WO1990012002A1 - Preparation of substituted ethenes - Google Patents
Preparation of substituted ethenes Download PDFInfo
- Publication number
- WO1990012002A1 WO1990012002A1 PCT/GB1990/000501 GB9000501W WO9012002A1 WO 1990012002 A1 WO1990012002 A1 WO 1990012002A1 GB 9000501 W GB9000501 W GB 9000501W WO 9012002 A1 WO9012002 A1 WO 9012002A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- salt
- amine
- reaction
- product
- dipotassium
- Prior art date
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- 238000002360 preparation method Methods 0.000 title description 4
- 238000006243 chemical reaction Methods 0.000 claims abstract description 32
- 150000001412 amines Chemical class 0.000 claims abstract description 21
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 13
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 11
- -1 heterocyclic alkylamines Chemical group 0.000 claims abstract description 11
- 150000003973 alkyl amines Chemical class 0.000 claims abstract description 10
- ULOTWPOKIYOEQN-UHFFFAOYSA-N 2-nitroethanedithioic acid Chemical compound [O-][N+](=O)CC(S)=S ULOTWPOKIYOEQN-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 9
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims abstract description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000003975 aryl alkyl amines Chemical group 0.000 claims abstract description 8
- ZILSBZLQGRBMOR-UHFFFAOYSA-N 1,3-benzodioxol-5-ylmethanamine Chemical compound NCC1=CC=C2OCOC2=C1 ZILSBZLQGRBMOR-UHFFFAOYSA-N 0.000 claims abstract description 7
- DXSUORGKJZADET-UHFFFAOYSA-N 3,3-dimethylbutan-2-amine Chemical compound CC(N)C(C)(C)C DXSUORGKJZADET-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 34
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 230000002152 alkylating effect Effects 0.000 claims description 7
- HRCSDUZVYNAMRQ-UHFFFAOYSA-L dipotassium;2-nitroethanedithioate Chemical compound [K+].[K+].[O-][N+](=O)CC([S-])=S.[O-][N+](=O)CC([S-])=S HRCSDUZVYNAMRQ-UHFFFAOYSA-L 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- ZVIREQPONFZPLQ-UHFFFAOYSA-N 1-nitroethenamine Chemical compound NC(=C)[N+]([O-])=O ZVIREQPONFZPLQ-UHFFFAOYSA-N 0.000 claims description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 4
- 230000029936 alkylation Effects 0.000 claims description 4
- 238000005804 alkylation reaction Methods 0.000 claims description 4
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims description 4
- HXRSXEDVVARPHP-UDWIEESQSA-N (z)-1-n'-(1,3-benzodioxol-5-ylmethyl)-1-n-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-2-nitroethene-1,1-diamine Chemical compound O1C(CN(C)C)=CC=C1CSCCN\C(=C/[N+]([O-])=O)NCC1=CC=C(OCO2)C2=C1 HXRSXEDVVARPHP-UDWIEESQSA-N 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 229960001323 niperotidine Drugs 0.000 claims description 3
- 150000003141 primary amines Chemical class 0.000 claims description 3
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 claims description 2
- 229940073608 benzyl chloride Drugs 0.000 claims description 2
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 claims description 2
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims description 2
- 229940102396 methyl bromide Drugs 0.000 claims description 2
- 239000012022 methylating agents Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- 239000002609 medium Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- VNQGHTYUUFTLBB-UHFFFAOYSA-N 3,3-dimethyl-n-(1-methylsulfanyl-2-nitroethenyl)butan-2-amine Chemical compound [O-][N+](=O)C=C(SC)NC(C)C(C)(C)C VNQGHTYUUFTLBB-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- 238000006254 arylation reaction Methods 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000011877 solvent mixture Substances 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 abstract 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 11
- 238000005576 amination reaction Methods 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000011987 methylation Effects 0.000 description 2
- 238000007069 methylation reaction Methods 0.000 description 2
- HUDRYGJMGVJMCD-UHFFFAOYSA-N n,n-dimethyl-1-methylsulfanyl-2-nitroethenamine Chemical compound CSC(N(C)C)=C[N+]([O-])=O HUDRYGJMGVJMCD-UHFFFAOYSA-N 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- MAUMSNABMVEOGP-UHFFFAOYSA-N (methyl-$l^{2}-azanyl)methane Chemical compound C[N]C MAUMSNABMVEOGP-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- GTXHAUIBAMKCAF-UHFFFAOYSA-N 1-methylsulfanyl-2-nitro-3-phenylprop-1-en-1-amine Chemical compound CSC(N)=C([N+]([O-])=O)CC1=CC=CC=C1 GTXHAUIBAMKCAF-UHFFFAOYSA-N 0.000 description 1
