CA1053680A - Derivatives of tetralone and the preparation thereof - Google Patents
Derivatives of tetralone and the preparation thereofInfo
- Publication number
- CA1053680A CA1053680A CA235,691A CA235691A CA1053680A CA 1053680 A CA1053680 A CA 1053680A CA 235691 A CA235691 A CA 235691A CA 1053680 A CA1053680 A CA 1053680A
- Authority
- CA
- Canada
- Prior art keywords
- formula
- process according
- tetraline
- amino
- 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
- 238000002360 preparation method Methods 0.000 title abstract description 7
- XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical class C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 20
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 4
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 4
- 150000001412 amines Chemical class 0.000 claims description 10
- MUGWUYGVUZLWRB-SECBINFHSA-N (2r)-2-amino-3,4-dihydro-2h-naphthalen-1-one Chemical class C1=CC=C2C(=O)[C@H](N)CCC2=C1 MUGWUYGVUZLWRB-SECBINFHSA-N 0.000 claims description 6
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
- AYNCWMIFKFADCZ-UHFFFAOYSA-N 2-bromo-3,4-dihydro-2h-naphthalen-1-one Chemical compound C1=CC=C2C(=O)C(Br)CCC2=C1 AYNCWMIFKFADCZ-UHFFFAOYSA-N 0.000 claims description 4
- -1 2-(p-methoxyphenylamino)-tetraline-1-one Chemical compound 0.000 claims 3
- CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 claims 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 claims 1
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 claims 1
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 claims 1
- LCGFVWKNXLRFIF-SNVBAGLBSA-N (2r)-1,2,3,4-tetrahydronaphthalen-2-amine Chemical class C1=CC=C2C[C@H](N)CCC2=C1 LCGFVWKNXLRFIF-SNVBAGLBSA-N 0.000 abstract description 5
- 239000000543 intermediate Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000376 reactant Substances 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000006722 reduction reaction Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000875 corresponding effect Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- ZKLQKLNCMKDIDO-UHFFFAOYSA-N 2-anilino-3,4-dihydro-2h-naphthalen-1-one Chemical compound C1CC2=CC=CC=C2C(=O)C1NC1=CC=CC=C1 ZKLQKLNCMKDIDO-UHFFFAOYSA-N 0.000 description 2
- ICGLPKIVTVWCFT-UHFFFAOYSA-N 4-methylbenzenesulfonohydrazide Chemical compound CC1=CC=C(S(=O)(=O)NN)C=C1 ICGLPKIVTVWCFT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZDQWVKDDJDIVAL-UHFFFAOYSA-N catecholborane Chemical compound C1=CC=C2O[B]OC2=C1 ZDQWVKDDJDIVAL-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QFNABHBYVSJWLO-UHFFFAOYSA-N 3,4,4a,5-tetrahydro-2h-naphthalen-1-one Chemical compound C1C=CC=C2C(=O)CCCC21 QFNABHBYVSJWLO-UHFFFAOYSA-N 0.000 description 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
- 229910018954 NaNH2 Inorganic materials 0.000 description 1
- 241000786363 Rhampholeon spectrum Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 238000005644 Wolff-Kishner reduction reaction Methods 0.000 description 1
- 239000000538 analytical sample Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- LSDXVUJCUPTXIN-UHFFFAOYSA-N n-phenyl-1,2,3,4-tetrahydronaphthalen-2-amine Chemical compound C1CC2=CC=CC=C2CC1NC1=CC=CC=C1 LSDXVUJCUPTXIN-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/20—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
-
- 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)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB40296/74A GB1488851A (en) | 1974-09-16 | 1974-09-16 | 2-amino-tetralin-1-ones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1053680A true CA1053680A (en) | 1979-05-01 |
