UA76127C2 - A process for producing a substituted aniline compound and intermediates for realizing thereof - Google Patents
A process for producing a substituted aniline compound and intermediates for realizing thereof Download PDFInfo
- Publication number
- UA76127C2 UA76127C2 UA2003054401A UA2003054401A UA76127C2 UA 76127 C2 UA76127 C2 UA 76127C2 UA 2003054401 A UA2003054401 A UA 2003054401A UA 2003054401 A UA2003054401 A UA 2003054401A UA 76127 C2 UA76127 C2 UA 76127C2
- Authority
- UA
- Ukraine
- Prior art keywords
- group
- general formula
- compound represented
- following general
- hydrogen atom
- Prior art date
Links
- -1 aniline compound Chemical class 0.000 title claims abstract description 171
- 238000000034 method Methods 0.000 title claims abstract description 71
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 239000000543 intermediate Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 56
- 229960001413 acetanilide Drugs 0.000 claims abstract description 42
- FZERHIULMFGESH-UHFFFAOYSA-N methylenecarboxanilide Natural products CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims abstract description 42
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims abstract description 39
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims abstract description 39
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims abstract description 39
- 125000001041 indolyl group Chemical group 0.000 claims abstract description 16
- 230000001590 oxidative effect Effects 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims description 48
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 48
- 125000001188 haloalkyl group Chemical group 0.000 claims description 47
- 125000005843 halogen group Chemical group 0.000 claims description 47
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 47
- 125000003545 alkoxy group Chemical group 0.000 claims description 46
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 45
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 45
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 25
- 125000005431 alkyl carboxamide group Chemical group 0.000 claims description 24
- 125000004104 aryloxy group Chemical group 0.000 claims description 24
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 23
- 239000012279 sodium borohydride Substances 0.000 claims description 21
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 21
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 20
- 238000003381 deacetylation reaction Methods 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 18
- 230000006196 deacetylation Effects 0.000 claims description 18
- 230000003647 oxidation Effects 0.000 claims description 16
- 238000007254 oxidation reaction Methods 0.000 claims description 16
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 14
- 230000003993 interaction Effects 0.000 claims description 11
- 229910052770 Uranium Inorganic materials 0.000 claims description 7
- CVNDJYZTTMPSSQ-UHFFFAOYSA-N [2-(methoxymethyl)phenyl]hydrazine Chemical compound COCC1=CC=CC=C1NN CVNDJYZTTMPSSQ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052785 arsenic Inorganic materials 0.000 claims description 6