- DZDKFYMSTBDSGF-UHFFFAOYSA-N 1-methylsulfanyl-2-nitroethenamine Chemical compound CSC(N)=C[N+]([O-])=O DZDKFYMSTBDSGF-UHFFFAOYSA-N 0.000 description 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- YDFYTQPYSUXHID-UHFFFAOYSA-N [O-][N+](=O)CC(S)=S.[O-][N+](=O)C=C(S)S Chemical compound [O-][N+](=O)CC(S)=S.[O-][N+](=O)C=C(S)S YDFYTQPYSUXHID-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 125000004948 alkyl aryl alkyl group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 229960004979 fampridine Drugs 0.000 description 1
- 125000005241 heteroarylamino group Chemical group 0.000 description 1
- 239000003485 histamine H2 receptor antagonist Substances 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- YQFHPXZGXNYYLD-UHFFFAOYSA-N n-methyl-1-methylsulfanyl-2-nitroethenamine Chemical compound CNC(SC)=C[N+]([O-])=O YQFHPXZGXNYYLD-UHFFFAOYSA-N 0.000 description 1
- 150000008320 nitroethenes Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/22—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/27—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and unsaturated
Definitions
- the present invention relates to certain substituted ethenes, specifically certain N-substituted alkyl or
- Spanish Patent Specification No. 523448 describes the preparation of N-methyl-1-methylthio-2-nitroethenamine from tne dipotassium salt of 2-nitrodithioacetic acid (1-nitro-2,2- bismercapto-ethylene) by a three stage process involving firstly the methylation of one only of the KS-groups by reaction with dimethyl sulphate, secondly the conversion of the resulting CH 3 S-group into a CH 3 NH- group by reaction
- the present invention provides a method for the
- alkylamines are not straight chain primary amines containing a heteroatom in the chain, with the dipotassium salt of a 2- nitrodithioaliphatic acid.
- This process is robust in that it does not require close control at each process step, does not oversubstitute at all during the amination to give the bisaminated derivative and can give an excellent yield.
- the monopotassium salt so obtained may be alkylated or arylalkylated to give the required alkyl or arylalkyl thionitroethenamine.
- dipotassium salt namely Gipotassium 2-nitrodithioacetate (a l so known as dipotassium nitrothiolothionoacetate), and an amine, such as
- This intermediate may then be converted to N,N-dimethyl-1- methylthio-2-nitroethenamine by reaction with a methylating agent, such as dimethyl sulphate, as follows:
- amines the use of which is within the scope of the present invention may be selected from other secondary aliphatic amines, substituted or branched chain aliphatic amines, for example pinacolyl amine ( 3-amino-2,2-dimethyl- butane), arylalkylamines, for example benzylamine
- heterocyclic alkylamines for example piperonylamine (3,4-methylene-dioxybenzylamine or
- the dipotassium salt of 2-nitrodithioacetic acid required as a starting material may be prepared by the method of E Freund, Chem. Ber. 52 , 542 (1919) which produces an ethanol-wet cake. Weights given herein are on a 100% basis, the ethanol being treated as solvent. Analogues of the dipotassium salt of 2-nitrodithioacetic acid, such as those based on butene and propene, can be made by analogous methods.
- reaction I we prefer to carry out the amination reaction (Reaction I) in a polar solvent, for example, water, methanol, ethanol, isopropanol or dimethyl sulphoxide. On costs and ease of handling, water is the preferred solvent.
- a polar solvent for example, water, methanol, ethanol, isopropanol or dimethyl sulphoxide.
- water is the preferred solvent.
- the reaction concentration water or other solvent to
- dipotassium salt of nitrodithioacetic acid can be 20:1 to 1:1, but. is preferably 10:1 to 5:1 by weight.
- nitrodithioacetic acid as prepared is included as solvent in the above ranges of concentrations and reference to an aqueous solvent includes such minor contents of polar organic solvents. All concentrations quoted herein are in parts by weight unless otherwise stated.
- the reaction temperature for the amination reaction can be in the range 0°C to 100°C but it is preferably between 20°C and 60°C.
- the amination product may be used as a solution as formed or may be recovered.
