SU293341A1 - - Google Patents
Info
- Publication number
- SU293341A1 SU293341A1 SU1190702A SU1190702A SU293341A1 SU 293341 A1 SU293341 A1 SU 293341A1 SU 1190702 A SU1190702 A SU 1190702A SU 1190702 A SU1190702 A SU 1190702A SU 293341 A1 SU293341 A1 SU 293341A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ethyl
- alkyl
- carbon atoms
- benzenesulfonyl
- methoxy
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- -1 methoxyethyl Chemical group 0.000 description 9
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 2
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000007659 semicarbazones Chemical class 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- MMCNDPVHBALJKB-UHFFFAOYSA-N COC(C=CC(Cl)=C1)=C1C(NCCC(C=C1)=CC=C1S(NC(N)=O)(=O)=O)=S Chemical compound COC(C=CC(Cl)=C1)=C1C(NCCC(C=C1)=CC=C1S(NC(N)=O)(=O)=O)=S MMCNDPVHBALJKB-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- VNMLVHLVBFHHSN-UHFFFAOYSA-N thiophen-2-ylcarbamic acid Chemical class OC(=O)NC1=CC=CS1 VNMLVHLVBFHHSN-UHFFFAOYSA-N 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0050451 | 1966-10-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU293341A1 true SU293341A1 (enrdf_load_stackoverflow) | |
| SU366604A3 SU366604A3 (enrdf_load_stackoverflow) | 1973-01-16 |
Family
ID=7103809
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1449348A SU415868A3 (ru) | 1966-10-15 | 1967-10-14 | Способ получения бензолсульфонилмочевины |
| SU1190702A SU366604A3 (enrdf_load_stackoverflow) | 1966-10-15 | 1967-10-14 | |
| SU1701160A SU461493A3 (ru) | 1966-10-15 | 1967-10-14 | Способ получени замещенной бензолсульфонилмочевины |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1449348A SU415868A3 (ru) | 1966-10-15 | 1967-10-14 | Способ получения бензолсульфонилмочевины |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1701160A SU461493A3 (ru) | 1966-10-15 | 1967-10-14 | Способ получени замещенной бензолсульфонилмочевины |
Country Status (24)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE755682A (fr) * | 1969-09-04 | 1971-03-03 | Geigy Ag J R | P-aminoalkyl-benzene-sulfonamides et medicaments contenant de tels composes |
| JPS543827U (enrdf_load_stackoverflow) * | 1977-06-10 | 1979-01-11 |
-
1966
- 1966-10-15 DE DE1568606A patent/DE1568606C3/de not_active Expired
-
1967
- 1967-10-02 PL PL1967122840A patent/PL71141B1/pl unknown
- 1967-10-09 IS IS1694A patent/IS752B6/is unknown
- 1967-10-09 DK DK502067AA patent/DK124401B/da not_active IP Right Cessation
- 1967-10-10 IL IL28743A patent/IL28743A/en unknown
- 1967-10-11 ES ES345990A patent/ES345990A1/es not_active Expired
- 1967-10-12 SE SE13943/67A patent/SE357558B/xx unknown
- 1967-10-12 FI FI672743A patent/FI46156C/fi active
- 1967-10-12 YU YU1984/67A patent/YU34033B/xx unknown
- 1967-10-12 MC MC722A patent/MC682A1/xx unknown
- 1967-10-12 LU LU54659D patent/LU54659A1/xx unknown
- 1967-10-13 CH CH1432767A patent/CH504418A/de not_active IP Right Cessation
- 1967-10-13 GB GB46808/67A patent/GB1185090A/en not_active Expired
- 1967-10-13 AT AT392773*1A patent/AT322569B/de not_active IP Right Cessation
- 1967-10-13 AT AT392873A patent/AT323754B/de not_active IP Right Cessation
- 1967-10-13 FR FR1570447D patent/FR1570447A/fr not_active Expired
- 1967-10-13 NO NO170120A patent/NO122415B/no unknown
