229960003147 reserpine Drugs 0.000 abstract 2
- 239000004455 soybean meal Substances 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- BZCOSCNPHJNQBP-UPHRSURJSA-N (z)-2,3-dihydroxybut-2-enedioic acid Chemical class OC(=O)C(\O)=C(\O)C(O)=O BZCOSCNPHJNQBP-UPHRSURJSA-N 0.000 abstract 1
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 abstract 1
- PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical class OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 abstract 1
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 abstract 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical class NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 abstract 1
- 125000005274 4-hydroxybenzoic acid group Chemical class 0.000 abstract 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical class CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 abstract 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 235000019743 Choline chloride Nutrition 0.000 abstract 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 abstract 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract 1
- 150000000994 L-ascorbates Chemical class 0.000 abstract 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 abstract 1
- 239000002841 Lewis acid Substances 0.000 abstract 1
- 240000004658 Medicago sativa Species 0.000 abstract 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract 1
- 229930003779 Vitamin B12 Natural products 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 abstract 1
- 150000005840 aryl radicals Chemical class 0.000 abstract 1
- 235000010323 ascorbic acid Nutrition 0.000 abstract 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 abstract 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 abstract 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 abstract 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 abstract 1
- 229960002079 calcium pantothenate Drugs 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 abstract 1
- 229960003178 choline chloride Drugs 0.000 abstract 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid Chemical class OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 abstract 1
- 150000001860 citric acid derivatives Chemical class 0.000 abstract 1
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000008049 diazo compounds Chemical class 0.000 abstract 1
- HBYOLNPZXLHVQA-UHFFFAOYSA-J dicalcium dicarbonate Chemical compound [Ca+2].[Ca+2].[O-]C([O-])=O.[O-]C([O-])=O HBYOLNPZXLHVQA-UHFFFAOYSA-J 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- DRSDCRSCGFTJCE-UHFFFAOYSA-N ethanol;4-methylbenzenesulfonic acid Chemical class CCO.CC1=CC=C(S(O)(=O)=O)C=C1 DRSDCRSCGFTJCE-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 235000019197 fats Nutrition 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000001077 hypotensive effect Effects 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([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
- 150000003903 lactic acid esters Chemical class 0.000 abstract 1
- 150000007517 lewis acids Chemical class 0.000 abstract 1
- 150000002688 maleic acid derivatives Chemical class 0.000 abstract 1
- 150000004701 malic acid derivatives Chemical class 0.000 abstract 1
- 150000002690 malonic acid derivatives Chemical class 0.000 abstract 1
- 239000011702 manganese sulphate Substances 0.000 abstract 1
- 235000007079 manganese sulphate Nutrition 0.000 abstract 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 abstract 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 1
- 229930182817 methionine Natural products 0.000 abstract 1
- 235000006109 methionine Nutrition 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 abstract 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 150000003901 oxalic acid esters Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 244000144977 poultry Species 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000004728 pyruvic acid derivatives Chemical class 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 235000019192 riboflavin Nutrition 0.000 abstract 1
- 239000002151 riboflavin Substances 0.000 abstract 1
- 229960002477 riboflavin Drugs 0.000 abstract 1
- 150000003902 salicylic acid esters Chemical class 0.000 abstract 1
- 235000002639 sodium chloride Nutrition 0.000 abstract 1
- 150000003900 succinic acid esters Chemical class 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 150000003899 tartaric acid esters Chemical class 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- 235000013343 vitamin Nutrition 0.000 abstract 1