- the alkylation or arylalky lation reaction to convert the thioamide salt to the thio-alkyl derivative (Reaction II) can be carried out in the range 0°C to 60°C, but it is preferably carried out in the range 10°C to 40°C so as to give an acceptable reaction time and avoid side reactions.
- Suitable alkylating or arylalkylating agents are alkyl halides or sulphates and the benzyl halides. Particularly convenient agents are dimethyl sulphate, diethyl sulphate, methyl chloride, methyl bromide, methyl iodide and benzyl chloride. Conveniently the alkylation or ary lalkylation is effected in the presence of a phase transfer agent such as benzy Itrimethylammonium chloride.
- molar ratios of alkylating/arylalkylating agent : dipotassium salt of nitrodithioacetic acid of 1:1 to >4:1 can be used, but optimum yields are obtained using a molar ratio of 2:1 to 2.5: 1.
- the product nitroethenamine may be recovered by
- a suitable organic solvent which is, preferably, a water immiscible chlorinated solvent such as m ⁇ thylene chloride, ethylene dichloride or
- chlcrcbenzene This may be followed by drying, concentrating and recrystal lising from a suitable solvent such as propan- 2-ol.
- X represents an alkyl arylalkyl or heterocyclicalky 1 group.
- the dipotassium salt is dipotassium nitrodithioacetate
- the amine used in Reaction I is piperonylamine and where the alkylated or arylalkylated product of Reaction II is then reacted with 2- [5-(N,N-dimethylaminomethyl)
- Reaction I and II for example where the same dipotassium salt is used and wherein the amine used in Reaction I is pinacolylamine and where the product of reaction II is reacted with a range of aryl or heteroaryl amines such as 4- aminopyridine in particular, a range of compounds having hypotensive properties may be produced.
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Luminescent Compositions (AREA)
- Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Underground Structures, Protecting, Testing And Restoring Foundations (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
Abstract
A potassium salt useful in the production of certain N-substituted alkyl or arylalkyl thionitroethenamines is produced by the reaction of the dipotassium salt of a 2-nitrodithio aliphatic acid such as 2-nitrodithio acetic acid with branched chain primary alkylamines, secondary alkylamines, arylalkylamines or heterocyclic alkylamines such as dimethylamine, pinacolylamine, benzylamine or piperonylamine, thereby converting one only of the KS-groups to an alkylamine group. The resulting monopotassium salt may be alkylated or arylalkylated to produce an N-substituted alkyl or arylalkyl thionitroethenamine. This compound may be reacted with a suitable amine to produce compounds containing the pharmaceutically active grouping -NHC(=CHNO2?)NHX, wherein X represents an alkyl, arylalkyl or heterocyclic alkyl group.
Description
Preparation of Substituted Ethenes
The present invention relates to certain substituted ethenes, specifically certain N-substituted alkyl or
arylalkyl thionitroethenamines, derivatives thereof,
intermediates in the production thereof and processes for the manufacture of all the aforesaid.
In general terms the said family of nitroethenes is known, although certain particular nitrcerhenes disclosed herein are believed to be novel, and have known uses as intermediates in the manufacture of pharmaceutical compounds such as the histamine H2 antagonists containing the
pharmaceutically active end group -NHC(=CHNO2)NHX wherein X is an organic radical, for eκamole niperotidine which has the
Spanish Patent Specification No. 523448 describes the preparation of N-methyl-1-methylthio-2-nitroethenamine from tne dipotassium salt of 2-nitrodithioacetic acid (1-nitro-2,2- bismercapto-ethylene) by a three stage process involving firstly the methylation of one only of the KS-groups by reaction with dimethyl sulphate, secondly the conversion of
the resulting CH3S-group into a CH3NH- group by reaction
with methylamine and thirdly, the methylation of the second
KS-group by reaction with a further quantity of dimethyl
sulphate. This patent is silent as to any possibility for producing other N-substituted thionitroethenamines.
The process described in the Spanish Patent requires
careful control at all stages to avoid the production of
unwanted reaction products such as the bis(methylthio)
derivative and is disadvantageous in requiring a repetition of the dimethyl sulphate reaction due to the toxic nature of that compound.
It is known in the chemical art that, in general,
amines do not react with dianions since the lone pair
electrons on the amine inhibit reaction with a molecule
which is already doubly negatively charged. This inhibition dees not apply to dimethyl sulphate. The processing
sequence of the Spanish Patent No. 523448 is therefore in
accord with current belief in the art.
The present applicant has found, however, that certain amines can be made to react directly with the 2- nitrcdithioacetate dianion. This has enabled a highly
selective two stage process for the production of
aminosubstituted thiosubstituted nitrcethenes to be
developed.