- 238000002955 isolation Methods 0.000 claims description 6
- 238000011084 recovery Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 230000000850 deacetylating effect Effects 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 150
- 238000006243 chemical reaction Methods 0.000 description 75
- 239000002904 solvent Substances 0.000 description 53
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 45
- 239000000203 mixture Substances 0.000 description 38
- 238000002360 preparation method Methods 0.000 description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
- 239000011541 reaction mixture Substances 0.000 description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical class CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 18
- 238000006722 reduction reaction Methods 0.000 description 18
- 239000012044 organic layer Substances 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 238000000605 extraction Methods 0.000 description 15
- 239000010410 layer Substances 0.000 description 15
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N hydrochloric acid Substances Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 13
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 238000004440 column chromatography Methods 0.000 description 12
- MRPUESHNMJXBDD-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)propan-2-one Chemical compound COC1=CC(OC)=NC(CC(C)=O)=N1 MRPUESHNMJXBDD-UHFFFAOYSA-N 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 11
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 10
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- HKMCYGKIBUUALH-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-3-oxo-n-phenylpropanamide Chemical compound COC1=CC(OC)=NC(C(=O)CC(=O)NC=2C=CC=CC=2)=N1 HKMCYGKIBUUALH-UHFFFAOYSA-N 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 235000019270 ammonium chloride Nutrition 0.000 description 9
- 239000000741 silica gel Substances 0.000 description 9
- 229910002027 silica gel Inorganic materials 0.000 description 9
- CJBAGZDMKLQHFD-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-1h-indole Chemical compound COC1=CC(OC)=NC(C=2C3=CC=CC=C3NC=2C)=N1 CJBAGZDMKLQHFD-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 7
- 238000004817 gas chromatography Methods 0.000 description 7
- 230000002363 herbicidal effect Effects 0.000 description 7
- 239000012286 potassium permanganate Substances 0.000 description 7
- 230000035484 reaction time Effects 0.000 description 7
- 239000011592 zinc chloride Substances 0.000 description 7
- 235000005074 zinc chloride Nutrition 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 235000011054 acetic acid Nutrition 0.000 description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- YILLIHNRNIMHJY-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-7-(methoxymethyl)-2-methyl-1h-indole Chemical compound CC=1NC=2C(COC)=CC=CC=2C=1C1=NC(OC)=CC(OC)=N1 YILLIHNRNIMHJY-UHFFFAOYSA-N 0.000 description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- CJUJMMAMUMDDJH-UHFFFAOYSA-N (2-aminophenyl)-(4,6-dimethoxypyrimidin-2-yl)methanone Chemical compound COC1=CC(OC)=NC(C(=O)C=2C(=CC=CC=2)N)=N1 CJUJMMAMUMDDJH-UHFFFAOYSA-N 0.000 description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- VEIMVOKKWWOWBM-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-2,7-dimethyl-1h-indole Chemical compound COC1=CC(OC)=NC(C=2C3=CC=CC(C)=C3NC=2C)=N1 VEIMVOKKWWOWBM-UHFFFAOYSA-N 0.000 description 4