Family
ID=10414188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA235,691A Expired CA1053680A (en) | 1974-09-16 | 1975-09-12 | Derivatives of tetralone and the preparation thereof |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US3970650A (OSRAM) |
| JP (1) | JPS5156437A (OSRAM) |
| AR (1) | AR206644A1 (OSRAM) |
| AT (1) | AT337676B (OSRAM) |
| BE (1) | BE833217A (OSRAM) |
| CA (1) | CA1053680A (OSRAM) |
| CH (1) | CH593237A5 (OSRAM) |
| DD (1) | DD122968A5 (OSRAM) |
| DE (1) | DE2541012A1 (OSRAM) |
| ES (1) | ES440950A1 (OSRAM) |
| FR (1) | FR2284588A1 (OSRAM) |
| GB (1) | GB1488851A (OSRAM) |
| HU (1) | HU173048B (OSRAM) |
| IL (1) | IL48097A0 (OSRAM) |
| LU (1) | LU73406A1 (OSRAM) |
| NL (1) | NL7510829A (OSRAM) |
| SE (1) | SE7510272L (OSRAM) |
| ZA (1) | ZA755758B (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4975461A (en) * | 1986-06-19 | 1990-12-04 | E. R. Squibb & Sons, Inc. | P-aminophenols, derivatives thereof and method of use |
| US5891459A (en) * | 1993-06-11 | 1999-04-06 | The Board Of Trustees Of The Leland Stanford Junior University | Enhancement of vascular function by modulation of endogenous nitric oxide production or activity |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR768604A (fr) | 1933-02-13 | 1934-08-10 | Procédé de transformation des composés céto-méthyléniques en composés céto-aminés | |
| US2647123A (en) * | 1951-10-11 | 1953-07-28 | Research Corp | Nu-(2-pyridyl) 2-chloro-3-amino-1, 4-naphthoquinones |
-
1974
- 1974-09-16 GB GB40296/74A patent/GB1488851A/en not_active Expired
-
1975
- 1975-01-01 AR AR260359A patent/AR206644A1/es active
- 1975-09-09 ZA ZA00755758A patent/ZA755758B/xx unknown
- 1975-09-09 BE BE159864A patent/BE833217A/xx unknown
- 1975-09-12 FR FR7528102A patent/FR2284588A1/fr active Granted
- 1975-09-12 CA CA235,691A patent/CA1053680A/en not_active Expired
- 1975-09-12 IL IL48097A patent/IL48097A0/xx unknown
- 1975-09-12 HU HU75CI1064A patent/HU173048B/hu unknown
- 1975-09-13 DE DE19752541012 patent/DE2541012A1/de active Pending
- 1975-09-13 JP JP50111568A patent/JPS5156437A/ja active Pending
- 1975-09-15 LU LU73406A patent/LU73406A1/xx unknown
- 1975-09-15 SE SE7510272A patent/SE7510272L/xx unknown
- 1975-09-15 NL NL7510829A patent/NL7510829A/xx not_active Application Discontinuation
- 1975-09-15 CH CH1189975A patent/CH593237A5/xx not_active IP Right Cessation
- 1975-09-15 ES ES440950A patent/ES440950A1/es not_active Expired
- 1975-09-16 DD DD188374A patent/DD122968A5/xx unknown
- 1975-09-16 AT AT709175A patent/AT337676B/de active
- 1975-09-16 US US05/613,828 patent/US3970650A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DD122968A5 (de) | 1976-11-12 |
| NL7510829A (nl) | 1976-03-18 |
| CH593237A5 (OSRAM) | 1977-11-30 |
| AT337676B (de) | 1977-07-11 |
| JPS5156437A (en) | 1976-05-18 |
| GB1488851A (en) | 1977-10-12 |
| AR206644A1 (es) | 1976-08-06 |
| ATA709175A (de) | 1976-11-15 |
| BE833217A (fr) | 1976-03-09 |
| DE2541012A1 (de) | 1976-04-22 |
| IL48097A0 (en) | 1975-11-25 |
| AU8486375A (en) | 1977-03-31 |
| ES440950A1 (es) | 1977-03-16 |
| SE7510272L (sv) | 1976-03-17 |
| HU173048B (hu) | 1979-02-28 |
| LU73406A1 (OSRAM) | 1976-04-13 |
| ZA755758B (en) | 1976-08-25 |
| FR2284588A1 (fr) | 1976-04-09 |
| US3970650A (en) | 1976-07-20 |
| FR2284588B1 (OSRAM) | 1978-04-07 |
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