The present invention provides a method for the
production of a monopotassium salt useful in the production of N- substituted alkyl or arylalkyl thionitroethenamines
characterised by reacting an amine selected from branched
chain primary alkylamines, secondary alkylamines,
arylalkylamines and heterocyclic alkylamines, wnerein the
alkyl moieties of said arylalkylamines and heterocyclic
alkylamines are not straight chain primary amines containing a heteroatom in the chain, with the dipotassium salt of a 2- nitrodithioaliphatic acid.
This process is robust in that it does not require close control at each process step, does not oversubstitute at all during the amination to give the bisaminated derivative and
can give an excellent yield.
The monopotassium salt so obtained may be alkylated or arylalkylated to give the required alkyl or arylalkyl thionitroethenamine.
In the case of the simplest dipotassium salt, namely Gipotassium 2-nitrodithioacetate (a l so known as dipotassium nitrothiolothionoacetate), and an amine, such as
dimethylamine, the sequence of reactions outlined above is as follows: =CHNO2 + (CH3)2NH
Reaction I
(CH3)2N
C=CHNO2 KSH
K+S
This intermediate may then be converted to N,N-dimethyl-1- methylthio-2-nitroethenamine by reaction with a methylating agent, such as dimethyl sulphate, as follows:
(CH3)2SO4 Reaction II
(CH3)2
=CHNO2 + CH3SH + KCH3SO4
CH3
These reactions proceed analogously when using other
alkyl, arylalkyl or heterocyclic alkyl amines in Reaction I or other alkylating or arylalkylating agents in Reaction II.
Other amines the use of which is within the scope of the present invention may be selected from other secondary aliphatic amines, substituted or branched chain aliphatic amines, for example pinacolyl amine ( 3-amino-2,2-dimethyl-
butane), arylalkylamines, for example benzylamine
(aminotoluene); heterocyclic alkylamines, for example piperonylamine (3,4-methylene-dioxybenzylamine or
dioxyaminotoluene).
The dipotassium salt of 2-nitrodithioacetic acid required as a starting material may be prepared by the method of E Freund, Chem. Ber. 52 , 542 (1919) which produces an ethanol-wet cake. Weights given herein are on a 100% basis, the ethanol being treated as solvent. Analogues of the dipotassium salt of 2-nitrodithioacetic acid, such as those based on butene and propene, can be made by analogous methods.
We prefer to carry out the amination reaction (Reaction I) in a polar solvent, for example, water, methanol, ethanol, isopropanol or dimethyl sulphoxide. On costs and ease of handling, water is the preferred solvent. The reaction concentration (water or other solvent to
dipotassium salt of nitrodithioacetic acid) can be 20:1 to 1:1, but. is preferably 10:1 to 5:1 by weight.
Any ethanol present in the dipotassium salt of
nitrodithioacetic acid as prepared is included as solvent in the above ranges of concentrations and reference to an aqueous solvent includes such minor contents of polar organic solvents. All concentrations quoted herein are in parts by weight unless otherwise stated.
For the amination stage good yields can be obtained using an amine : dipotassium salt of nitrodithioacetic acid molar ratio of 0.8:1 to >2:1 but for the best economics a ratio of 1.1:1 is preferred.
The reaction temperature for the amination reaction can be in the range 0°C to 100°C but it is preferably between 20°C and 60°C. The amination product may be used as a solution as formed or may be recovered.
The alkylation or arylalky lation reaction to convert the thioamide salt to the thio-alkyl derivative (Reaction II) can be carried out in the range 0°C to 60°C, but it is preferably carried out in the range 10°C to 40°C so as to
give an acceptable reaction time and avoid side reactions.
Suitable alkylating or arylalkylating agents are alkyl halides or sulphates and the benzyl halides. Particularly convenient agents are dimethyl sulphate, diethyl sulphate, methyl chloride, methyl bromide, methyl iodide and benzyl chloride. Conveniently the alkylation or ary lalkylation is effected in the presence of a phase transfer agent such as benzy Itrimethylammonium chloride.
During the a lky lation or ary l a lky l ation stage , molar ratios of alkylating/arylalkylating agent : dipotassium salt of nitrodithioacetic acid of 1:1 to >4:1 can be used, but optimum yields are obtained using a molar ratio of 2:1 to 2.5: 1.