- VQXCUEGJQYQNEO-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-7-ethyl-2-methyl-1h-indole Chemical compound CC=1NC=2C(CC)=CC=CC=2C=1C1=NC(OC)=CC(OC)=N1 VQXCUEGJQYQNEO-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 239000010446 mirabilite Substances 0.000 description 4
- 239000012046 mixed solvent Substances 0.000 description 4
- 239000002798 polar solvent Substances 0.000 description 4
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- QZYKNQASNNLMQJ-UHFFFAOYSA-N 1-pyrimidin-2-ylpropan-2-one Chemical compound CC(=O)CC1=NC=CC=N1 QZYKNQASNNLMQJ-UHFFFAOYSA-N 0.000 description 3
- PZKQOBUGIDGJFX-UHFFFAOYSA-N 3-(4,6-dimethoxypyrimidin-2-yl)-5-methoxy-2-methyl-1h-indole Chemical compound C12=CC(OC)=CC=C2NC(C)=C1C1=NC(OC)=CC(OC)=N1 PZKQOBUGIDGJFX-UHFFFAOYSA-N 0.000 description 3
- QRUKOYWDGNQFHW-UHFFFAOYSA-N 3-(4-chloro-4,6-dimethoxy-1h-pyrimidin-2-yl)-3-oxo-n-phenylpropanamide Chemical compound N1C(OC)=CC(Cl)(OC)N=C1C(=O)CC(=O)NC1=CC=CC=C1 QRUKOYWDGNQFHW-UHFFFAOYSA-N 0.000 description 3
- XWDNMBWEWNQSMC-UHFFFAOYSA-N 5-chloro-3-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-1h-indole Chemical compound COC1=CC(OC)=NC(C=2C3=CC(Cl)=CC=C3NC=2C)=N1 XWDNMBWEWNQSMC-UHFFFAOYSA-N 0.000 description 3
- 229910015900 BF3 Inorganic materials 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001408 amides Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- JHPOWXCLWLEKBY-UHFFFAOYSA-N (2-ethylphenyl)hydrazine Chemical compound CCC1=CC=CC=C1NN JHPOWXCLWLEKBY-UHFFFAOYSA-N 0.000 description 2
- ZHERWZMAGGWSIX-UHFFFAOYSA-N 2-(methoxymethyl)aniline Chemical compound COCC1=CC=CC=C1N ZHERWZMAGGWSIX-UHFFFAOYSA-N 0.000 description 2
- OEVVLQBCEVMGGM-UHFFFAOYSA-N 3-(4-chloro-4,6-dimethoxy-1h-pyrimidin-2-yl)-3-hydroxy-n-phenylpropanamide Chemical compound N1C(OC)=CC(Cl)(OC)N=C1C(O)CC(=O)NC1=CC=CC=C1 OEVVLQBCEVMGGM-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 150000008061 acetanilides Chemical class 0.000 description 2
- 150000001243 acetic acids Chemical class 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013058 crude material Substances 0.000 description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002168 ethanoic acid esters Chemical class 0.000 description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 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
- 238000001914 filtration Methods 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 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 description 2
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 2
- 229940067157 phenylhydrazine Drugs 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 238000003797 solvolysis reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- BDSHNNKBWNAZIM-UHFFFAOYSA-N (2,4-dimethylphenyl)hydrazine Chemical compound CC1=CC=C(NN)C(C)=C1 BDSHNNKBWNAZIM-UHFFFAOYSA-N 0.000 description 1
