GB1149557A - Aminoalkyl-dihydroethanoanthracenes and process for their manufacture - Google Patents
Aminoalkyl-dihydroethanoanthracenes and process for their manufactureInfo
- Publication number
- GB1149557A GB1149557A GB5555466A GB5555466A GB1149557A GB 1149557 A GB1149557 A GB 1149557A GB 5555466 A GB5555466 A GB 5555466A GB 5555466 A GB5555466 A GB 5555466A GB 1149557 A GB1149557 A GB 1149557A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- ethano
- anthracene
- compound
- dimethylaminomethyl
- 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
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000006264 diethylaminomethyl group Chemical group [H]C([H])([H])C([H])([H])N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 abstract 3
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- KGMDODIDEQTIRA-UHFFFAOYSA-N 1,2-dihydrocyclobuta[a]anthracene Chemical compound C1=CC2=CC3=CC=CC=C3C=C2C2=C1CC2 KGMDODIDEQTIRA-UHFFFAOYSA-N 0.000 abstract 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 239000003638 chemical reducing agent Substances 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 abstract 1
- OWFINXQLBMJDJQ-UHFFFAOYSA-N 2-chloroanthracene Chemical compound C1=CC=CC2=CC3=CC(Cl)=CC=C3C=C21 OWFINXQLBMJDJQ-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 229910010082 LiAlH Inorganic materials 0.000 abstract 1
- -1 N-acetyl compound Chemical class 0.000 abstract 1
- 239000007868 Raney catalyst Substances 0.000 abstract 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 1
- 229910000564 Raney nickel Inorganic materials 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 abstract 1
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 abstract 1
- CMBLOUYWEHGGES-UHFFFAOYSA-N anthracene;hydrochloride Chemical compound Cl.C1=CC=CC2=CC3=CC=CC=C3C=C21 CMBLOUYWEHGGES-UHFFFAOYSA-N 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 229940117389 dichlorobenzene Drugs 0.000 abstract 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000006534 ethyl amino methyl group Chemical group [H]N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 229910052987 metal hydride Inorganic materials 0.000 abstract 1
- 150000004681 metal hydrides Chemical class 0.000 abstract 1
- 125000006533 methyl amino methyl group Chemical group [H]N(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 230000004048 modification Effects 0.000 abstract 1
- 238000012986 modification Methods 0.000 abstract 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 229910003446 platinum oxide Inorganic materials 0.000 abstract 1
- YBTMSVKMINMVAZ-UHFFFAOYSA-N pocl3 benzene Chemical compound ClP(Cl)(Cl)=O.C1=CC=CC=C1 YBTMSVKMINMVAZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000000506 psychotropic effect Effects 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 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 |
---|---|
GB1149557A true GB1149557A (en) | 1969-04-23 |
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 After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5555366A Expired GB1143999A (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
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2187745A (en) | Process for hydrogenating amides and imides to amines | |
CA2057637A1 (en) | Process for the preparation of saturated primary fatty amines by hydrogenation of unsaturated fatty acid nitriles | |
GB1298214A (en) | A process for the manufacture of 19-norsteroids | |
US3884936A (en) | Preparation of 2-pyrrolidone | |
GB1149557A (en) | Aminoalkyl-dihydroethanoanthracenes and process for their manufacture | |
US3812148A (en) | Preparation of 2-pyrrolidone | |
GB864926A (en) | Process for preparing novel compounds of the lactone type | |
US3673187A (en) | Bis-(dihydroxyphenyl-ethylol)-substituted alkylenediamines and the salts thereof | |
US2109159A (en) | Process for preparing furfurylamines | |
GB1494823A (en) | Process for the production of 2-aryl-2h-benzotriazoles | |
GB1475486A (en) | Process for the production of gamma-butyrolactone | |
US3812149A (en) | Preparation of 2-pyrrolidinone | |
US2623886A (en) | Process for conversion of estrone compounds to estradiol compounds | |
US2522858A (en) | Hydrogenation of streptomycin | |
US3855237A (en) | Process of making hexahydro-1h-furo(3,4-c) pyrrole | |
GB599016A (en) | Improvements in or relating to the production of ribitylaminobenzenes and triacyl derivatives thereof | |
GB1106088A (en) | Process for the preparation of phloroglucinol | |
CA1050570A (en) | Cyclopropylmethylamine derivatives | |
ES251102A1 (es) | Procedimiento para preparar la amida del acido 7-ciano-2,5-heptadienoico | |
US2346027A (en) | Process for the manufacture of aryl-alicyclic fatty acid esters | |
GB730608A (en) | Process for the preparation of -amino-ª†-ketocaproic acid | |
GB596539A (en) | New heterocyclic compounds | |
US2175003A (en) | Process for the preparation of hexahydro-para-phenylene diamine | |
GB1368545A (en) | Preparation of dihydrocoumarin and of alkyl derivatives thereof | |
GB930676A (en) | Process for the preparation of 20-alkylamino steroid derivatives and novel 20-alkylamino steroid derivatives prepared thereby |