JP2013528200A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013528200A5 JP2013528200A5 JP2013513736A JP2013513736A JP2013528200A5 JP 2013528200 A5 JP2013528200 A5 JP 2013528200A5 JP 2013513736 A JP2013513736 A JP 2013513736A JP 2013513736 A JP2013513736 A JP 2013513736A JP 2013528200 A5 JP2013528200 A5 JP 2013528200A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- iii
- amine
- diester
- 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.)
- Ceased
Links
- -1 ester amide compound Chemical class 0.000 claims 23
- 150000001412 amines Chemical class 0.000 claims 16
- 238000000034 method Methods 0.000 claims 12
- 150000007514 bases Chemical class 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000003960 organic solvent Substances 0.000 claims 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- 125000006219 1-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000004337 3-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000003469 3-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005917 3-methylpentyl group Chemical group 0.000 claims 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- GHVZOJONCUEWAV-UHFFFAOYSA-N [K].CCO Chemical compound [K].CCO GHVZOJONCUEWAV-UHFFFAOYSA-N 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 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 claims 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 claims 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1054534A FR2961205B1 (fr) | 2010-06-09 | 2010-06-09 | Procede de preparation de composes esteramides |
| FR1054534 | 2010-06-09 | ||
| PCT/FR2011/051315 WO2011154661A1 (fr) | 2010-06-09 | 2011-06-09 | Procede de preparation de composes esteramides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013528200A JP2013528200A (ja) | 2013-07-08 |
| JP2013528200A5 true JP2013528200A5 (enExample) | 2014-07-24 |
Family
ID=42751873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013513736A Ceased JP2013528200A (ja) | 2010-06-09 | 2011-06-09 | エステルアミド化合物を調製する方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9284262B2 (enExample) |
| EP (1) | EP2580186B1 (enExample) |
| JP (1) | JP2013528200A (enExample) |
| CN (1) | CN103201256B (enExample) |
| BR (1) | BR112012031314A2 (enExample) |
| FR (1) | FR2961205B1 (enExample) |
| WO (1) | WO2011154661A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2957596B1 (fr) * | 2010-03-18 | 2013-07-12 | Rhodia Operations | Nouveaux composes de type esteramide, leurs procedes de preparation et leurs utilisations |
| FR2961206B1 (fr) * | 2010-06-09 | 2012-07-20 | Rhodia Operations | Procede de preparation de composes esteramides |
| KR20150041017A (ko) | 2012-08-06 | 2015-04-15 | 솔베이 스페셜티 폴리머스 이태리 에스.피.에이. | 혼성 플루오로중합체 조성물 |
| JP6309537B2 (ja) | 2012-12-19 | 2018-04-11 | ソルヴェイ（ソシエテ アノニム） | スルホンポリマー膜の製造方法 |
| PL3110859T3 (pl) | 2014-02-28 | 2020-12-14 | Solvay Specialty Polymers Italy S.P.A. | Sieciowalne fluoropolimery |
| US20170137658A1 (en) | 2014-05-09 | 2017-05-18 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer compositions |
| WO2015193321A1 (en) | 2014-06-19 | 2015-12-23 | Solvay Specialty Polymers Italy S.P.A. | Fluoropolymer composition |
| FR3041357B1 (fr) * | 2015-09-17 | 2017-09-01 | Rhodia Operations | Solvants de decapage des resines photosensibles |
| KR102585629B1 (ko) | 2015-12-16 | 2023-10-06 | 솔베이 스페셜티 폴리머스 이태리 에스.피.에이. | 다층 조립체 |
| WO2019096800A1 (en) | 2017-11-14 | 2019-05-23 | Solvay Specialty Polymers Italy S.P.A. | Multilayer assembly |
| CN111393886B (zh) * | 2020-05-14 | 2022-08-26 | 黄山华惠科技有限公司 | 一种羟烷基酰胺固化剂及其制备方法、应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3288794A (en) | 1962-09-12 | 1966-11-29 | C P Hall Company Of Illinois | Method of making amides of dimethylamine and piperazine |