The product nitroethenamine may be recovered by
conventional workup procedures such as filtration or, preferably, by extraction of the product directly from the reaction mixture using a suitable organic solvent which is, preferably, a water immiscible chlorinated solvent such as mεthylene chloride, ethylene dichloride or
chlcrcbenzene.This may be followed by drying, concentrating and recrystal lising from a suitable solvent such as propan- 2-ol.
The nitroethenamine produced as above described may be further reacted with an amine to produce a compound having the grouping -NC(=CHNO)NHX where X represents an alkyl arylalkyl or heterocyclicalky 1 group. For example, where the dipotassium salt is dipotassium nitrodithioacetate, where the amine used in Reaction I is piperonylamine and where the alkylated or arylalkylated product of Reaction II is then reacted with 2- [5-(N,N-dimethylaminomethyl)
-2-furanmethylthio]ethylamine the product is the
pharmaceutically active compound niperotidine. Other active materials may be produced using different variants on
Reaction I and II, for example where the same dipotassium salt is used and wherein the amine used in Reaction I is
pinacolylamine and where the product of reaction II is reacted with a range of aryl or heteroaryl amines such as 4- aminopyridine in particular, a range of compounds having hypotensive properties may be produced.
It is understood that it is also within the scope of the present invention to conduct the analogous process to that set out above for the production of compounds
containing the said grouping -NC(=CHNO)NHX wherein the amination of Reaction I and the further amination are
reversed in position. This concept of an analogous process extends over the full range of amines described above as appropriate to Reaction I and to the further amination.
In order that the present invention may more readily be understood, certain preparations in accordance therewith will now be described in detail.
EXAMPLE 1
N Benzyl-1-methylthio-2-nitroethenamine
Dipotassium nitrodithioacetate (64.7 g) dissolved in 280 ml of water was heated to 40°C and benzylamine (48.7g) was then added over 1 hour. After heating to 60°C and
maintaining this temperature for 4 hours the reaction mixture was cooled to ambient temperatures and stirred overnight. Benzyltrimethyl ammonium chloride (4g), was then charged followed by dimethyl sulphate (106g) over one hour. After stirring for a further 6 hours, the precipitated solid was filtered off and recrystallised from 2-propanol to give 31g (46%) of the title compound (m.p. 112°C).
EXAMPLE 2
N , N Dimethyl-1-methylthio-2-nitroethenamine
To a solution of dipotassium nitrodithioacetate (118g) dissolved in water (630 ml), dimethylamine (1.1 equivalents) was added as a 40% w/w solution in water. After stirring for 6 hours at 20-25°C, benzyltrimethyl ammonium chloride (7g) was charged followed by dimethyl sulphate (175g) over
one hour. After stirring overnight, the reaction mixture was extracted three times with 100 ml aliquots of
dichloromethane. After drying over MgSO4, the combined organic phases were concentrated to a red oil which was chromatographed on a silica gel column, using ethyl acetate as eluant to give, after recrystal lisation from isopropanol, 36g (40%) of the title compound, m.p. 60°C.
EXAMPLE 3
N-(1-methy1-2,2-dimethylpropy1)-1-methylthio-2- nitroetheneamine
To an aqueous solution of dipotassium nitrodithioacetate (300g 15% by weight) was added pinacoly lamine (32g) over 1 hour. After heating to 60°C and maintaining this temperature for 4 hours, the reaction mixture was cooled to ambient temperatures and stirred overnight. Benzyltrimethyl ammonium chloride (3g), was then charged, followed by dimethyl
sulphate (66g) over one hour. After stirring overnight, the reaction mixture was extracted three times with 50ml aliquots of dichloromethane. After drying over MgSO4, the combined organic phases were concentrated and the residue
recrystallised from 2-propanol to give 13g (33%) of the title compound (m.p. 69°C) which is believed tc be ncvel.
EXAMPLE 4
N-(3,4-methylenedioxymethyl) 1-Methylthio-2- nitroethenamine.
A 15% w/w solution of dipotassium nitrodithioacetate (303 g), piperonylamine (45.3 g) and dichloroethane was heated to reflux for one hour. The organic phase was separated off and to the aqueous phase at 20°C,
benzyltrimethyl ammonium chloride (1 g) was added followed by dimethyl sulphate (75 g) which was added over 1 hour. The reaction mixture was stirred overnight and the precipitated title compound recrystallised from acetone to give 24 g (42%) (m.p. 126°C).
