ZA200006713B - Improved process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives. - Google Patents
Improved process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives. Download PDFInfo
- Publication number
- ZA200006713B ZA200006713B ZA200006713A ZA200006713A ZA200006713B ZA 200006713 B ZA200006713 B ZA 200006713B ZA 200006713 A ZA200006713 A ZA 200006713A ZA 200006713 A ZA200006713 A ZA 200006713A ZA 200006713 B ZA200006713 B ZA 200006713B
- Authority
- ZA
- South Africa
- Prior art keywords
- formula
- process according
- compound
- manufacture
- toluene
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 81
- 150000001875 compounds Chemical class 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- -1 amino nitrile compound Chemical class 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 5
- 150000008041 alkali metal carbonates Chemical class 0.000 claims description 5
- 150000004820 halides Chemical class 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 5
- 239000006184 cosolvent Substances 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 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 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 48
- 239000000047 product Substances 0.000 description 20
- 239000000243 solution Substances 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 238000004128 high performance liquid chromatography Methods 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical class CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- ONQSXERGNKDILF-RXMQYKEDSA-N (2r)-2-(2,4-dichlorophenoxy)propanoyl chloride Chemical compound ClC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl ONQSXERGNKDILF-RXMQYKEDSA-N 0.000 description 4
- CAOHBROWLMCZRP-UHFFFAOYSA-N 2-amino-2,3-dimethylbutanenitrile Chemical compound CC(C)C(C)(N)C#N CAOHBROWLMCZRP-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 125000005219 aminonitrile group Chemical group 0.000 description 4
- 229940080818 propionamide Drugs 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000012258 stirred mixture Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 230000003032 phytopathogenic effect Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 125000005270 trialkylamine group Chemical group 0.000 description 2
- CAOHBROWLMCZRP-ZCFIWIBFSA-N (2s)-2-amino-2,3-dimethylbutanenitrile Chemical compound CC(C)[C@](C)(N)C#N CAOHBROWLMCZRP-ZCFIWIBFSA-N 0.000 description 1
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical compound OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012272 crop production Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/062,975 US5942640A (en) | 1998-04-20 | 1998-04-20 | Process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200006713B true ZA200006713B (en) | 2001-11-19 |
Family
ID=22046082
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200006713A ZA200006713B (en) | 1998-04-20 | 2000-11-17 | Improved process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5942640A (ko) |
| EP (1) | EP1071659A1 (ko) |
| JP (1) | JP2002512217A (ko) |
| KR (1) | KR20010071161A (ko) |
| CN (1) | CN1298384A (ko) |
| AR (1) | AR018190A1 (ko) |
| AU (1) | AU3382499A (ko) |
| BR (1) | BR9909759A (ko) |
| CA (1) | CA2328723A1 (ko) |
| CO (1) | CO4810332A1 (ko) |
| EA (1) | EA200001020A1 (ko) |
| HU (1) | HUP0101750A2 (ko) |
| IL (1) | IL138843A0 (ko) |
| NZ (1) | NZ507532A (ko) |
| PL (1) | PL343629A1 (ko) |
| SK (1) | SK14772000A3 (ko) |
| WO (1) | WO1999054287A1 (ko) |
| ZA (1) | ZA200006713B (ko) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1982290A (zh) * | 1997-02-04 | 2007-06-20 | 阿肯色大学评议会 | 杀菌的羧酰胺 |
| DE19947613A1 (de) * | 1998-10-07 | 2000-04-13 | Sumitomo Chemical Co | Cyanatreinigungsverfahren |
