SU474138A3 - Способ получени замещенных норациметадолкарбамата - Google Patents
Способ получени замещенных норациметадолкарбаматаInfo
- Publication number
- SU474138A3 SU474138A3 SU1878951A SU1878951A SU474138A3 SU 474138 A3 SU474138 A3 SU 474138A3 SU 1878951 A SU1878951 A SU 1878951A SU 1878951 A SU1878951 A SU 1878951A SU 474138 A3 SU474138 A3 SU 474138A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- methyl
- obtaining
- noraciomedolcarbamate
- substituted
- acetoxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- -1 N-methyl-N- (1-methyl-3,3-diphenyl-4-acetoxy-n-hexyl) -carbamic acid Chemical compound 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 241000442132 Lactarius lactarius Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 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
- 238000005636 thioacylation reaction Methods 0.000 description 1
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22069872A | 1972-01-25 | 1972-01-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU474138A3 true SU474138A3 (ru) | 1975-06-14 |
Family
ID=22824588
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1878951A SU474138A3 (ru) | 1972-01-25 | 1973-01-24 | Способ получени замещенных норациметадолкарбамата |
Country Status (22)
-
0
- BE BE794390D patent/BE794390A/xx unknown
-
1972
- 1972-01-25 ES ES410947A patent/ES410947A1/es not_active Expired
- 1972-01-25 US US00220698A patent/US3755416A/en not_active Expired - Lifetime
-
1973
- 1973-01-16 ZA ZA730327A patent/ZA73327B/xx unknown
- 1973-01-17 IL IL41308A patent/IL41308A/xx unknown
- 1973-01-18 AU AU51225/73A patent/AU472051B2/en not_active Expired
- 1973-01-19 PH PH14262*UA patent/PH9470A/en unknown
- 1973-01-22 GB GB309173A patent/GB1374943A/en not_active Expired
- 1973-01-22 SE SE7300839A patent/SE376414B/xx unknown
- 1973-01-22 DE DE2303021A patent/DE2303021A1/de active Pending
- 1973-01-23 IE IE104/73A patent/IE37137B1/xx unknown
- 1973-01-24 DD DD168422A patent/DD103892A5/xx unknown
- 1973-01-24 CH CH98773A patent/CH554847A/fr not_active IP Right Cessation
- 1973-01-24 AT AT57873A patent/AT320663B/de not_active IP Right Cessation
- 1973-01-24 FR FR7302473A patent/FR2181688B1/fr not_active Expired
- 1973-01-24 HU HUEI458A patent/HU166566B/hu unknown
- 1973-01-24 SU SU1878951A patent/SU474138A3/ru active
- 1973-01-25 JP JP48010624A patent/JPS4881840A/ja active Pending
- 1973-01-25 NL NL7301122A patent/NL7301122A/xx unknown
- 1973-01-25 CS CS579A patent/CS164223B2/cs unknown
- 1973-01-25 RO RO7300073606A patent/RO62268A/ro unknown
- 1973-01-25 AR AR246281A patent/AR196511A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| AT320663B (de) | 1975-02-25 |
| CH554847A (fr) | 1974-10-15 |
| FR2181688B1 (enrdf_load_stackoverflow) | 1976-07-02 |
| IE37137L (en) | 1973-07-25 |
| NL7301122A (enrdf_load_stackoverflow) | 1973-07-27 |
| AR196511A1 (es) | 1974-02-06 |
| IL41308A0 (en) | 1973-03-30 |
| PH9470A (en) | 1975-12-16 |
| AU5122573A (en) | 1974-07-18 |
| ES410947A1 (es) | 1976-05-16 |
| ZA73327B (en) | 1974-08-28 |
| SE376414B (enrdf_load_stackoverflow) | 1975-05-26 |
| JPS4881840A (enrdf_load_stackoverflow) | 1973-11-01 |
| AU472051B2 (en) | 1976-05-13 |
| GB1374943A (en) | 1974-11-20 |
| CS164223B2 (enrdf_load_stackoverflow) | 1975-11-07 |
| BE794390A (fr) | 1973-07-23 |
| FR2181688A1 (enrdf_load_stackoverflow) | 1973-12-07 |
| DD103892A5 (enrdf_load_stackoverflow) | 1974-02-12 |
| US3755416A (en) | 1973-08-28 |
| DE2303021A1 (de) | 1973-08-09 |
| IL41308A (en) | 1975-04-25 |
| RO62268A (fr) | 1977-10-15 |
| IE37137B1 (en) | 1977-05-11 |
| HU166566B (enrdf_load_stackoverflow) | 1975-04-28 |
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