GB1201212A - Tricyclic acids, process for their manufacture and compositions containing them - Google Patents
Tricyclic acids, process for their manufacture and compositions containing themInfo
- Publication number
- GB1201212A GB1201212A GB4432/68A GB443268A GB1201212A GB 1201212 A GB1201212 A GB 1201212A GB 4432/68 A GB4432/68 A GB 4432/68A GB 443268 A GB443268 A GB 443268A GB 1201212 A GB1201212 A GB 1201212A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- methoxy
- resulting
- hydroxy
- prepared
- 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
- 239000002253 acid Substances 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 150000007513 acids Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 12
- -1 alkenylene radical Chemical class 0.000 abstract 8
- 238000006243 chemical reaction Methods 0.000 abstract 8
- 150000002148 esters Chemical class 0.000 abstract 5
- 150000002825 nitriles Chemical class 0.000 abstract 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 230000007062 hydrolysis Effects 0.000 abstract 4
- 238000006460 hydrolysis reaction Methods 0.000 abstract 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- QOWAWWLGBCNRSP-UHFFFAOYSA-N 6-hydroxy-2-phenyl-3,4-dihydro-2h-naphthalen-1-one Chemical class C1CC2=CC(O)=CC=C2C(=O)C1C1=CC=CC=C1 QOWAWWLGBCNRSP-UHFFFAOYSA-N 0.000 abstract 2
- XSTDIWNKASNIET-UHFFFAOYSA-N 6-methoxy-2-phenyl-3,4-dihydro-2h-naphthalen-1-one Chemical compound C1CC2=CC(OC)=CC=C2C(=O)C1C1=CC=CC=C1 XSTDIWNKASNIET-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- IOLQWGVDEFWYNP-UHFFFAOYSA-N ethyl 2-bromo-2-methylpropanoate Chemical compound CCOC(=O)C(C)(C)Br IOLQWGVDEFWYNP-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- 150000002576 ketones Chemical class 0.000 abstract 2
- 229910052763 palladium Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 abstract 2
- 159000000000 sodium salts Chemical class 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 abstract 1
- NHDODQWIKUYWMW-UHFFFAOYSA-N 1-bromo-4-chlorobenzene Chemical compound ClC1=CC=C(Br)C=C1 NHDODQWIKUYWMW-UHFFFAOYSA-N 0.000 abstract 1
- XVNAQBXAGBAWEE-UHFFFAOYSA-N 4-(3-methoxyphenyl)butanoic acid Chemical compound COC1=CC=CC(CCCC(O)=O)=C1 XVNAQBXAGBAWEE-UHFFFAOYSA-N 0.000 abstract 1
- MGGLDVOWUYONER-UHFFFAOYSA-N 4-(3-methoxyphenyl)butanoyl chloride Chemical compound COC1=CC=CC(CCCC(Cl)=O)=C1 MGGLDVOWUYONER-UHFFFAOYSA-N 0.000 abstract 1
- RZVCIXULBVVOOW-UHFFFAOYSA-N 5-(4-chlorophenyl)-5,6,7,8-tetrahydronaphthalen-1-ol Chemical compound ClC1=CC=C(C=C1)C1CCCC2=C(C=CC=C12)O RZVCIXULBVVOOW-UHFFFAOYSA-N 0.000 abstract 1
- YPPZCRZRQHFRBH-UHFFFAOYSA-N 5-hydroxy-3,4-dihydro-2h-naphthalen-1-one Chemical class O=C1CCCC2=C1C=CC=C2O YPPZCRZRQHFRBH-UHFFFAOYSA-N 0.000 abstract 1
- BRCPWISABURVIH-UHFFFAOYSA-N 5-methoxy-3,4-dihydro-2h-naphthalen-1-one Chemical compound O=C1CCCC2=C1C=CC=C2OC BRCPWISABURVIH-UHFFFAOYSA-N 0.000 abstract 1