Claims
1. A method for the production of a mono-potassium salt useful as an intermediate in the production of N- substituted alkyl- or arylalkyl-nitroethenamines characterised by reacting an amine selected from branched chain primary alkylamines, secondary
alkylamines, arylalkylamines and heterocyclic
alkylamines, wherein the alkyl moieties of said
arylalkylamines and heterocyclic alkylamines are not straight chain primary amines containing a heteroatom in the chain, with the dipotassium salt of a 2- nitrodithio-aliphatic acid.
2. A method as claimed in claim 1 wherein the aliphatic acid is 2-nitrodithioacetic acid.
3. A method as claimed in claim 1 or 2 wherein the amine is selected from dimethylamine, pinacoly lamine, benzylamine and piperonylamine.
4. A method as claimed in any preceding claim carried out in an aqueous or organic polar solvent medium at a reaction concentration of solvent medium to dipotassium salt of 20:1 to 1:1 by weight, a molar ratio of amine to dipotassium salt of 0.8:1 to 2:1 a reaction
temperature of 0°C to 100°C for a duration such that the reaction has substantially completed.
5. A method for the production of an N-substituted S- substituted thionitroethenamine comprising preparing a mono-potassium salt by a method according to any one of claims 1 to 4 alkylating or arylalkylating the monopotassium salt and recovering the product.
6. A method as claimed in claim 5 wherein the alkylation or arylation is conducted by reacting the. monopotassium salt with an agent selected from dimethyl sulphate, diethyl sulphate, methyl chloride, methyl bromide, methyl iodide and benzyl chloride.
7. A method as claimed in claim 6 wherein the alkylation is conducted in the presence of a phase transfer agent.
8. A method as claimed in any one of claims 5 to 7
comprising introducing the alkylating or arylalkylating agent into the mono-potassium salt/solvent mixture produced according to any one of claims 1 to 4.
9. A method as claimed in any one of claims 5 to 8 wherein the molar ratio of alkylating or arylalkyl agent to the dipotassium salt is at least 1:1, the reaction
temperature is from 0°C to 60°C and the reaction duration is such that the reaction has substantially completed.
10. A method as claimed in any one of claims 5 to 9 herein the product nitroethenamine is recovered by filtration.
11. A method as claimed in any one of claims 5 to 9 wherein the product nitroethenamine is recovered by solvent extraction.
12. A method as claimed in claim 8 and wherein the monopotassium salt is produced in aqueous medium wherein the product ethenamine is recovered by extraction in a water immiscible chlorinated organic solvent.
13. A method for the production of a compound containing the grouping -NC(=CHNO2)NHX wherein X represents an alkyl, arylalkyl or heterocyclic alkyl group comprising the steps of firstly reacting the dipotassium salt of a 2-nitrodithioaliphatic acid with an amine selected from branched chain primary alkylamines, secondary alkylamines, arylalkylamines and heterocyclicalkyl amines ,wherein the alkyl moities of said
arylalkylamines and heterocyclic amines are not
straight chain primary amines containing a heteroatom in the chain, to form the mono-potassium salt of the nitrodithioaliphatic acid, secondly alkylating or arylalkylating the said mono-potassium salt and thirdly reacting the said alkylated or arylalkylated salt with an amine.
14. The method analogous to that claimed in claim 15
wherein the said first and third steps are reversed in position.
15. A method as claimed in claim 13 wherein the amine used in the third method step or as claimed in claim 14 wherein the amine used in the first method step is 2-
[5-(N,N-dimethylaminomethyl)-2-furan-methylthio] ethylamine.
16. A method as claimed in claim 15 wherein the salt of the 2-nitrodithioaliphatic acid which is used is
dipotassium nitrodithioacetate wherein in the first or third method steps the amine is piperonylamine and wherein the product is the pharmaceutically active compound niperotidine.