| AU2560300A (en) * | 1999-02-20 | 2000-09-04 | Astrazeneca Ab | Acetamido acetonitrile derivatives as inhibitors of cathepsin l and/or cathepsins |
| CN1512983A (zh) * | 2001-06-01 | 2004-07-14 | AXYSҩ�﹫˾ | 作为组织蛋白酶s抑制剂的化合物和组合物 |
| CN106366020B (zh) * | 2016-08-31 | 2018-12-11 | 京博农化科技股份有限公司 | 一种合成手性稻瘟酰胺的方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA992988A (en) * | 1971-06-25 | 1976-07-13 | Don R. Baker | N-(1,1 SUBSTITUTED ACETONITRILO)-.alpha.-(3,5-SUBSTITUTED PHENOXY) ALKYL AMIDES AND THEIR USE AS HERBICIDES |
| US3932168A (en) * | 1971-11-17 | 1976-01-13 | Abbott Laboratories | Substituted aryloxyacetamido nitrile derivatives as carbohydrate deposition agents |
| US4052432A (en) * | 1974-11-18 | 1977-10-04 | Stauffer Chemical Company | N-(1,1 Substituted acetonitrilo)-α-(3,5-substituted phenoxy) alkyl amides |
| US4087277A (en) * | 1976-05-20 | 1978-05-02 | Stauffer Chemical Company | N-(1,1-substituted acetonitrilo)-α-(3,5-substituted phenoxy) alkyl amides and their use as herbicides |
| AR220917A1 (es) * | 1977-10-26 | 1980-12-15 | Stauffer Chemical Co | Compuestos de n-sustituido-2-(4 sustituido-3,5-dimetilfenoxi)butiramida utiles como anublicidas y composicion que los contiene |
| FR2446812A1 (fr) * | 1979-01-16 | 1980-08-14 | Produits Ind Cie Fse | Phenoxy- et thiophenoxynitriles et leurs applications en tant qu'herbicides |
| DE3629441A1 (de) * | 1986-08-29 | 1988-03-03 | Celamerck Gmbh & Co Kg | Neue phenoxycarbonsaeurederivate, ihre herstellung und verwendung |
| JPH059165A (ja) * | 1991-02-18 | 1993-01-19 | Mitsubishi Petrochem Co Ltd | 置換フエノキシカルボン酸アミド誘導体 |
| JPH0570428A (ja) * | 1991-09-13 | 1993-03-23 | Mitsubishi Petrochem Co Ltd | 置換フエノキシカルボン酸アミド誘導体およびそれを含有する農業用殺菌剤 |
-
1998
- 1998-04-20 US US09/062,975 patent/US5942640A/en not_active Expired - Fee Related
-
1999
- 1999-04-05 JP JP2000544628A patent/JP2002512217A/ja active Pending
- 1999-04-05 WO PCT/US1999/007443 patent/WO1999054287A1/en not_active Application Discontinuation
- 1999-04-05 KR KR1020007011599A patent/KR20010071161A/ko active IP Right Grant
- 1999-04-05 AU AU33824/99A patent/AU3382499A/en not_active Abandoned
- 1999-04-05 CA CA002328723A patent/CA2328723A1/en not_active Abandoned
- 1999-04-05 SK SK1477-2000A patent/SK14772000A3/sk unknown
- 1999-04-05 HU HU0101750A patent/HUP0101750A2/hu unknown
- 1999-04-05 IL IL13884399A patent/IL138843A0/xx unknown
- 1999-04-05 EA EA200001020A patent/EA200001020A1/ru unknown
- 1999-04-05 CN CN99805292A patent/CN1298384A/zh active Pending
- 1999-04-05 EP EP99915270A patent/EP1071659A1/en not_active Withdrawn
- 1999-04-05 PL PL99343629A patent/PL343629A1/xx unknown
- 1999-04-05 NZ NZ507532A patent/NZ507532A/xx unknown
- 1999-04-05 BR BR9909759-1A patent/BR9909759A/pt not_active IP Right Cessation
- 1999-04-15 CO CO99022531A patent/CO4810332A1/es unknown
- 1999-04-19 AR ARP990101806A patent/AR018190A1/es not_active Application Discontinuation
-
2000
- 2000-11-17 ZA ZA200006713A patent/ZA200006713B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NZ507532A (en) | 2002-08-28 |
| AR018190A1 (es) | 2001-10-31 |
| CA2328723A1 (en) | 1999-10-28 |
| BR9909759A (pt) | 2000-12-19 |
| IL138843A0 (en) | 2001-10-31 |
| WO1999054287A1 (en) | 1999-10-28 |
| JP2002512217A (ja) | 2002-04-23 |
| US5942640A (en) | 1999-08-24 |
| EP1071659A1 (en) | 2001-01-31 |
| CN1298384A (zh) | 2001-06-06 |
| AU3382499A (en) | 1999-11-08 |
| KR20010071161A (ko) | 2001-07-28 |
| HUP0101750A2 (hu) | 2001-10-28 |
| EA200001020A1 (ru) | 2001-06-25 |
| PL343629A1 (en) | 2001-08-27 |
| SK14772000A3 (sk) | 2002-05-09 |
| CO4810332A1 (es) | 1999-06-30 |
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