- GRCIEQRKSUAZRI-UHFFFAOYSA-N 5-phenyl-5,6,7,8-tetrahydronaphthalen-2-ol Chemical compound C1CCC2=CC(O)=CC=C2C1C1=CC=CC=C1 GRCIEQRKSUAZRI-UHFFFAOYSA-N 0.000 abstract 1
- FNSQPQKPPGALFA-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-2h-naphthalen-1-one Chemical class O=C1CCCC2=CC(O)=CC=C21 FNSQPQKPPGALFA-UHFFFAOYSA-N 0.000 abstract 1
- ZFOMLKXVQFNZPD-UHFFFAOYSA-N 6-methoxy-1-phenyl-1,2,3,4-tetrahydronaphthalene Chemical compound C1CCC2=CC(OC)=CC=C2C1C1=CC=CC=C1 ZFOMLKXVQFNZPD-UHFFFAOYSA-N 0.000 abstract 1
- BMIKETYHMQSVGT-UHFFFAOYSA-N 6-methoxy-1-phenyl-3,4-dihydro-2H-naphthalen-1-ol Chemical compound C1(=CC=CC=C1)C1(CCCC2=CC(=CC=C12)OC)O BMIKETYHMQSVGT-UHFFFAOYSA-N 0.000 abstract 1
- HFBFEWBKKXQBQN-UHFFFAOYSA-N 6-methoxy-2-phenyl-1,2,3,4-tetrahydronaphthalene Chemical compound C1CC2=CC(OC)=CC=C2CC1C1=CC=CC=C1 HFBFEWBKKXQBQN-UHFFFAOYSA-N 0.000 abstract 1
- MNALUTYMBUBKNX-UHFFFAOYSA-N 6-methoxy-3,4-dihydro-2h-naphthalen-1-one Chemical compound O=C1CCCC2=CC(OC)=CC=C21 MNALUTYMBUBKNX-UHFFFAOYSA-N 0.000 abstract 1
- UTVSNCZURCQGEV-UHFFFAOYSA-N 6-phenyl-5,6,7,8-tetrahydronaphthalen-2-ol Chemical compound C1CC2=CC(O)=CC=C2CC1C1=CC=CC=C1 UTVSNCZURCQGEV-UHFFFAOYSA-N 0.000 abstract 1
- QYQXAFMTCAPURI-UHFFFAOYSA-N 7-methoxy-3-phenyl-1,2-dihydronaphthalene Chemical compound C1CC2=CC(OC)=CC=C2C=C1C1=CC=CC=C1 QYQXAFMTCAPURI-UHFFFAOYSA-N 0.000 abstract 1
- LGLVJTQUMANFJQ-UHFFFAOYSA-N 7-methoxy-4-phenyl-1,2-dihydronaphthalene Chemical compound C=1CCC2=CC(OC)=CC=C2C=1C1=CC=CC=C1 LGLVJTQUMANFJQ-UHFFFAOYSA-N 0.000 abstract 1
- VKALOSVOLYOVDN-UHFFFAOYSA-N 8-phenyl-5,6,7,8-tetrahydronaphthalen-2-ol Chemical class OC1=CC=C2CCCC(C2=C1)C1=CC=CC=C1 VKALOSVOLYOVDN-UHFFFAOYSA-N 0.000 abstract 1
- 239000007818 Grignard reagent Substances 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- SXXLODUDAOBEFV-UHFFFAOYSA-M [Cl-].[Cd+]c1ccccc1 Chemical compound [Cl-].[Cd+]c1ccccc1 SXXLODUDAOBEFV-UHFFFAOYSA-M 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- FFSAXUULYPJSKH-UHFFFAOYSA-N butyrophenone Chemical compound CCCC(=O)C1=CC=CC=C1 FFSAXUULYPJSKH-UHFFFAOYSA-N 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- FGIWPOAWXBTJCS-UHFFFAOYSA-N ethyl 2-methyl-2-[(5-oxo-6-phenyl-7,8-dihydro-6H-naphthalen-2-yl)oxy]propanoate Chemical compound O=C1C(CCC2=CC(=CC=C12)OC(C(=O)OCC)(C)C)C1=CC=CC=C1 FGIWPOAWXBTJCS-UHFFFAOYSA-N 0.000 abstract 1
- 230000000871 hypocholesterolemic effect Effects 0.000 abstract 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229910000033 sodium borohydride Inorganic materials 0.000 abstract 1
- 239000012279 sodium borohydride Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/72—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings and other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
- C07C37/055—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/367—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61234567A | 1967-01-30 | 1967-01-30 | |