17. As a novel intermediate the product of the method
claimed in claim 5 wherein the dipotassium salt is dipotassium-nitrodithioacetate, the amine is
pinacolylamine and the alkylating agent is a methylating agent, the said product being N-(1-methyl- 2,2-dimethylpropyl)-1-methylthio-2-nitroethenamine. The product of a method as claimed in any one of claims 1 to 16.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP90905245A EP0466733B1 (en) | 1989-04-05 | 1990-04-04 | Preparation of substituted ethenes |
| KR1019910700948A KR920701140A (en) | 1989-04-05 | 1990-04-04 | Method for preparing substituted ethene |
| US07/730,963 US5371247A (en) | 1989-04-05 | 1990-04-04 | Preparation of substituted ethenes |
| DE69011677T DE69011677T2 (en) | 1989-04-05 | 1990-04-04 | METHOD FOR PRODUCING SUBSTITUTED ETHENES. |
| FI914672A FI914672A0 (en) | 1989-04-05 | 1991-10-04 | FRAMSTAELLNING AV SUBSTITUERADE ETEN. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB898907700A GB8907700D0 (en) | 1989-04-05 | 1989-04-05 | Preparation of substituted ethenes |
| GB8907700.2 | 1989-04-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1990012002A1 true WO1990012002A1 (en) | 1990-10-18 |
Family
ID=10654520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB1990/000501 WO1990012002A1 (en) | 1989-04-05 | 1990-04-04 | Preparation of substituted ethenes |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US5371247A (en) |
| EP (1) | EP0466733B1 (en) |
| JP (2) | JP2954270B2 (en) |
| KR (2) | KR920701140A (en) |
| AT (2) | AT400030B (en) |
| BE (1) | BE1003124A5 (en) |
| CA (2) | CA2013841C (en) |
| CH (1) | CH681008A5 (en) |
| DE (2) | DE69011677T2 (en) |
| DK (2) | DK84390A (en) |
| ES (2) | ES2019246A6 (en) |
| FI (2) | FI110939B (en) |
| FR (1) | FR2645535B1 (en) |
| GB (2) | GB8907700D0 (en) |
| GR (1) | GR1001302B (en) |
| HU (3) | HU9203905D0 (en) |
| IE (2) | IE61894B1 (en) |
| IL (1) | IL94002A (en) |
| IN (3) | IN170319B (en) |
| IT (1) | IT1242481B (en) |
| NL (1) | NL194699C (en) |
| PT (1) | PT93659B (en) |
| SE (1) | SE509459C2 (en) |
| WO (1) | WO1990012002A1 (en) |
| ZA (1) | ZA902592B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5112995A (en) * | 1989-04-05 | 1992-05-12 | Glaxo Group Limited | Preparation of substituted ethenes |
| EP0750044A2 (en) * | 1991-11-05 | 1996-12-27 | Transkaryotic Therapies, Inc. | DNA constructs and transfection of cells therewith for homologous recombination |
| US5686588A (en) * | 1995-08-16 | 1997-11-11 | Yoo; Seo Hong | Amine acid salt compounds and process for the production thereof |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001264174A1 (en) | 2000-04-21 | 2001-11-07 | Ioannis Pallikaris | Device for the shaping of a substance on the surface of a cornea |
| CN104119257B (en) * | 2013-04-26 | 2016-08-03 | 石家庄康坦福化工科技有限公司 | A kind of preparation method of 1-methylamino-1-methyl mercapto-2-nitroethylene |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2104071A (en) * | 1981-08-18 | 1983-03-02 | Ausonia Farma Srl | Furan derivatives |
| ES8500618A1 (en) * | 1983-06-21 | 1984-11-16 | Union Quimico Farma | Prepn. of methylamino methylthio nitro-ethene |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1554153A (en) * | 1975-05-15 | 1979-10-17 | Smith Kline French Lab | Process for making 2-amino-2-alkylthionitroethylenes |
| PT76557B (en) * | 1982-04-16 | 1986-01-21 | Inke Sa | Process for preparing furan derivatives and addition salts thereof and of pharmaceutical compositions containing the same |
| GB8415254D0 (en) * | 1984-06-15 | 1984-07-18 | Glaxo Group Ltd | Amine derivatives |
| ES2003781A6 (en) * | 1987-02-06 | 1988-11-16 | Unio Quimico Farmaceutica S A | N-methyl 1-methylthio 2-nitro ethenamine prepn. |
| GB8907700D0 (en) * | 1989-04-05 | 1989-05-17 | Fine Organics Ltd | Preparation of substituted ethenes |
-
1989
- 1989-04-05 GB GB898907700A patent/GB8907700D0/en active Pending
- 1989-04-05 HU HU9203905A patent/HU9203905D0/en unknown
-
1990
- 1990-04-04 KR KR1019910700948A patent/KR920701140A/en not_active Application Discontinuation