- GHGPIPTUDQZJJS-UHFFFAOYSA-N (2-chlorophenyl)hydrazine Chemical compound NNC1=CC=CC=C1Cl GHGPIPTUDQZJJS-UHFFFAOYSA-N 0.000 description 1
- FGODPVCKFLEVFG-UHFFFAOYSA-N (2-methoxyphenyl)hydrazine Chemical compound COC1=CC=CC=C1NN FGODPVCKFLEVFG-UHFFFAOYSA-N 0.000 description 1
- KJGFNDCSTWGUDT-UHFFFAOYSA-N (2-methylanilino)azanium;chloride Chemical compound Cl.CC1=CC=CC=C1NN KJGFNDCSTWGUDT-UHFFFAOYSA-N 0.000 description 1
- SCZGZDLUGUYLRV-UHFFFAOYSA-N (2-methylphenyl)hydrazine Chemical compound CC1=CC=CC=C1NN SCZGZDLUGUYLRV-UHFFFAOYSA-N 0.000 description 1
- JYPNYAHCNKRLHG-UHFFFAOYSA-N (4-ethylphenyl)hydrazine Chemical compound CCC1=CC=C(NN)C=C1 JYPNYAHCNKRLHG-UHFFFAOYSA-N 0.000 description 1
- PVRSIFAEUCUJPK-UHFFFAOYSA-N (4-methoxyphenyl)hydrazine Chemical compound COC1=CC=C(NN)C=C1 PVRSIFAEUCUJPK-UHFFFAOYSA-N 0.000 description 1
- XAMBIJWZVIZZOG-UHFFFAOYSA-N (4-methylphenyl)hydrazine Chemical compound CC1=CC=C(NN)C=C1 XAMBIJWZVIZZOG-UHFFFAOYSA-N 0.000 description 1
- ZYATZFJUOXJFPY-UHFFFAOYSA-N (4-propan-2-ylphenyl)hydrazine Chemical compound CC(C)C1=CC=C(NN)C=C1 ZYATZFJUOXJFPY-UHFFFAOYSA-N 0.000 description 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 description 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- XZWYEAUEGLJAJC-UHFFFAOYSA-N 1-(4,6-dichloropyrimidin-2-yl)propan-2-one Chemical compound CC(=O)CC1=NC(Cl)=CC(Cl)=N1 XZWYEAUEGLJAJC-UHFFFAOYSA-N 0.000 description 1
- CJHSVBOGIGFNLR-UHFFFAOYSA-N 1-(4,6-diethoxypyrimidin-2-yl)propan-2-one Chemical compound CCOC1=CC(OCC)=NC(CC(C)=O)=N1 CJHSVBOGIGFNLR-UHFFFAOYSA-N 0.000 description 1
- PPNKLVXLKPRYIR-UHFFFAOYSA-N 1-(4,6-dimethoxy-5-nitropyrimidin-2-yl)propan-2-one Chemical compound COC1=NC(CC(C)=O)=NC(OC)=C1[N+]([O-])=O PPNKLVXLKPRYIR-UHFFFAOYSA-N 0.000 description 1
- RLFDJIVMZZXXPH-UHFFFAOYSA-N 1-(5-ethyl-4,6-dimethoxypyrimidin-2-yl)propan-2-one Chemical compound CCC1=C(OC)N=C(CC(C)=O)N=C1OC RLFDJIVMZZXXPH-UHFFFAOYSA-N 0.000 description 1
- IPTRRTCPDSCNOI-UHFFFAOYSA-N 2-(benzenesulfonyl)-4,6-dimethoxypyrimidine Chemical compound COC1=CC(OC)=NC(S(=O)(=O)C=2C=CC=CC=2)=N1 IPTRRTCPDSCNOI-UHFFFAOYSA-N 0.000 description 1
- IFTCDVWETRBXGT-UHFFFAOYSA-N 2-(benzenesulfonyl)-4,6-dimethylpyrimidine Chemical compound CC1=CC(C)=NC(S(=O)(=O)C=2C=CC=CC=2)=N1 IFTCDVWETRBXGT-UHFFFAOYSA-N 0.000 description 1
- VVCMGAUPZIKYTH-VGHSCWAPSA-N 2-acetyloxybenzoic acid;[(2s,3r)-4-(dimethylamino)-3-methyl-1,2-diphenylbutan-2-yl] propanoate;1,3,7-trimethylpurine-2,6-dione Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O.CN1C(=O)N(C)C(=O)C2=C1N=CN2C.C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 VVCMGAUPZIKYTH-VGHSCWAPSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- ITDVJJVNAASTRS-UHFFFAOYSA-N 4,6-dimethoxy-2-methylsulfonylpyrimidine Chemical compound COC1=CC(OC)=NC(S(C)(=O)=O)=N1 ITDVJJVNAASTRS-UHFFFAOYSA-N 0.000 description 1
- FPSPPRZKBUVEJQ-UHFFFAOYSA-N 4,6-dimethoxypyrimidine Chemical compound COC1=CC(OC)=NC=N1 FPSPPRZKBUVEJQ-UHFFFAOYSA-N 0.000 description 1