| US3417114A (en) * | 1965-07-20 | 1968-12-17 | C P Hall Company Of Illinois | Method of making amides from moisture and acid-gas containing esters |
| EP0143303A3 (de) | 1983-10-29 | 1986-04-30 | Bayer Ag | Verfahren zur Herstellung von substituierten Bernsteinsäureamiden |
| EP0445096A1 (en) * | 1990-02-26 | 1991-09-04 | Monsanto Company | Process for preparing metal-free fatty peroxyacid precusors having amide moieties in the fatty chain |
| US5325093A (en) * | 1991-05-08 | 1994-06-28 | Sony Corporation | Analog-to-digital converter for composite video signals |
| US5166407A (en) * | 1992-01-27 | 1992-11-24 | Monsanto Company | Process for preparing fatty peroxyacid precursors having amide moieties in the fatty chain |
| CN101098851B (zh) * | 2005-01-13 | 2011-02-23 | 出光兴产株式会社 | β-烷氧基丙酰胺类、溶剂、洗涤剂和液态药物组合物以及β-烷氧基丙酰胺类的制备方法 |
| CN101945575B (zh) * | 2008-01-25 | 2014-11-19 | 罗地亚管理公司 | 酯酰胺的用途、新的酯酰胺以及酯酰胺的制备方法 |
| FR2961206B1 (fr) * | 2010-06-09 | 2012-07-20 | Rhodia Operations | Procede de preparation de composes esteramides |
-
2010
- 2010-06-09 FR FR1054534A patent/FR2961205B1/fr not_active Expired - Fee Related
-
2011
- 2011-06-09 EP EP11734161.0A patent/EP2580186B1/fr active Active
- 2011-06-09 US US13/702,470 patent/US9284262B2/en active Active
- 2011-06-09 BR BR112012031314A patent/BR112012031314A2/pt not_active Application Discontinuation
- 2011-06-09 WO PCT/FR2011/051315 patent/WO2011154661A1/fr not_active Ceased
- 2011-06-09 CN CN201180031774.5A patent/CN103201256B/zh active Active
- 2011-06-09 JP JP2013513736A patent/JP2013528200A/ja not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013528200A5 (enExample) | ||
| RU2009105669A (ru) | Способ получения 3-замещенных 2-амино-5-галогенбензамидов | |
| RU2012138259A (ru) | Способ получения ривароксабана | |
| CY1113812T1 (el) | Ετεροκυκλικη ενωση και φαρμακευτικη συνθεση αυτης | |
| WO2009156861A3 (en) | Substituted pyrimidone derivatives | |
| UA109883C2 (uk) | Спосіб отримання сполук для застосування як інгібіторів sglt2 | |
| RU2015103515A (ru) | Производное соединение сложного эфира 2-аминоникотиновой кислоты и бактерицид, содержащий то же самое в качестве активного ингредиента | |
| UA101482C2 (ru) | Способ получения 2'-дезокси-5-азацитидина (децитабина) | |
| JP2013528200A (ja) | エステルアミド化合物を調製する方法 | |
| RU2014103806A (ru) | Способы и промежуточные соединения для получения азаиндолов | |
| AR064760A1 (es) | Derivados de diazol como inhibidores de la eg-5 | |
| PE20100487A1 (es) | Nuevo procedimiento de sintesis de la ivabradina y de sus sales de adicion a un acido farmaceuticamente aceptable | |
| EP3514142B1 (en) | Sulfuric acid ester or salt thereof, and surfactant | |
| RU2011140724A (ru) | Способ модификации гиалуроновой кислоты с помощью комплекса (о-ацил-о'-алкилкарбонат - замещенный пиридин) | |
| MX2013000288A (es) | Metodo para fabricar quinolina-3-carboxamidas. | |
| RU2012122367A (ru) | Способ получения простагландинов и промежуточные соединения для их получения | |
| AR051373A1 (es) | Procedimiento para la preparacion de analogos aciclicos de nucleotidos de fosfonatos | |
| CO6341560A2 (es) | Proceso para la preparacion de derivados de pirimidina sustituidos. | |
| RU2012142223A (ru) | Пространственно-затрудненные амины | |
| JP2013531640A5 (enExample) | ||
| RU2015108907A (ru) | Способы и фармацевтические композиции для лечения синдрома дауна | |
| MX2009011607A (es) | Alquiloxi-eteres novedosos y alcoxilatos de los mismos. | |
| MX2013008595A (es) | Procedimiento mejorado para la preparacion de 2,2-difluoroetilamina. | |
| RU2013110311A (ru) | Синтез соединений тиазолидиндиона | |
| MY160912A (en) | Formulations |