- 1990-04-04 US US07/730,963 patent/US5371247A/en not_active Expired - Fee Related
- 1990-04-04 ZA ZA902592A patent/ZA902592B/en unknown
- 1990-04-04 BE BE9000381A patent/BE1003124A5/en not_active IP Right Cessation
- 1990-04-04 IN IN247/MAS/90A patent/IN170319B/en unknown
- 1990-04-04 CH CH1132/90A patent/CH681008A5/fr not_active IP Right Cessation
- 1990-04-04 ES ES9000971A patent/ES2019246A6/en not_active Expired - Fee Related
- 1990-04-04 WO PCT/GB1990/000501 patent/WO1990012002A1/en active IP Right Grant
- 1990-04-04 AT AT0080090A patent/AT400030B/en not_active IP Right Cessation
- 1990-04-04 JP JP2090034A patent/JP2954270B2/en not_active Expired - Lifetime
- 1990-04-04 GB GB9007568A patent/GB2230526B/en not_active Expired - Lifetime
- 1990-04-04 JP JP2505189A patent/JP3003946B2/en not_active Expired - Fee Related
- 1990-04-04 IL IL9400290A patent/IL94002A/en not_active IP Right Cessation
- 1990-04-04 DE DE69011677T patent/DE69011677T2/en not_active Expired - Fee Related
- 1990-04-04 CA CA002013841A patent/CA2013841C/en not_active Expired - Lifetime
- 1990-04-04 US US07/503,987 patent/US5112995A/en not_active Expired - Lifetime
- 1990-04-04 DK DK084390A patent/DK84390A/en not_active Application Discontinuation
- 1990-04-04 HU HU902080A patent/HU207991B/en unknown
- 1990-04-04 KR KR1019900004645A patent/KR0147820B1/en not_active IP Right Cessation
- 1990-04-04 GR GR900100250A patent/GR1001302B/en not_active IP Right Cessation
- 1990-04-04 SE SE9001236A patent/SE509459C2/en not_active IP Right Cessation
- 1990-04-04 FR FR909004313A patent/FR2645535B1/en not_active Expired - Lifetime
- 1990-04-04 HU HU902945A patent/HUT58285A/en unknown
- 1990-04-04 DE DE4010888A patent/DE4010888C2/en not_active Expired - Lifetime
- 1990-04-04 DK DK90905245.8T patent/DK0466733T3/en active
- 1990-04-04 ES ES90905245T patent/ES2057549T3/en not_active Expired - Lifetime
- 1990-04-04 AT AT90905245T patent/ATE110055T1/en not_active IP Right Cessation
- 1990-04-04 IT IT04782990A patent/IT1242481B/en active IP Right Grant
- 1990-04-04 IE IE122290A patent/IE61894B1/en not_active IP Right Cessation
- 1990-04-04 PT PT93659A patent/PT93659B/en not_active IP Right Cessation
- 1990-04-04 CA CA002046293A patent/CA2046293C/en not_active Expired - Fee Related
- 1990-04-04 EP EP90905245A patent/EP0466733B1/en not_active Expired - Lifetime
- 1990-04-04 IE IE122190A patent/IE65395B1/en not_active IP Right Cessation
- 1990-04-04 NL NL9000790A patent/NL194699C/en not_active IP Right Cessation
- 1990-04-04 FI FI901696A patent/FI110939B/en active IP Right Grant
-
1991
- 1991-10-04 FI FI914672A patent/FI914672A0/en not_active Application Discontinuation
- 1991-11-25 IN IN872MA1991 patent/IN173648B/en unknown
- 1991-11-25 IN IN871MA1991 patent/IN173647B/en unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2104071A (en) * | 1981-08-18 | 1983-03-02 | Ausonia Farma Srl | Furan derivatives |
| ES8500618A1 (en) * | 1983-06-21 | 1984-11-16 | Union Quimico Farma | Prepn. of methylamino methylthio nitro-ethene |
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|---|
| CHEMICAL ABSTRACTS, Volume 103, No. 15, 14 October 1985, (Columbus, Ohio, US), see page 683, Abstract 122995u, & ES, A1, 8500618 (Union Quimico Farmaceutica S.A.E.) 16 January 1985 see the Abstract (cited in the application) * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5112995A (en) * | 1989-04-05 | 1992-05-12 | Glaxo Group Limited | Preparation of substituted ethenes |
| EP0750044A2 (en) * | 1991-11-05 | 1996-12-27 | Transkaryotic Therapies, Inc. | DNA constructs and transfection of cells therewith for homologous recombination |
| EP0750044A3 (en) * | 1991-11-05 | 1997-01-15 | Transkaryotic Therapies, Inc. | DNA constructs and transfection of cells therewith for homologous recombination |
| US5686588A (en) * | 1995-08-16 | 1997-11-11 | Yoo; Seo Hong | Amine acid salt compounds and process for the production thereof |
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