- 1967-10-13 AT AT325574*1A patent/AT323193B/de not_active IP Right Cessation
- 1967-10-13 NL NL6713927.A patent/NL157896B/xx not_active IP Right Cessation
- 1967-10-13 AT AT928367A patent/AT322567B/de not_active IP Right Cessation
- 1967-10-13 AT AT392673A patent/AT323753B/de not_active IP Right Cessation
- 1967-10-14 SU SU1449348A patent/SU415868A3/ru active
- 1967-10-14 OA OA53078A patent/OA03380A/xx unknown
- 1967-10-14 SU SU1190702A patent/SU366604A3/ru active
- 1967-10-14 CU CU33282A patent/CU33282A/es unknown
- 1967-10-14 SU SU1701160A patent/SU461493A3/ru active
- 1967-10-16 JP JP42066511A patent/JPS52943B1/ja active Pending
- 1967-10-16 BE BE705156D patent/BE705156A/xx not_active IP Right Cessation
-
1968
- 1968-01-12 FR FR135759A patent/FR7215M/fr not_active Expired
- 1968-11-26 ES ES360718A patent/ES360718A1/es not_active Expired
- 1968-11-26 ES ES360714A patent/ES360714A1/es not_active Expired
- 1968-11-26 ES ES360712A patent/ES360712A1/es not_active Expired
- 1968-11-26 ES ES360715A patent/ES360715A1/es not_active Expired
- 1968-11-26 ES ES360713A patent/ES360713A1/es not_active Expired
- 1968-11-26 ES ES360716A patent/ES360716A1/es not_active Expired
- 1968-11-26 ES ES360717A patent/ES360717A1/es not_active Expired
-
1970
- 1970-11-26 CY CY56870A patent/CY568A/xx unknown
-
1971
- 1971-12-31 MY MY197153A patent/MY7100053A/xx unknown
-
1973
- 1973-04-09 YU YU949/73A patent/YU34032B/xx unknown
- 1973-04-09 YU YU951/73A patent/YU34035B/xx unknown
- 1973-04-09 YU YU950/73A patent/YU34034B/xx unknown
- 1973-04-09 YU YU948/73A patent/YU34285B/xx unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2441498A (en) | Alkyl glycinanilides | |
| JP2515427B2 (ja) | プレウロムチリン類 | |
| US2375138A (en) | Alkamine esters of aryloxymethyl benzoic acid | |
| EP4284778A1 (en) | Method for preparing levetiracetam and intermediates thereof | |
| SU293341A1 (enrdf_load_stackoverflow) | ||
| US2467371A (en) | Biguanide derivatives | |
| SU664561A3 (ru) | Способ получени производных 2-/4(ациламиноалкил)-фенокси/-алкилкарбоновой кислоты или их солей | |
| US3168531A (en) | 1-aryl-5-(p-lower alkoxyphenyl)-pyrrole-2-propionic acid compounds | |
| JPS5829287B2 (ja) | Ｎ−置換アクリルアミドまたはｎ−置換メタクリルアミドの製造方法 | |
| RU2106339C1 (ru) | Циклогексанолнитраты, способ их получения и лекарственное средство | |
| JPS5922711B2 (ja) | ベンゾオキサゾリノン誘導体の製造法 | |
| JPS6178778A (ja) | ４，５‐ジヒドロ‐４‐オキソ‐２‐〔（２‐ｔｒａｎｓ‐フエニルシクロプロピル）アミノ〕‐３‐フランカルボン酸とその誘導体 | |
| JP2668816B2 (ja) | ベンゾチアジアゾール誘導体の製法 | |
| US3188312A (en) | New process for the preparation of thiourea derivatives | |
| US4007203A (en) | 4-(1-Pyrolidenyl)-2H-1-benzothiopyran-3-carboxanilide | |
| US4486597A (en) | Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives | |
| US4587356A (en) | Process for the production of nuclear substituted cinnamoylanthranilic acid derivatives | |
| CN102596915B (zh) | 2-硫代组氨酸及类似物的合成方法 | |
| CN1243738C (zh) | 一种1－炔丙基海因的制备方法 | |
| JPH02273677A (ja) | ２―フェニルベンゾトリアゾール類の製造法 | |
| JPS63233962A (ja) | 新規アミノ‐プロパノール誘導体、その製法及びこれを含有する心臓‐及び循環系疾患‐治療剤、中間体及びその製法 | |
| US3103520A (en) | Aminobenzoxacycloalkanes | |
| SU212856A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ а- | |
| SU341227A1 (enrdf_load_stackoverflow) | ||
| CA2154558C (en) | Process for preparing c-substituted diethylene triamines |