ES421132A1 - Benzo-or naphtho-dipyran-di-n-tetrazolyl- -carboxamide derivative methods for their production and compositions containing them - Google Patents
Benzo-or naphtho-dipyran-di-n-tetrazolyl- -carboxamide derivative methods for their production and compositions containing themInfo
- Publication number
- ES421132A1 ES421132A1 ES421132A ES421132A ES421132A1 ES 421132 A1 ES421132 A1 ES 421132A1 ES 421132 A ES421132 A ES 421132A ES 421132 A ES421132 A ES 421132A ES 421132 A1 ES421132 A1 ES 421132A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- compound
- pairs
- chains
- benzene
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 33
- 150000001875 compounds Chemical class 0.000 abstract 12
- 150000002790 naphthalenes Chemical class 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 150000002431 hydrogen Chemical class 0.000 abstract 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- FMCAFXHLMUOIGG-JTJHWIPRSA-N (2s)-2-[[(2r)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-JTJHWIPRSA-N 0.000 abstract 1
- FMCAFXHLMUOIGG-IWFBPKFRSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-IWFBPKFRSA-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
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000005102 carbonylalkoxy group Chemical group 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
- 150000004820 halides Chemical class 0.000 abstract 1
- 238000007363 ring formation reaction Methods 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Procedure to produce a compound I, in which two chains of formula XX: **(See formula)** where each pair of R9 and R10 may be the same or different, and R9 and R10 are the same or different and are hydrogen, C1 to 6 alcohol, C2 to 6 alkenyl, phenyl, phenyl- (C1 to 6 alcohol), C2 to 6 alkanoyl or C2 to 6 carbonyl alkoxy, are respectively attached to two pairs of ortho positions of a benzene or naphthalene nucleus; or a pharmaceutically acceptable derivative thereof; comprising (a) producing a compound la in which two chains of formula XXa: **(See formula)** where R9 is as defined above, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus, removing an R11 group from a compound II in which two chains of formula, XXb: **(See formula)** where R9 is as defined above, and R11 represents a group that can be replaced by hydrogen, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus; (b) produce a compound Ib in which two chains of formula XXc: **(See formula)** where R10 is as defined above, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus, by (i) removing an R12 group from a compound VI in which two chains of formula XXd: **(See formula)** where R10 is as defined above and R12 represents a group that may be replaced by hydrogen, are attached to two pairs of ortho positions of a benzene or naphthalene nucleus, or (ii) cyclization of a compound VIII in which two chains of formula XXe: **(See formula)** where R10 is as defined above, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus; (c) produce a compound Ic in which two chains of formula XXy: **(See formula)** where R9y and R10y have the same meanings as the previous R9 and R10, except that it must be hydrogen when R10y is hydrogen, reacting a compound III in which two chains -COCH = C (COOH) -O- are linked to two pairs of ortho positions of a benzene or naphthalene nucleus, or an acid halide, an ester or a mixed anhydride, with a compound of formula IV: **(See formula)** where R9 and R10 are as defined above; (d) cyclizing a compound XII in which two pairs of -OH groups and: **(See formula)** where R9 and R10 are as defined above, and Y is a group -OH or a group -NL1L2, where L1 and L2 are the same or different, are each hydrogen, phenyl, lower alcohol, or together form a chain of 4- or 5-membered alcoholylene, saturated or unsaturated, are attached to two pairs of ortho positions of a benzene or naphthalene nucleus; or (e) selectively dehydrogenating a compound XIII in which two chains of formula XXf: **(See formula)** where R9 and R10 are as defined above, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus; or (f) produce a compound (to be called an If compound) in which two chains of formula XXh: **(See formula)** they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus, removing both R11 groups from a compound (to be called a compound XVII) in which two chains of formula XXi: **(See formula)** where R11 is as defined above, they are attached to two pairs of ortho positions of a benzene or naphthalene nucleus; and, if desired or necessary, converting compound I to a pharmaceutically acceptable derivative thereof, or vice versa. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5599772 | 1972-12-05 | ||