- 239000011782 vitamin Substances 0.000 abstract 1
- 229940088594 vitamin Drugs 0.000 abstract 1
- 229930003231 vitamin Natural products 0.000 abstract 1
- 235000019155 vitamin A Nutrition 0.000 abstract 1
- 239000011719 vitamin A Substances 0.000 abstract 1
- 235000019163 vitamin B12 Nutrition 0.000 abstract 1
- 239000011715 vitamin B12 Substances 0.000 abstract 1
- 235000019166 vitamin D Nutrition 0.000 abstract 1
- 239000011710 vitamin D Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D459/00—Heterocyclic compounds containing benz [g] indolo [2, 3-a] quinolizine ring systems, e.g. yohimbine; 16, 18-lactones thereof, e.g. reserpic acid lactone
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/116—Heterocyclic compounds
- A23K20/137—Heterocyclic compounds containing two hetero atoms, of which at least one is nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Veterinary Medicine (AREA)
- Zoology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Husbandry (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83018759A | 1959-07-29 | 1959-07-29 | |
| US83735759A | 1959-09-01 | 1959-09-01 | |
| US37097A US3119819A (en) | 1959-07-29 | 1960-06-20 | Intermediates for 18-o-alkyl-reserpic acid esters and related compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES259869A1 true ES259869A1 (es) | 1961-03-16 |
Family
ID=27365147
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0259869A Expired ES259869A1 (es) | 1959-07-29 | 1960-07-26 | Procedimiento para la obtenciën de un nuevo ester |
| ES0259870A Expired ES259870A1 (es) | 1959-07-29 | 1960-07-26 | Procedimiento para la obtenciën de un nuevo ester |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0259870A Expired ES259870A1 (es) | 1959-07-29 | 1960-07-26 | Procedimiento para la obtenciën de un nuevo ester |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3119819A (OSRAM) |
| AT (1) | AT241693B (OSRAM) |
| CH (12) | CH414660A (OSRAM) |
| DE (1) | DE1197737B (OSRAM) |
| ES (2) | ES259869A1 (OSRAM) |
| FI (1) | FI40249B (OSRAM) |
| GB (1) | GB885981A (OSRAM) |
| SE (1) | SE314883B (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2102195T3 (es) * | 1992-12-28 | 1997-07-16 | Eisai Co Ltd | Derivados heterociclicos de acido carbonico que se fijan en receptores de retinoides. |
| CA2363067C (en) * | 1999-01-12 | 2012-03-20 | David J. Grainger | Compounds and methods to inhibit or augment an inflammatory response |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1045772B (de) * | 1956-04-24 | 1958-12-04 | Ciba Geigy | Wachstumsbeschleunigendes Beifuttermittel |
-
1960
- 1960-06-20 US US37097A patent/US3119819A/en not_active Expired - Lifetime
- 1960-07-14 CH CH1551064A patent/CH414660A/de unknown
- 1960-07-14 CH CH1551364A patent/CH388324A/de unknown
- 1960-07-14 CH CH1551164A patent/CH392539A/de unknown
- 1960-07-14 CH CH76465A patent/CH410971A/de unknown
- 1960-07-14 CH CH76265A patent/CH411917A/de unknown
- 1960-07-14 CH CH796860A patent/CH413850A/de unknown
- 1960-07-14 CH CH1551464A patent/CH388325A/de unknown
- 1960-07-14 CH CH1551264A patent/CH392540A/de unknown
- 1960-07-14 CH CH796560A patent/CH387054A/de unknown
- 1960-07-14 CH CH796760A patent/CH414656A/de unknown
- 1960-07-14 CH CH796660A patent/CH410967A/de unknown
- 1960-07-14 CH CH76365A patent/CH411918A/de unknown
- 1960-07-26 DE DEC25721A patent/DE1197737B/de active Pending
- 1960-07-26 ES ES0259869A patent/ES259869A1/es not_active Expired
- 1960-07-26 ES ES0259870A patent/ES259870A1/es not_active Expired
- 1960-07-28 AT AT579760A patent/AT241693B/de active
- 1960-07-29 GB GB26593/60A patent/GB885981A/en not_active Expired
-
1964
- 1964-04-13 SE SE454964A patent/SE314883B/xx unknown
- 1964-10-23 FI FI2236/64A patent/FI40249B/fi active
Also Published As
| Publication number | Publication date |
|---|---|
| CH414656A (de) | 1966-06-15 |
| CH387054A (de) | 1965-01-31 |
| CH414660A (de) | 1966-06-15 |
| CH411918A (de) | 1966-04-30 |
| AT241693B (de) | 1965-08-10 |
| SE314883B (OSRAM) | 1969-09-15 |
| CH410971A (de) | 1966-04-15 |
| CH410967A (de) | 1966-04-15 |
| DE1197737B (de) | 1965-07-29 |
| CH411917A (de) | 1966-04-30 |
| CH413850A (de) | 1966-05-31 |
| GB885981A (en) | 1962-01-03 |
| FI40249B (OSRAM) | 1968-07-31 |
| CH388325A (de) | 1965-02-28 |
| ES259870A1 (es) | 1961-03-16 |
| CH392539A (de) | 1965-05-31 |
| CH388324A (de) | 1965-02-28 |
| CH392540A (de) | 1965-05-31 |
| US3119819A (en) | 1964-01-28 |
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