GB1143999A - Aminoalkyl-dihydroethanoanthracenes and process for their manufacture - Google Patents
Aminoalkyl-dihydroethanoanthracenes and process for their manufactureInfo
- Publication number
- GB1143999A GB1143999A GB5555366A GB5555366A GB1143999A GB 1143999 A GB1143999 A GB 1143999A GB 5555366 A GB5555366 A GB 5555366A GB 5555366 A GB5555366 A GB 5555366A GB 1143999 A GB1143999 A GB 1143999A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloro
- anthryl
- group
- acid
- propionic acid
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 8
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 235000019260 propionic acid Nutrition 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- -1 monomethylamino Chemical group 0.000 abstract 2
- BVDRUNQRQNOFHR-UHFFFAOYSA-N (2-chloroanthracen-9-yl)methanol Chemical compound C1=C(Cl)C=C2C(CO)=C(C=CC=C3)C3=CC2=C1 BVDRUNQRQNOFHR-UHFFFAOYSA-N 0.000 abstract 1
- KGMDODIDEQTIRA-UHFFFAOYSA-N 1,2-dihydrocyclobuta[a]anthracene Chemical compound C1=CC2=CC3=CC=CC=C3C=C2C2=C1CC2 KGMDODIDEQTIRA-UHFFFAOYSA-N 0.000 abstract 1
- UBLKZPDYDFGLBZ-UHFFFAOYSA-N 2-[(2-chloroanthracen-9-yl)methyl]propanedioic acid Chemical compound ClC1=CC2=C(C3=CC=CC=C3C=C2C=C1)CC(C(=O)O)C(=O)O UBLKZPDYDFGLBZ-UHFFFAOYSA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- VHNJYJXDQKORPF-UHFFFAOYSA-N 2-chloroanthracene-9-carbaldehyde Chemical compound C1=CC=CC2=C(C=O)C3=CC(Cl)=CC=C3C=C21 VHNJYJXDQKORPF-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910010082 LiAlH Inorganic materials 0.000 abstract 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical class NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- ZHZJDZVNAPXUGH-UHFFFAOYSA-N diethyl 2-[(2-chloroanthracen-9-yl)methyl]propanedioate Chemical compound C(C)OC(=O)C(CC=1C2=CC=CC=C2C=C2C=CC(=CC12)Cl)C(=O)OCC ZHZJDZVNAPXUGH-UHFFFAOYSA-N 0.000 abstract 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 230000006203 ethylation Effects 0.000 abstract 1
- 238000006200 ethylation reaction Methods 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 230000011987 methylation Effects 0.000 abstract 1
- 238000007069 methylation reaction Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 230000000506 psychotropic effect Effects 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 238000006722 reduction reaction Methods 0.000 abstract 1
- 238000005932 reductive alkylation reaction Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000932 sedative agent Substances 0.000 abstract 1
- 230000001624 sedative effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
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 |
|---|---|---|---|
| CH1708665A CH448069A (de) | 1960-11-29 | 1965-12-10 | Verfahren zur Herstellung neuer Amine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1143999A true GB1143999A (en) | 1969-02-26 |
Family
ID=4422644
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5555466A Expired GB1149557A (en) | 1965-12-10 | 1966-12-12 | Aminoalkyl-dihydroethanoanthracenes and process for their manufacture |