- XXNOGQJZAOXWAQ-UHFFFAOYSA-N 4-chlorophenylhydrazine Chemical compound NNC1=CC=C(Cl)C=C1 XXNOGQJZAOXWAQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- JJORFKLVGMELDN-UHFFFAOYSA-N [2-amino-3-(methoxymethyl)phenyl]-(4,6-dimethoxypyrimidin-2-yl)methanol Chemical compound COCC1=CC=CC(C(O)C=2N=C(OC)C=C(OC)N=2)=C1N JJORFKLVGMELDN-UHFFFAOYSA-N 0.000 description 1
- FHZRXTRVRCXCCK-UHFFFAOYSA-N [2-amino-3-(methoxymethyl)phenyl]-(4,6-dimethoxypyrimidin-2-yl)methanone Chemical compound COCC1=CC=CC(C(=O)C=2N=C(OC)C=C(OC)N=2)=C1N FHZRXTRVRCXCCK-UHFFFAOYSA-N 0.000 description 1
- WPYMGNFTVGSSAE-UHFFFAOYSA-N [4-(methoxymethyl)phenyl]hydrazine Chemical compound COCC1=CC=C(NN)C=C1 WPYMGNFTVGSSAE-UHFFFAOYSA-N 0.000 description 1
- DBNLGTYGKCMLLR-UHFFFAOYSA-N [4-(trifluoromethyl)phenyl]hydrazine Chemical compound NNC1=CC=C(C(F)(F)F)C=C1 DBNLGTYGKCMLLR-UHFFFAOYSA-N 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000005841 biaryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- IUXRSXYEOYUWMC-UHFFFAOYSA-N ethyl 4,6-dimethoxy-2-(2-oxopropyl)pyrimidine-5-carboxylate Chemical compound CCOC(=O)C1=C(OC)N=C(CC(C)=O)N=C1OC IUXRSXYEOYUWMC-UHFFFAOYSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- PUVXAQCVNJUHKG-UHFFFAOYSA-N methyl 4-hydrazinylbenzoate Chemical compound COC(=O)C1=CC=C(NN)C=C1 PUVXAQCVNJUHKG-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000011909 oxidative ring-opening Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical group CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/10—Hydrazines
- C07C243/22—Hydrazines having nitrogen atoms of hydrazine groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/30—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000316345 | 2000-10-17 | ||
| JP2001034216 | 2001-02-09 | ||
| PCT/JP2001/009040 WO2002032882A1 (fr) | 2000-10-17 | 2001-10-15 | Procede de production de compose aniline substituee |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA76127C2 true UA76127C2 (en) | 2006-07-17 |
Family
ID=26602218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2003054401A UA76127C2 (en) | 2000-10-17 | 2001-10-15 | A process for producing a substituted aniline compound and intermediates for realizing thereof |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US7271263B2 (de) |
| EP (2) | EP2025665B1 (de) |
| JP (1) | JP4189217B2 (de) |
| KR (1) | KR100720220B1 (de) |
| CN (5) | CN1935793B (de) |
| AT (2) | ATE540934T1 (de) |
| AU (2) | AU9593401A (de) |
| BR (1) | BR0114647B1 (de) |
| CA (1) | CA2425531C (de) |
| CZ (1) | CZ304539B6 (de) |
| DE (1) | DE60143102D1 (de) |
| ES (1) | ES2379459T3 (de) |
| HU (1) | HUP0303102A3 (de) |
| IL (2) | IL155486A (de) |
| MX (2) | MX2008009729A (de) |
| NO (2) | NO324704B1 (de) |
| PL (1) | PL209226B1 (de) |
| RU (1) | RU2292338C2 (de) |
| TW (1) | TWI302910B (de) |
| UA (1) | UA76127C2 (de) |
| WO (1) | WO2002032882A1 (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025665B1 (de) * | 2000-10-17 | 2010-09-15 | Ihara Chemical Industry Co., Ltd. | Verfahren zur Herstellung einer substituierten Anilinverbindung |
| JP4615881B2 (ja) * | 2004-03-15 | 2011-01-19 | イハラケミカル工業株式会社 | アニリン化合物の製造方法 |
| JP4545487B2 (ja) * | 2004-05-28 | 2010-09-15 | イハラケミカル工業株式会社 | アニリド化合物の製造方法 |
| JP2006124347A (ja) * | 2004-10-29 | 2006-05-18 | Bayer Cropscience Ag | フェニル２−ピリミジニルケトン類の新規製造方法及びその新規中間体 |
