NO743782L - - Google Patents
Info
- Publication number
- NO743782L NO743782L NO743782A NO743782A NO743782L NO 743782 L NO743782 L NO 743782L NO 743782 A NO743782 A NO 743782A NO 743782 A NO743782 A NO 743782A NO 743782 L NO743782 L NO 743782L
- Authority
- NO
- Norway
- Prior art keywords
- lower alkyl
- hydrogen
- benzodiazepine
- halogen
- general formula
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 claims description 4
- 229940049706 benzodiazepine Drugs 0.000 claims description 4
- 150000007857 hydrazones Chemical class 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- WHYAIKHHRCPZBI-UHFFFAOYSA-N 8-chloro-1-methyl-5-oxido-6-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-5-ium Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2C[N+]([O-])=C1C1=CC=CC=C1 WHYAIKHHRCPZBI-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 238000007363 ring formation reaction Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 235000019439 ethyl acetate Nutrition 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 125000002587 enol group Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 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 3
- GWSXDWFXNVOIIC-UHFFFAOYSA-N (7-chloro-5-phenyl-3h-1,4-benzodiazepin-2-yl)hydrazine Chemical compound N=1CC(NN)=NC2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 GWSXDWFXNVOIIC-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- KYTREVLPRJOBEM-UHFFFAOYSA-N triazolo[4,5-i][1,2]benzodiazepine Chemical compound C1=CC2=CC=CN=NC2=C2C1=NN=N2 KYTREVLPRJOBEM-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- HDQYKTQKHDIKRF-UHFFFAOYSA-N 1,2-benzodiazepin-2-ylhydrazine Chemical compound NNN1C=CC=C2C=CC=CC2=N1 HDQYKTQKHDIKRF-UHFFFAOYSA-N 0.000 description 1
- GSIGZZKHXAAYOA-UHFFFAOYSA-N 6-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine Chemical class C12=CC=CC=C2N2C=NN=C2CN=C1C1=CC=CC=C1 GSIGZZKHXAAYOA-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- YWDMPPYKVLCSCK-UHFFFAOYSA-N [O-][N+]=1CC(NN)=NC2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 Chemical compound [O-][N+]=1CC(NN)=NC2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 YWDMPPYKVLCSCK-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 description 1
- 150000001557 benzodiazepines Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- DGCTVLNZTFDPDJ-UHFFFAOYSA-N heptane-3,5-dione Chemical compound CCC(=O)CC(=O)CC DGCTVLNZTFDPDJ-UHFFFAOYSA-N 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- -1 methoxy, ethoxy, propoxy Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229940125723 sedative agent Drugs 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003204 tranquilizing agent Substances 0.000 description 1
- 230000002936 tranquilizing effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US408245A US3864328A (en) | 1973-10-19 | 1973-10-19 | 2-hydrazino benzodiazepine derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO743782L true NO743782L (xx) | 1975-05-20 |
Family
ID=23615471
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO743782A NO743782L (xx) | 1973-10-19 | 1974-10-18 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US3864328A (xx) |
| JP (1) | JPS5064299A (xx) |
| AR (1) | AR202848A1 (xx) |
| AU (1) | AU7449174A (xx) |
| BE (1) | BE821221A (xx) |
| DD (1) | DD115674A5 (xx) |
| DE (1) | DE2447776A1 (xx) |
| DK (1) | DK521074A (xx) |
| ES (1) | ES431124A1 (xx) |
| FI (1) | FI296574A (xx) |
| FR (1) | FR2250757B1 (xx) |
| GB (1) | GB1428085A (xx) |
| IE (1) | IE39948B1 (xx) |
| IL (1) | IL45863A0 (xx) |
| LU (1) | LU71132A1 (xx) |
| NL (1) | NL7413535A (xx) |
| NO (1) | NO743782L (xx) |
| SE (1) | SE7413067L (xx) |
| ZA (1) | ZA745987B (xx) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4086230A (en) * | 1977-03-09 | 1978-04-25 | The Upjohn Company | 1,5-Dihydro-7-aryl-as-triazine[4,3,-α][1,4]benzodiazepin-1-ols |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PH9315A (en) * | 1968-11-05 | 1975-08-22 | K Meguro | Triazolo(4,3-a)(1,4)benzodiazepine derivatives |
-
1973
- 1973-10-19 US US408245A patent/US3864328A/en not_active Expired - Lifetime
-
1974
- 1974-09-20 ZA ZA00745987A patent/ZA745987B/xx unknown
- 1974-10-03 DK DK521074A patent/DK521074A/da unknown
- 1974-10-07 DE DE19742447776 patent/DE2447776A1/de active Pending
- 1974-10-11 FI FI2965/74A patent/FI296574A/fi unknown
- 1974-10-15 NL NL7413535A patent/NL7413535A/xx unknown
- 1974-10-16 SE SE7413067A patent/SE7413067L/xx unknown
- 1974-10-17 IE IE2136/74A patent/IE39948B1/xx unknown
- 1974-10-17 LU LU71132A patent/LU71132A1/xx unknown
- 1974-10-17 IL IL45863A patent/IL45863A0/xx unknown
- 1974-10-17 FR FR7434920A patent/FR2250757B1/fr not_active Expired
- 1974-10-18 BE BE149657A patent/BE821221A/xx unknown
- 1974-10-18 ES ES431124A patent/ES431124A1/es not_active Expired
- 1974-10-18 NO NO743782A patent/NO743782L/no unknown
- 1974-10-18 AU AU74491/74A patent/AU7449174A/en not_active Expired
- 1974-10-18 AR AR256150A patent/AR202848A1/es active
- 1974-10-18 JP JP49119496A patent/JPS5064299A/ja active Pending
- 1974-10-18 GB GB4523874A patent/GB1428085A/en not_active Expired
- 1974-10-21 DD DD181806A patent/DD115674A5/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES431124A1 (es) | 1976-11-01 |
| SE7413067L (xx) | 1975-04-21 |
| DE2447776A1 (de) | 1975-04-24 |
| ZA745987B (en) | 1975-09-24 |
| IE39948L (en) | 1975-04-19 |
| AR202848A1 (es) | 1975-07-24 |
| FR2250757A1 (xx) | 1975-06-06 |
| IE39948B1 (en) | 1979-01-31 |
| US3864328A (en) | 1975-02-04 |
| FI296574A (xx) | 1975-04-20 |
| DD115674A5 (xx) | 1975-10-12 |
| LU71132A1 (xx) | 1976-08-19 |
| NL7413535A (nl) | 1975-04-22 |
| BE821221A (fr) | 1975-04-18 |
| IL45863A0 (en) | 1974-12-31 |
| FR2250757B1 (xx) | 1976-10-22 |
| DK521074A (xx) | 1975-06-16 |
| JPS5064299A (xx) | 1975-05-31 |
| AU7449174A (en) | 1976-04-29 |
| GB1428085A (en) | 1976-03-17 |
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