SU424348A3 - - Google Patents
Info
- Publication number
- SU424348A3 SU424348A3 SU1717552A SU1717552A SU424348A3 SU 424348 A3 SU424348 A3 SU 424348A3 SU 1717552 A SU1717552 A SU 1717552A SU 1717552 A SU1717552 A SU 1717552A SU 424348 A3 SU424348 A3 SU 424348A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- formula
- compounds
- ethanoanthracene
- ethano
- residue
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 description 5
- KGMDODIDEQTIRA-UHFFFAOYSA-N 1,2-dihydrocyclobuta[a]anthracene Chemical compound C1=CC2=CC3=CC=CC=C3C=C2C2=C1CC2 KGMDODIDEQTIRA-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- WPDAVTSOEQEGMS-UHFFFAOYSA-N 9,10-dihydroanthracene Chemical class C1=CC=C2CC3=CC=CC=C3CC2=C1 WPDAVTSOEQEGMS-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000005698 Diels-Alder reaction Methods 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000003335 secondary amines Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 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 |
|---|---|
| SU424348A3 true SU424348A3 (cg-RX-API-DMAC7.html) | 1974-04-15 |
Family
ID=4422644
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1118632A SU414785A3 (ru) | 1965-12-10 | 1966-12-10 | Способ получения этаноантраценов |
| SU1717552A SU424348A3 (cg-RX-API-DMAC7.html) | 1965-12-10 | 1966-12-10 | |
| SU1717390A SU549077A3 (ru) | 1965-12-10 | 1971-11-24 | Способ получени аминоэтаноантраценов или их солей |
| SU1717378A SU549076A3 (ru) | 1965-12-10 | 1971-11-24 | Способ получени аминоэтаноантрацентов или их солей |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1118632A SU414785A3 (ru) | 1965-12-10 | 1966-12-10 | Способ получения этаноантраценов |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1717390A SU549077A3 (ru) | 1965-12-10 | 1971-11-24 | Способ получени аминоэтаноантраценов или их солей |
| SU1717378A SU549076A3 (ru) | 1965-12-10 | 1971-11-24 | Способ получени аминоэтаноантрацентов или их солей |
Country Status (11)
| Country | Link |
|---|---|
| AT (12) | AT272326B (cg-RX-API-DMAC7.html) |
| BE (3) | BE690939A (cg-RX-API-DMAC7.html) |
| BR (3) | BR6685268D0 (cg-RX-API-DMAC7.html) |
| DE (1) | DE1568355A1 (cg-RX-API-DMAC7.html) |
| DK (3) | DK130176B (cg-RX-API-DMAC7.html) |
| FR (6) | FR6357M (cg-RX-API-DMAC7.html) |
| GB (2) | GB1143999A (cg-RX-API-DMAC7.html) |
| GT (1) | GT197119100A (cg-RX-API-DMAC7.html) |
| NL (3) | NL6617368A (cg-RX-API-DMAC7.html) |
| SE (2) | SE324788B (cg-RX-API-DMAC7.html) |
| SU (4) | SU414785A3 (cg-RX-API-DMAC7.html) |
-
1966
- 1966-12-02 DE DE19661568355 patent/DE1568355A1/de active Pending
- 1966-12-09 AT AT1135366A patent/AT272326B/de active
- 1966-12-09 DK DK638866A patent/DK130176B/da unknown
- 1966-12-09 NL NL6617368A patent/NL6617368A/xx unknown
- 1966-12-09 AT AT174068A patent/AT271462B/de active
- 1966-12-09 BE BE690939D patent/BE690939A/xx unknown
- 1966-12-09 BR BR18526866A patent/BR6685268D0/pt unknown
- 1966-12-09 AT AT173568A patent/AT271461B/de active
- 1966-12-09 AT AT173868A patent/AT272328B/de active
- 1966-12-09 AT AT1135266A patent/AT271459B/de active
- 1966-12-09 DK DK638666A patent/DK130786B/da unknown
- 1966-12-09 AT AT1135566A patent/AT272327B/de active
- 1966-12-09 AT AT173968A patent/AT276364B/de active
- 1966-12-09 AT AT1966A patent/AT278766B/de not_active IP Right Cessation
- 1966-12-09 BR BR18526766A patent/BR6685267D0/pt unknown
- 1966-12-09 AT AT173468A patent/AT273946B/de active
- 1966-12-09 DK DK638766A patent/DK130175B/da unknown
- 1966-12-09 AT AT174168A patent/AT271463B/de active
- 1966-12-09 SE SE1690666A patent/SE324788B/xx unknown
- 1966-12-09 BE BE690941D patent/BE690941A/xx unknown
- 1966-12-09 AT AT196568A patent/AT273085B/de active
- 1966-12-09 BR BR18526666A patent/BR6685266D0/pt unknown
- 1966-12-09 NL NL6617369A patent/NL6617369A/xx unknown
- 1966-12-09 BE BE690940A patent/BE690940A/xx unknown
- 1966-12-09 SE SE1690766A patent/SE354850B/xx unknown
- 1966-12-09 NL NL6617367A patent/NL6617367A/xx unknown
- 1966-12-09 AT AT196468A patent/AT273084B/de active
- 1966-12-10 SU SU1118632A patent/SU414785A3/ru active
- 1966-12-10 SU SU1717552A patent/SU424348A3/ru active
- 1966-12-12 GB GB5555366A patent/GB1143999A/en not_active Expired
- 1966-12-12 GB GB5555466A patent/GB1149557A/en not_active Expired
-
1967
- 1967-03-02 FR FR97140A patent/FR6357M/fr not_active Expired
- 1967-03-02 FR FR97136A patent/FR6353M/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
- 1967-03-02 FR FR97135A patent/FR6436M/fr not_active Expired
- 1967-03-02 FR FR97138A patent/FR6355M/fr not_active Expired
-
1971
- 1971-01-18 GT GT197119100A patent/GT197119100A/es unknown
- 1971-11-24 SU SU1717390A patent/SU549077A3/ru active
- 1971-11-24 SU SU1717378A patent/SU549076A3/ru active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Cope et al. | Rearrangement of oxime N-ethers | |
| US2608584A (en) | Preparation of n-alkyl arylamines | |
| GB1452466A (en) | Process for the production of aniline and apparatus therefor | |
| SU417936A3 (cg-RX-API-DMAC7.html) | ||
| US3287411A (en) | Process of making aliphatic amines | |
| SU424348A3 (cg-RX-API-DMAC7.html) | ||
| US3442950A (en) | Process for preparing an aminated benzene | |
| US2573644A (en) | beta-chloroethyl aminoindanes | |
| US3078275A (en) | N, n-disubstituted-alpha-(tertiaryaminoalkyl)-alpha, alpha-diphenylacetamides | |
| CA1217485A (fr) | Amino-2 aminomethyl-5 oxazolines-2, leur methode de preparation ainsi que leur application therapeutique | |
| Heinzelman et al. | Compounds containing the pyrrolidine ring. Analogs of sympathomimetic amines | |
| US3156725A (en) | Substituted 2-phenoxy and phenylthio-cyclopropylamines | |
| US2683735A (en) | Aromatic esters of basically substituted isocyclyl carbamates | |
| GB915430A (en) | Synthesis of carbazoles | |
| ES411826A1 (es) | Procedimiento de obtencion de 1-ariloxi - 2 - propanolami- nas farmacologicamente activos. | |
| US3532722A (en) | Spiro(dibenzo(a,d) (1,4) cycloheptadiene-5-4' - tetrahydrofurfurylamine) and mono- and dialkylated derivatives and their salts | |
| Mukai | Reaction of 2-Chloro-3-phenyltropone and 2-Chloro-7-phenyltropone with Ammonia and Amines | |
| US3484457A (en) | Certain spiro butyrolactones | |
| US2828340A (en) | Hydroxy-lower-alkyl-bis(cyclohexylpropyl) amines, salts thereof, and preparation thereof | |
| Kulkarni et al. | 2, 6-Diboraadamantane, a novel structure with unusual characteristics, via cyclic dihydroboration of 1, 3, 5, 7-cyclooctatetraene | |
| Shirley et al. | Nitrogen Mustard Derivatives of Phenothiazine and Phenoxazine | |
| ES394761A1 (es) | Un metodo de preparar un derivado de 2-amino-1,5-benzodia- zocina. | |
| ES477848A1 (es) | Procedimiento para la produccion de feniletilamina. | |
| US3040028A (en) | Process for separating 1-methylhomopiperazine and homopiperazine | |
| US3896133A (en) | Substituted 10-heterocyclicaminoalkyl-9,10-dihydroanthracenes |