| US7799795B2 (en) * | 2005-06-27 | 2010-09-21 | Amgen Inc. | Aryl nitrile compounds and compositions and their uses in treating inflammatory and related disorders |
| AT502538B1 (de) * | 2005-09-30 | 2007-08-15 | Dsm Fine Chem Austria Gmbh | Verfahren zur herstellung von n-substituierten aminoacetophenonen und folgeprodukten |
| US8034081B2 (en) | 2007-02-06 | 2011-10-11 | CollabComl, LLC | Interspinous dynamic stabilization implant and method of implanting |
| CN110759893B (zh) * | 2018-07-26 | 2022-10-28 | 南开大学 | Hyrtinadine生物碱衍生物及其制备和在抗植物病毒和病菌中的应用 |
| CN111004185A (zh) * | 2019-12-19 | 2020-04-14 | 安徽省化工研究院 | 苯胺类化合物及其制备方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2406799A1 (de) * | 1974-02-11 | 1975-08-21 | Schering Ag | Neue indolderivate und verfahren zu ihrer herstellung |
| US4225711A (en) * | 1978-10-02 | 1980-09-30 | Schering Corporation | Substituted 2-[(methylsulfinyl)acetyl]-3-heterocyclicindoles and their use as immunosuppressants |
| EP0096657B1 (de) * | 1982-06-08 | 1989-04-05 | Ciba-Geigy Ag | 2-Phenyl-, 2-Naphthyl- und 2-Heterocyclylpyrimidine als Gegenmittel zum Schützen von Kulturpflanzen vor durch Herbizide verursachte phytotoxische Schäden |
| JPH0748359A (ja) | 1992-10-16 | 1995-02-21 | Nippon Soda Co Ltd | 縮合ピリミジン誘導体、除草剤および農園芸用殺菌剤 |
| DE19521355A1 (de) | 1995-06-12 | 1996-12-19 | Hoechst Schering Agrevo Gmbh | Sulfonamide, Verfahren zu deren Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| JPH1160562A (ja) | 1997-06-11 | 1999-03-02 | Kumiai Chem Ind Co Ltd | スルホンアニリド誘導体及び除草剤 |
| JP3632947B2 (ja) * | 1998-07-29 | 2005-03-30 | クミアイ化学工業株式会社 | ジフルオロメタンスルホニルアニリド誘導体、その製造方法及びそれを有効成分とする除草剤 |
| ID28214A (id) * | 1998-07-29 | 2001-05-10 | Ihara Chemical Ind Co | Turunan di- atau trifluorometanasulfonil anilida, proses pembuatannya, dan herbisida yang mengandung turunan tersebut sebagai bahan aktif |
| JP3697075B2 (ja) * | 1998-08-21 | 2005-09-21 | クミアイ化学工業株式会社 | トリフルオロメタンスルホニルアニリド誘導体、その製造方法及びそれを有効成分とする除草剤 |
| EP1101769A3 (de) | 1999-11-18 | 2001-10-24 | Pfizer Products Inc. | Stickstoff-enthaltend Erythromycin-Derivate |
| EP2025665B1 (de) * | 2000-10-17 | 2010-09-15 | Ihara Chemical Industry Co., Ltd. | Verfahren zur Herstellung einer substituierten Anilinverbindung |
| CN1262544C (zh) * | 2001-10-15 | 2006-07-05 | 隆萨股份公司 | 1－(嘧啶－2基)丙－2－酮的制备方法 |
| DE60226471D1 (de) * | 2001-10-17 | 2008-06-19 | Lonza Ag | Verfahren zur herstellung von (pyrimidin-2-yl)methylketonen |
-
2001
- 2001-10-15 EP EP08017752A patent/EP2025665B1/de not_active Expired - Lifetime
- 2001-10-15 DE DE60143102T patent/DE60143102D1/de not_active Expired - Lifetime
- 2001-10-15 EP EP01976689A patent/EP1334968B1/de not_active Expired - Lifetime
- 2001-10-15 ES ES01976689T patent/ES2379459T3/es not_active Expired - Lifetime
- 2001-10-15 AU AU9593401A patent/AU9593401A/xx active Pending
- 2001-10-15 CZ CZ2003-1021A patent/CZ304539B6/cs not_active IP Right Cessation
- 2001-10-15 MX MX2008009729A patent/MX2008009729A/es active IP Right Grant
- 2001-10-15 AU AU2001295934A patent/AU2001295934B2/en not_active Ceased
- 2001-10-15 MX MXPA03003275A patent/MXPA03003275A/es active IP Right Grant
- 2001-10-15 AT AT01976689T patent/ATE540934T1/de active