| GB5555366A Expired GB1143999A (en) | 1965-12-10 | 1966-12-12 | Aminoalkyl-dihydroethanoanthracenes and process for their manufacture |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5555466A Expired GB1149557A (en) | 1965-12-10 | 1966-12-12 | Aminoalkyl-dihydroethanoanthracenes and process for their manufacture |
Country Status (11)
| Country | Link |
|---|---|
| AT (12) | AT278766B (enrdf_load_stackoverflow) |
| BE (3) | BE690940A (enrdf_load_stackoverflow) |
| BR (3) | BR6685266D0 (enrdf_load_stackoverflow) |
| DE (1) | DE1568355A1 (enrdf_load_stackoverflow) |
| DK (3) | DK130176B (enrdf_load_stackoverflow) |
| FR (6) | FR6353M (enrdf_load_stackoverflow) |
| GB (2) | GB1149557A (enrdf_load_stackoverflow) |
| GT (1) | GT197119100A (enrdf_load_stackoverflow) |
| NL (3) | NL6617368A (enrdf_load_stackoverflow) |
| SE (2) | SE354850B (enrdf_load_stackoverflow) |
| SU (4) | SU424348A3 (enrdf_load_stackoverflow) |
-
1966
- 1966-12-02 DE DE19661568355 patent/DE1568355A1/de active Pending
- 1966-12-09 BE BE690940A patent/BE690940A/xx unknown
- 1966-12-09 AT AT1966A patent/AT278766B/de not_active IP Right Cessation
- 1966-12-09 AT AT1135366A patent/AT272326B/de active
- 1966-12-09 DK DK638866A patent/DK130176B/da unknown
- 1966-12-09 AT AT1135566A patent/AT272327B/de active
- 1966-12-09 AT AT173868A patent/AT272328B/de active
- 1966-12-09 AT AT1135266A patent/AT271459B/de active
- 1966-12-09 AT AT196468A patent/AT273084B/de active
- 1966-12-09 AT AT174068A patent/AT271462B/de active
- 1966-12-09 BR BR18526666A patent/BR6685266D0/pt unknown
- 1966-12-09 AT AT174168A patent/AT271463B/de active
- 1966-12-09 NL NL6617368A patent/NL6617368A/xx unknown
- 1966-12-09 AT AT173468A patent/AT273946B/de active
- 1966-12-09 BR BR18526866A patent/BR6685268D0/pt unknown
- 1966-12-09 BE BE690941D patent/BE690941A/xx unknown
- 1966-12-09 BR BR18526766A patent/BR6685267D0/pt unknown
- 1966-12-09 DK DK638666A patent/DK130786B/da unknown
- 1966-12-09 DK DK638766A patent/DK130175B/da unknown
- 1966-12-09 AT AT173968A patent/AT276364B/de active
- 1966-12-09 SE SE1690766A patent/SE354850B/xx unknown
- 1966-12-09 AT AT173568A patent/AT271461B/de active
- 1966-12-09 NL NL6617369A patent/NL6617369A/xx unknown
- 1966-12-09 AT AT196568A patent/AT273085B/de active
- 1966-12-09 BE BE690939D patent/BE690939A/xx unknown
- 1966-12-09 SE SE1690666A patent/SE324788B/xx unknown
- 1966-12-09 NL NL6617367A patent/NL6617367A/xx unknown
- 1966-12-10 SU SU1717552A patent/SU424348A3/ru active
- 1966-12-10 SU SU1118632A patent/SU414785A3/ru active
- 1966-12-12 GB GB5555466A patent/GB1149557A/en not_active Expired
- 1966-12-12 GB GB5555366A patent/GB1143999A/en not_active Expired
-
1967
- 1967-03-02 FR FR97136A patent/FR6353M/fr not_active Expired
- 1967-03-02 FR FR97135A patent/FR6436M/fr not_active Expired
- 1967-03-02 FR FR97138A patent/FR6355M/fr not_active Expired
- 1967-03-02 FR FR97140A patent/FR6357M/fr not_active Expired
- 1967-03-02 FR FR97137A patent/FR6354M/fr not_active Expired
- 1967-03-02 FR FR97139A patent/FR6356M/fr not_active Expired
-
1971
- 1971-01-18 GT GT197119100A patent/GT197119100A/es unknown
- 1971-11-24 SU SU1717378A patent/SU549076A3/ru active
- 1971-11-24 SU SU1717390A patent/SU549077A3/ru active
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