| GB3904773 | 1973-08-17 | ||
| GB3904673*[A GB1449810A (en) | 1972-12-05 | 1973-08-17 | Benzo-or naphtho-dipyran-di-n-tetrazolyl- -carboxamide derivative methods for their production and compositions containing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES421132A1 true ES421132A1 (en) | 1976-04-16 |
Family
ID=27259543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES421132A Expired ES421132A1 (en) | 1972-12-05 | 1973-12-04 | Benzo-or naphtho-dipyran-di-n-tetrazolyl- -carboxamide derivative methods for their production and compositions containing them |
Country Status (17)
| Country | Link |
|---|---|
| JP (1) | JPS4993366A (en) |
| AR (1) | AR210310A1 (en) |
| CH (1) | CH593277A5 (en) |
| DD (1) | DD109387A5 (en) |
| DE (1) | DE2360331A1 (en) |
| ES (1) | ES421132A1 (en) |
| FR (1) | FR2208670B1 (en) |
| GB (1) | GB1449810A (en) |
| IE (1) | IE38544B1 (en) |
| IL (1) | IL43709A (en) |
| LU (1) | LU68934A1 (en) |
| MW (1) | MW6873A1 (en) |
| NL (1) | NL7316658A (en) |
| NO (1) | NO141517C (en) |
| PL (1) | PL102530B1 (en) |
| SE (1) | SE409205B (en) |
| SU (1) | SU553934A3 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4792547A (en) * | 1985-12-26 | 1988-12-20 | Hokuriku Pharmaceutical Co., Ltd. | Pyrazine-2-carboxamide derivatives useful in treating allergic disease |
| EP1358868A3 (en) * | 2002-04-23 | 2003-11-19 | L'oreal | Cosmetic composition for increasing hair growth and/or for preventing or delaying hair loss |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1354477A (en) * | 1970-04-02 | 1974-06-05 | Fisons Ltd | Benzo di and tri-pyrones |
| GB1321879A (en) * | 1970-12-30 | 1973-07-04 | Fisons Ltd | Di-carboxybenzopyrano-benzopyrans |
| BE789822A (en) * | 1971-10-08 | 1973-04-06 | Allen & Hanburys Ltd | NEW HETEROCYCLIC COMPOUNDS |
-
1973
- 1973-08-17 GB GB3904673*[A patent/GB1449810A/en not_active Expired
- 1973-11-23 IE IE2129/73A patent/IE38544B1/en unknown
- 1973-11-27 MW MW68/73*UA patent/MW6873A1/en unknown
- 1973-11-27 IL IL43709A patent/IL43709A/en unknown
- 1973-12-03 FR FR7342955A patent/FR2208670B1/fr not_active Expired
- 1973-12-04 ES ES421132A patent/ES421132A1/en not_active Expired
- 1973-12-04 PL PL1973167040A patent/PL102530B1/en unknown
- 1973-12-04 NO NO4629/73A patent/NO141517C/en unknown
- 1973-12-04 DE DE2360331A patent/DE2360331A1/en not_active Withdrawn
- 1973-12-04 CH CH1694773A patent/CH593277A5/xx not_active IP Right Cessation
- 1973-12-04 SU SU1977568A patent/SU553934A3/en active
- 1973-12-04 LU LU68934A patent/LU68934A1/xx unknown
- 1973-12-04 SE SE7316373A patent/SE409205B/en unknown
- 1973-12-05 DD DD175118A patent/DD109387A5/xx unknown
- 1973-12-05 NL NL7316658A patent/NL7316658A/xx not_active Application Discontinuation
- 1973-12-05 JP JP48135465A patent/JPS4993366A/ja active Pending
-
1976
- 1976-12-04 AR AR251356A patent/AR210310A1/en active
Also Published As
| Publication number | Publication date |
|---|---|
| AR210310A1 (en) | 1977-07-29 |
| NO141517C (en) | 1980-03-26 |
| AU6305073A (en) | 1975-05-29 |
| IE38544B1 (en) | 1978-04-12 |
| NL7316658A (en) | 1974-06-07 |
| IL43709A (en) | 1977-04-29 |
| SU553934A3 (en) | 1977-04-05 |
| SE409205B (en) | 1979-08-06 |
| FR2208670B1 (en) | 1978-01-13 |
| IE38544L (en) | 1974-06-05 |
| JPS4993366A (en) | 1974-09-05 |
| DE2360331A1 (en) | 1974-06-06 |
| GB1449810A (en) | 1976-09-15 |
| NO141517B (en) | 1979-12-17 |
| CH593277A5 (en) | 1977-11-30 |
| PL102530B1 (en) | 1979-04-30 |
| DD109387A5 (en) | 1974-11-05 |
| LU68934A1 (en) | 1974-07-05 |
| IL43709A0 (en) | 1974-03-14 |
| MW6873A1 (en) | 1974-07-10 |
| FR2208670A1 (en) | 1974-06-28 |
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