- 2001-10-15 CN CN2006100999069A patent/CN1935793B/zh not_active Expired - Fee Related
- 2001-10-15 BR BRPI0114647-5A patent/BR0114647B1/pt not_active IP Right Cessation
- 2001-10-15 CN CNB2006100999073A patent/CN100439326C/zh not_active Expired - Fee Related
- 2001-10-15 AT AT08017752T patent/ATE481380T1/de active
- 2001-10-15 CN CNB2006100999054A patent/CN100503579C/zh not_active Expired - Fee Related
- 2001-10-15 UA UA2003054401A patent/UA76127C2/uk unknown
- 2001-10-15 KR KR1020037005218A patent/KR100720220B1/ko not_active IP Right Cessation
- 2001-10-15 IL IL155486A patent/IL155486A/en not_active IP Right Cessation
- 2001-10-15 HU HU0303102A patent/HUP0303102A3/hu unknown
- 2001-10-15 US US10/398,025 patent/US7271263B2/en not_active Expired - Fee Related
- 2001-10-15 RU RU2003114411/04A patent/RU2292338C2/ru not_active IP Right Cessation
- 2001-10-15 PL PL362050A patent/PL209226B1/pl unknown
- 2001-10-15 CN CNB2005100517019A patent/CN1288146C/zh not_active Expired - Fee Related
- 2001-10-15 WO PCT/JP2001/009040 patent/WO2002032882A1/ja active Application Filing
- 2001-10-15 CA CA2425531A patent/CA2425531C/en not_active Expired - Fee Related
- 2001-10-15 CN CNB018188575A patent/CN1223587C/zh not_active Expired - Fee Related
- 2001-10-15 JP JP2002536265A patent/JP4189217B2/ja not_active Expired - Fee Related
- 2001-10-16 TW TW090125569A patent/TWI302910B/zh not_active IP Right Cessation
-
2003
- 2003-04-11 NO NO20031683A patent/NO324704B1/no not_active IP Right Cessation
-
2006
- 2006-05-31 US US11/442,970 patent/US7521555B2/en not_active Expired - Fee Related
-
2007
- 2007-04-30 US US11/790,940 patent/US7820861B2/en not_active Expired - Fee Related
- 2007-04-30 US US11/790,939 patent/US7531654B2/en not_active Expired - Fee Related
- 2007-04-30 US US11/790,941 patent/US7504503B2/en not_active Expired - Fee Related
- 2007-08-15 NO NO20074193A patent/NO20074193L/no not_active Application Discontinuation
-
2008
- 2008-07-15 IL IL192827A patent/IL192827A/en not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2961237T3 (es) | Métodos para la preparación de compuestos heterocíclicos de 1,3-benzodioxol | |
| US7521555B2 (en) | Process for producing substituted aniline compound | |
| ES2923278T3 (es) | Intermedios útiles para la síntesis de derivados de aminopirimidinas, proceso de preparación del mismo y proceso de preparación de aminopirimidina derivados utilizando los mismos | |
| EP2980079B1 (de) | Verfahren zur herstellung einer pyridazinonverbindung | |
| ES2933074B2 (es) | Procedimiento de sintesis de 2,4-dimetilpirimidin-5-ol, nuevos intermedios de dicho procedimiento y uso del producto en la sintesis de lemborexant | |
| AU2006203037B2 (en) | Process for production of substituted aniline compound | |
| MX2010011025A (es) | Sintesis de dihidrotieno [3,2-d] pirimidina-dioles y pirimidina-dioles similares. | |
| JP2010515706A (ja) | アリール置換縮合ピリミジンの製造方法 | |
| JP2005035932A (ja) | ４−置換ピラゾロ［１，５−ａ］ピリミジンジオン誘導体の製造方法 | |
| SK72196A3 (en) | Method for producing 1-{£2-(cyclopropylcarbonyl)- phenyl| sulfamoyl}-3-(4,6-dialkoxy-2-pyrimidinyl) of urea and intermediate products of this method |