| US67915367A | 1967-10-30 | 1967-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1201212A true GB1201212A (en) | 1970-08-05 |
Family
ID=27086745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4432/68A Expired GB1201212A (en) | 1967-01-30 | 1968-01-29 | Tricyclic acids, process for their manufacture and compositions containing them |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3515746A (OSRAM) |
| AT (5) | AT283334B (OSRAM) |
| BE (1) | BE710034A (OSRAM) |
| CH (1) | CH498070A (OSRAM) |
| DE (1) | DE1643860A1 (OSRAM) |
| FR (3) | FR1570489A (OSRAM) |
| GB (1) | GB1201212A (OSRAM) |
| NL (1) | NL6801290A (OSRAM) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3642869A (en) * | 1969-07-30 | 1972-02-15 | Squibb & Sons Inc | 5 8-dihydronaphthyloxy acetic acids |
| US7001926B2 (en) * | 2000-03-10 | 2006-02-21 | Oxigene, Inc. | Tubulin binding agents and corresponding prodrug constructs |
| CN108794308B (zh) * | 2017-04-27 | 2021-07-20 | 北京大学深圳研究生院 | 1,2,3,4-四氢萘类化合物及其制备方法和应用 |
| CN109956854B (zh) * | 2019-04-30 | 2022-01-14 | 湖南第一师范学院 | 一种7-甲氧基-3-苯基-1,2-二氢萘的制备方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3243441A (en) * | 1962-07-26 | 1966-03-29 | Cassella Farbwerke Mainkur Ag | 7-hydroxy coumarin derivative |
| US3347910A (en) * | 1964-12-10 | 1967-10-17 | Merck & Co Inc | Cycloaliphatic substituted naphthyloxy-alkanoic acids and a method for their preparation |
-
1967
- 1967-10-30 US US679153A patent/US3515746A/en not_active Expired - Lifetime
-
1968
- 1968-01-03 CH CH568A patent/CH498070A/de not_active IP Right Cessation
- 1968-01-23 DE DE19681643860 patent/DE1643860A1/de active Pending
- 1968-01-25 FR FR1570489D patent/FR1570489A/fr not_active Expired
- 1968-01-29 AT AT04941/69A patent/AT283334B/de not_active IP Right Cessation
- 1968-01-29 AT AT86468A patent/AT283328B/de not_active IP Right Cessation
- 1968-01-29 AT AT04933/69A patent/AT283332B/de not_active IP Right Cessation
- 1968-01-29 NL NL6801290A patent/NL6801290A/xx unknown
- 1968-01-29 AT AT493969A patent/AT283333B/de not_active IP Right Cessation
- 1968-01-29 BE BE710034D patent/BE710034A/xx unknown
- 1968-01-29 GB GB4432/68A patent/GB1201212A/en not_active Expired
- 1968-01-29 AT AT494069A patent/AT284096B/de not_active IP Right Cessation
- 1968-04-25 FR FR149446A patent/FR7489M/fr not_active Expired
- 1968-04-25 FR FR149447A patent/FR7490M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL6801290A (OSRAM) | 1968-07-31 |
| BE710034A (OSRAM) | 1968-07-29 |
| AT283328B (de) | 1970-08-10 |
| DE1643860A1 (de) | 1971-06-09 |
| FR7490M (OSRAM) | 1969-12-08 |
| CH498070A (de) | 1970-10-31 |
| FR1570489A (OSRAM) | 1969-06-13 |
| AT283333B (de) | 1970-08-10 |
| AT283334B (de) | 1970-08-10 |
| FR7489M (OSRAM) | 1969-12-08 |
| AT283332B (de) | 1970-08-10 |
| US3515746A (en) | 1970-06-02 |
| AT284096B (de) | 1970-08-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |