GB1477997A - Phenylalkanols and their preparation - Google Patents
Phenylalkanols and their preparationInfo
- Publication number
- GB1477997A GB1477997A GB1780576A GB1780576A GB1477997A GB 1477997 A GB1477997 A GB 1477997A GB 1780576 A GB1780576 A GB 1780576A GB 1780576 A GB1780576 A GB 1780576A GB 1477997 A GB1477997 A GB 1477997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reacting
- substituted
- compound
- prepared
- biphenylyl
- 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 methyl magnesium halide Chemical class 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (1R)-1,3-butanediol Natural products CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 1
- JEQDSBVHLKBEIZ-REOHCLBHSA-N (2s)-2-chloropropanoyl chloride Chemical compound C[C@H](Cl)C(Cl)=O JEQDSBVHLKBEIZ-REOHCLBHSA-N 0.000 abstract 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 abstract 1
- RUYZJEIKQYLEGZ-UHFFFAOYSA-N 1-fluoro-4-phenylbenzene Chemical group C1=CC(F)=CC=C1C1=CC=CC=C1 RUYZJEIKQYLEGZ-UHFFFAOYSA-N 0.000 abstract 1
- CWYRBOMWOQXYFZ-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-phenylethanone Chemical compound C1=CC(F)=CC=C1CC(=O)C1=CC=CC=C1 CWYRBOMWOQXYFZ-UHFFFAOYSA-N 0.000 abstract 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004358 Butane-1, 3-diol Substances 0.000 abstract 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 abstract 1
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 150000008062 acetophenones Chemical class 0.000 abstract 1
- 230000002776 aggregation Effects 0.000 abstract 1
- 238000004220 aggregation Methods 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 abstract 1
- 210000001772 blood platelet Anatomy 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 235000019437 butane-1,3-diol Nutrition 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 235000012000 cholesterol Nutrition 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000012954 diazonium Substances 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 abstract 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000001939 inductive effect Effects 0.000 abstract 1
- 229910001506 inorganic fluoride Inorganic materials 0.000 abstract 1
- 229910001502 inorganic halide Inorganic materials 0.000 abstract 1
- XBEREOHJDYAKDA-UHFFFAOYSA-N lithium;propane Chemical compound [Li+].CC[CH2-] XBEREOHJDYAKDA-UHFFFAOYSA-N 0.000 abstract 1
- 210000004185 liver Anatomy 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 238000006396 nitration reaction Methods 0.000 abstract 1
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- OMSUIQOIVADKIM-UHFFFAOYSA-N rac-3-Hydroxybutyric acid ethyl ester Natural products CCOC(=O)CC(C)O OMSUIQOIVADKIM-UHFFFAOYSA-N 0.000 abstract 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 abstract 1
- 229940116269 uric acid Drugs 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/295—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing hydroxy or O-metal groups
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 |
|---|---|---|---|
| DE19752519719 DE2519719A1 (de) | 1975-05-02 | 1975-05-02 | Phenylalkanole und verfahren zu ihrer herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1477997A true GB1477997A (en) | 1977-06-29 |
Family
ID=5945662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1780576A Expired GB1477997A (en) | 1975-05-02 | 1976-04-30 | Phenylalkanols and their preparation |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4060633A (enExample) |
| JP (1) | JPS51138637A (enExample) |
| AT (1) | AT348510B (enExample) |
| AU (1) | AU499362B2 (enExample) |
| BE (1) | BE841329A (enExample) |
| CA (1) | CA1077962A (enExample) |
| CS (1) | CS200492B2 (enExample) |
| DD (1) | DD124593A5 (enExample) |
| DE (1) | DE2519719A1 (enExample) |
| DK (1) | DK156176A (enExample) |
| ES (1) | ES447365A1 (enExample) |
| FR (1) | FR2309217A1 (enExample) |
| GB (1) | GB1477997A (enExample) |
| HU (1) | HU176685B (enExample) |
| IE (1) | IE44100B1 (enExample) |
| IL (1) | IL49504A (enExample) |
| LU (1) | LU74869A1 (enExample) |
| NL (1) | NL7604623A (enExample) |
| SE (1) | SE7604954L (enExample) |
| ZA (1) | ZA762605B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2626018A1 (de) * | 1976-06-10 | 1977-12-22 | Merck Patent Gmbh | Alkinole und verfahren zu ihrer herstellung |
| US5380755A (en) * | 1992-07-24 | 1995-01-10 | The Du Pont Merck Pharmaceutical Company | Alkyl and alkylbenzyl ethers of substituted hydroquinones |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1040735A (en) * | 1964-07-23 | 1966-09-01 | British Drug Houses Ltd | 4-aryl-3-hydroxybutyric acid and esters, amides and salts thereof |
-
1975
- 1975-05-02 DE DE19752519719 patent/DE2519719A1/de not_active Withdrawn
-
1976
- 1976-03-31 DK DK156176A patent/DK156176A/da not_active IP Right Cessation
- 1976-04-21 FR FR7611675A patent/FR2309217A1/fr active Granted
- 1976-04-27 ES ES447365A patent/ES447365A1/es not_active Expired
- 1976-04-28 US US05/681,175 patent/US4060633A/en not_active Expired - Lifetime
- 1976-04-29 SE SE7604954A patent/SE7604954L/xx unknown
- 1976-04-29 NL NL7604623A patent/NL7604623A/xx not_active Application Discontinuation
- 1976-04-29 AT AT314876A patent/AT348510B/de not_active IP Right Cessation
- 1976-04-29 CS CS762831A patent/CS200492B2/cs unknown
- 1976-04-30 DD DD192623A patent/DD124593A5/xx unknown
- 1976-04-30 CA CA251,509A patent/CA1077962A/en not_active Expired
- 1976-04-30 GB GB1780576A patent/GB1477997A/en not_active Expired
- 1976-04-30 IE IE927/76A patent/IE44100B1/en unknown
- 1976-04-30 BE BE166609A patent/BE841329A/xx unknown
- 1976-04-30 ZA ZA762605A patent/ZA762605B/xx unknown
- 1976-04-30 AU AU13508/76A patent/AU499362B2/en not_active Expired
- 1976-04-30 IL IL49504A patent/IL49504A/xx unknown
- 1976-04-30 HU HU76ME1971A patent/HU176685B/hu unknown
- 1976-04-30 LU LU74869A patent/LU74869A1/xx unknown
- 1976-05-04 JP JP51051227A patent/JPS51138637A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CS200492B2 (en) | 1980-09-15 |
| IE44100B1 (en) | 1981-08-12 |
| FR2309217B1 (enExample) | 1979-09-21 |
| US4060633A (en) | 1977-11-29 |
| IL49504A (en) | 1979-01-31 |
| DD124593A5 (enExample) | 1977-03-02 |
| BE841329A (nl) | 1976-11-03 |
| NL7604623A (nl) | 1976-11-04 |
| CA1077962A (en) | 1980-05-20 |
| FR2309217A1 (fr) | 1976-11-26 |
| ZA762605B (en) | 1977-04-27 |
| DK156176A (da) | 1976-11-03 |
| ATA314876A (de) | 1978-07-15 |
| JPS51138637A (en) | 1976-11-30 |
| AU499362B2 (en) | 1979-04-12 |
| AU1350876A (en) | 1977-11-03 |
| LU74869A1 (enExample) | 1977-12-02 |
| DE2519719A1 (de) | 1976-11-18 |
| IE44100L (en) | 1976-11-02 |
| IL49504A0 (en) | 1976-06-30 |
| AT348510B (de) | 1979-02-26 |
| HU176685B (en) | 1981-04-28 |
| ES447365A1 (es) | 1977-12-01 |
| SE7604954L (sv) | 1976-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |