GB1000192A - - Google Patents
Info
- Publication number
- GB1000192A GB1000192A GB1000192DA GB1000192A GB 1000192 A GB1000192 A GB 1000192A GB 1000192D A GB1000192D A GB 1000192DA GB 1000192 A GB1000192 A GB 1000192A
- Authority
- GB
- United Kingdom
- Prior art keywords
- iminodibenzyl
- methyl
- compound
- group
- alkyl
- 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.)
- Active
Links
- -1 iminodibenzyl compounds Chemical class 0.000 abstract 12
- 150000001875 compounds Chemical class 0.000 abstract 6
- ZSMRRZONCYIFNB-UHFFFAOYSA-N 6,11-dihydro-5h-benzo[b][1]benzazepine Chemical class C1CC2=CC=CC=C2NC2=CC=CC=C12 ZSMRRZONCYIFNB-UHFFFAOYSA-N 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- 239000007858 starting material Substances 0.000 abstract 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 231100000252 nontoxic Toxicity 0.000 abstract 2
- 230000003000 nontoxic effect Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- NYYRRBOMNHUCLB-UHFFFAOYSA-N 3-chloro-n,n-dimethylpropan-1-amine Chemical compound CN(C)CCCCl NYYRRBOMNHUCLB-UHFFFAOYSA-N 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000005277 alkyl imino group Chemical group 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 229940124326 anaesthetic agent Drugs 0.000 abstract 1
- 230000003444 anaesthetic effect Effects 0.000 abstract 1
- 230000003266 anti-allergic effect Effects 0.000 abstract 1
- 230000003474 anti-emetic effect Effects 0.000 abstract 1
- 239000002111 antiemetic agent Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical group C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 1
- YXHMPUVTZRRMNB-UHFFFAOYSA-N ethyl n-(3-chloropropyl)-n-methylcarbamate Chemical compound CCOC(=O)N(C)CCCCl YXHMPUVTZRRMNB-UHFFFAOYSA-N 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 150000003141 primary amines Chemical class 0.000 abstract 1
- 230000001624 sedative effect Effects 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1000192A true GB1000192A (enrdf_load_stackoverflow) |
Family
ID=1754830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1000192D Active GB1000192A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1000192A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3931151A (en) * | 1972-10-09 | 1976-01-06 | Roussel-Uclaf | Dibenzo (b,f) azepines |
-
0
- GB GB1000192D patent/GB1000192A/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3931151A (en) * | 1972-10-09 | 1976-01-06 | Roussel-Uclaf | Dibenzo (b,f) azepines |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2750387A (en) | Basically substituted derivatives of diarylaminobenzamides | |
| US3388128A (en) | Substituted 1, 4-diazabicyclo [4. 4. 9] decanes | |
| CN114195730A (zh) | 一种苯并[e][1,3]噁嗪-2,4-二酮的制备方法 | |
| FI954067A0 (fi) | Menetelmä valmistaa bentsoehappojohdannaisia välituotteina ja bentsotiofeeneja farmaseuttisina aineina | |
| US4101661A (en) | Novel antibacterial amide compounds and process means for producing the same | |
| GB1000192A (enrdf_load_stackoverflow) | ||
| NO158687B (no) | Diafragmadukovertrukket elektroderamme for elektrolytisk utvinning eller raffinering av metaller. | |
| US3311636A (en) | Organic chemical compounds and process | |
| EP0272462B1 (en) | Process for preparing ursodeoxycholic acid derivates and their inorganic and organic salts having therpeutic activity. | |
| NO992058L (no) | FremgangsmÕte for fremstilling av fysostigminkarbamatderivater fra eseretoler | |
| NO742246L (enrdf_load_stackoverflow) | ||
| US3959298A (en) | Process for preparing triacetonamine | |
| US2642433A (en) | Alpha-amino-alpha, alpha-diphenylacetic acid derivatives and method of preparing same | |
| US3970661A (en) | 2-Amino, 5-carbamoyl pyridine compounds | |
| US3717637A (en) | TRIFLUOROMETHYLTHIO SUBSTITUTED DIBENZ [b,f] [1,4] OXAZEPINES | |
| US3342807A (en) | Iminodibenzyl derivatives | |
| US3719668A (en) | Semi-synthetic penicillin esters | |
| NO792590L (no) | Alfa-aminofenyleddiksyrederivater. | |
| EP1533314A1 (en) | Process for producing cyclic thioether and synthetic intermediate thereof | |
| US3712889A (en) | Oxodihydrobenzothiazine-s-dioxides | |
| US3970663A (en) | Certain amino-nicotinamide derivatives | |
| US3498978A (en) | 3-pipecoline derivatives | |
| US3192197A (en) | 3-(substituted) sulphonyl-5-alkanoyliminodibenzyls useful in the preparation of derivatives of dibenz [b, f] azepines | |
| US20040058979A1 (en) | Indoline derivative and process for producing the same | |
| ES2214506T3 (es) | Procedimientos y compuestos intermedios para la preparacion de 5,7-dihidro-3-(2-(1-bencilpiperidin-4-il)etil)-6h-pirrolo-(4,5-f)-1,2-bencisoxazol-6-ona. |