SU492074A3 - Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей, или их функциональных аминопроизводных - Google Patents

Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей, или их функциональных аминопроизводных

Info

Publication number: SU492074A3
Authority: SU; USSR - Soviet Union
Prior art keywords: salts; derivatives; acid; aminophenyl; obtaining
Prior art date: 1969-03-18

Application number

SU1947365A

Other languages

English (en)

Russian (ru)

Inventor

Вильем Джеймс Карни Ричэд

Дэ Стивенс Джорж

Original Assignee

Циба-Гейги Аг (Фирма)

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1969-03-18

Filing date

1970-03-17

Publication date

1975-11-15

1969-09-12 Priority claimed from CH1383069A external-priority patent/CH574921A5/de

1970-03-17 Application filed by Циба-Гейги Аг (Фирма) filed Critical Циба-Гейги Аг (Фирма)

1975-11-15 Application granted granted Critical

1975-11-15 Publication of SU492074A3 publication Critical patent/SU492074A3/ru

Links

-1 aminophenyl Chemical group 0.000 title description 20
150000003839 salts Chemical class 0.000 title description 19
238000000034 method Methods 0.000 title description 7
150000001412 amines Chemical class 0.000 title description 5
150000001735 carboxylic acids Chemical class 0.000 title 1
239000002253 acid Substances 0.000 description 16
150000001875 compounds Chemical class 0.000 description 11
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
150000007513 acids Chemical class 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
235000019441 ethanol Nutrition 0.000 description 6
239000000203 mixture Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
229910021529 ammonia Inorganic materials 0.000 description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000008044 alkali metal hydroxides Chemical class 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
235000011167 hydrochloric acid Nutrition 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
150000007522 mineralic acids Chemical class 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
MJUBBJUFXLSRNI-UHFFFAOYSA-N 2-(2,5-dihydropyrrol-1-yl)-2-phenylpropanoic acid Chemical compound C=1C=CC=CC=1C(C)(C(O)=O)N1CC=CC1 MJUBBJUFXLSRNI-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
150000001204 N-oxides Chemical class 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
150000001721 carbon Chemical group 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
150000002825 nitriles Chemical class 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
239000000725 suspension Substances 0.000 description 2
SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
WDRFYIPWHMGQPN-UHFFFAOYSA-N 2-chloroisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(Cl)C(=O)C2=C1 WDRFYIPWHMGQPN-UHFFFAOYSA-N 0.000 description 1
BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 1
WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 1
RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 description 1
125000005274 4-hydroxybenzoic acid group Chemical group 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
241001139947 Mida Species 0.000 description 1
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
239000004157 Nitrosyl chloride Substances 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
TXTQARDVRPFFHL-UHFFFAOYSA-N [Sb].[H][H] Chemical compound [Sb].[H][H] TXTQARDVRPFFHL-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
238000006136 alcoholysis reaction Methods 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
MQWDTXAOPTYTLC-UHFFFAOYSA-N butyl 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylate Chemical group C1CC(C(=O)OCCCC)(C=2C=CC=CC=2)CCN1CCC(C#N)(C=1C=CC=CC=1)C1=CC=CC=C1 MQWDTXAOPTYTLC-UHFFFAOYSA-N 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 1
AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
238000001640 fractional crystallisation Methods 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
UWYVPFMHMJIBHE-OWOJBTEDSA-N hydroxymaleic acid group Chemical group O/C(/C(=O)O)=C/C(=O)O UWYVPFMHMJIBHE-OWOJBTEDSA-N 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
150000004966 inorganic peroxy acids Chemical class 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
MBHINSULENHCMF-UHFFFAOYSA-N n,n-dimethylpropanamide Chemical compound CCC(=O)N(C)C MBHINSULENHCMF-UHFFFAOYSA-N 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
229960002715 nicotine Drugs 0.000 description 1
SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 description 1
235000019392 nitrosyl chloride Nutrition 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000004967 organic peroxy acids Chemical class 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
NHKJPPKXDNZFBJ-UHFFFAOYSA-N phenyllithium Chemical compound [Li]C1=CC=CC=C1 NHKJPPKXDNZFBJ-UHFFFAOYSA-N 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
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 description 1
SYRHIZPPCHMRIT-UHFFFAOYSA-N tin(4+) Chemical compound [Sn+4] SYRHIZPPCHMRIT-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Pyrrole Compounds (AREA)
Hydrogenated Pyridines (AREA)

SU1947365A 1969-03-18 1970-03-17 Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей, или их функциональных аминопроизводных SU492074A3 (ru)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US80834369A	1969-03-18	1969-03-18
CH1383069A CH574921A5 (en)	1969-09-12	1969-09-12	Anti-inflammatory alpha-aminophenyl carboxylic acids

Publications (1)

Publication Number	Publication Date
SU492074A3 true SU492074A3 (ru)	1975-11-15

Family

ID=25713101

Family Applications (11)

Application Number	Title	Priority Date	Filing Date
SU1947365A SU492074A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей, или их функциональных аминопроизводных
SU1707197A SU458977A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)-алифатических производных карбоновых кислот, или их солей, или их -окисей
SU1701189A SU451236A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей,или их -окисей
SU1688521A SU500749A3 (ru)	1969-03-18	1970-03-17	Способ получени производных (аминофенил)-алифатических карбоновых кислот или их солей или -окисей
SU1701188A SU470110A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей или их -окисей
SU1707907A SU480216A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей,или их -окисей
SU1703512A SU507226A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей,или их -окисей
SU1700721A SU507227A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил-)-алифатических производных карбоновых кислот или их солей, или их -окисей
SU1413657A SU511850A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических карбоновых кислот
SU1703107A SU471713A3 (ru)	1969-03-18	1970-03-17	Способ получени -/аминофенил/алифатических производных карбоновых кислот или их солей,или их -окисей
SU1707517A SU516346A3 (ru)	1969-03-18	1971-10-21	Способ получени -(аминофенил)-алифатических производных карбоновых кислот, или их солей, или их -окисей

Family Applications After (10)

Application Number	Title	Priority Date	Filing Date
SU1707197A SU458977A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)-алифатических производных карбоновых кислот, или их солей, или их -окисей
SU1701189A SU451236A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей,или их -окисей
SU1688521A SU500749A3 (ru)	1969-03-18	1970-03-17	Способ получени производных (аминофенил)-алифатических карбоновых кислот или их солей или -окисей
SU1701188A SU470110A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей или их -окисей
SU1707907A SU480216A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей,или их -окисей
SU1703512A SU507226A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей,или их -окисей
SU1700721A SU507227A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил-)-алифатических производных карбоновых кислот или их солей, или их -окисей
SU1413657A SU511850A3 (ru)	1969-03-18	1970-03-17	Способ получени -(аминофенил)алифатических карбоновых кислот
SU1703107A SU471713A3 (ru)	1969-03-18	1970-03-17	Способ получени -/аминофенил/алифатических производных карбоновых кислот или их солей,или их -окисей
SU1707517A SU516346A3 (ru)	1969-03-18	1971-10-21	Способ получени -(аминофенил)-алифатических производных карбоновых кислот, или их солей, или их -окисей

Country Status (3)

Country	Link
JP (2)	JPS5434727B1 (2)
BE (1)	BE747468R (2)
SU (11)	SU492074A3 (2)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3500710A1 (de) *	1984-01-18	1985-07-25	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von phenylessigsaeureestern

1970
- 1970-03-17 SU SU1947365A patent/SU492074A3/ru active
- 1970-03-17 SU SU1707197A patent/SU458977A3/ru active
- 1970-03-17 SU SU1701189A patent/SU451236A3/ru active
- 1970-03-17 SU SU1688521A patent/SU500749A3/ru active
- 1970-03-17 SU SU1701188A patent/SU470110A3/ru active
- 1970-03-17 SU SU1707907A patent/SU480216A3/ru active
- 1970-03-17 BE BE747468A patent/BE747468R/xx active
- 1970-03-17 SU SU1703512A patent/SU507226A3/ru active
- 1970-03-17 SU SU1700721A patent/SU507227A3/ru active
- 1970-03-17 SU SU1413657A patent/SU511850A3/ru active
- 1970-03-17 SU SU1703107A patent/SU471713A3/ru active
1971
- 1971-10-21 SU SU1707517A patent/SU516346A3/ru active
1978
- 1978-03-31 JP JP3696578A patent/JPS5434727B1/ja active Pending
- 1978-03-31 JP JP3696478A patent/JPS5425025B1/ja active Pending

Also Published As

Publication number	Publication date
SU471713A3 (ru)	1975-05-25
JPS5434727B1 (2)	1979-10-29
SU516346A3 (ru)	1976-05-30
SU451236A3 (ru)	1974-11-25
SU458977A3 (ru)	1975-01-30
BE747468R (fr)	1970-09-17
SU500749A3 (ru)	1976-01-25
SU480216A3 (ru)	1975-08-05
JPS5425025B1 (2)	1979-08-24
SU507227A3 (ru)	1976-03-15
SU507226A3 (ru)	1976-03-15
SU470110A3 (ru)	1975-05-05
SU511850A3 (ru)	1976-04-25

Publication	Publication Date	Title
Ainsworth	1955	The condensation of aryl carboxylic acid hydrazides with orthoesters
Grimmel et al.	1946	Phosphazo compounds and their use in preparing amides
US3238224A (en)	1966-03-01	Production of 6, 8-dithiooctanoyl amides
CA1066711A (en)	1979-11-20	Thiophene derivatives
US3201472A (en)	1965-08-17	Tertiary-amino-alkylated primary amines
SU559642A3 (ru)	1977-05-25	Способ получени алканоламинов или их солей в виде рацематов или оптически - активных антиподов
SU468399A3 (ru)	1975-04-25	Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей или их окисей
SU492074A3 (ru)	1975-11-15	Способ получени -(аминофенил)-алифатических производных карбоновых кислот или их солей, или их функциональных аминопроизводных
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US3151160A (en)	1964-09-29	Process for the preparation of tertiaryamino-alkylated primary amines
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US3624096A (en)	1971-11-30	A process for producing certain amide derivatives of pyridine and reducing said amides to corresponding amines
US3725422A (en)	1973-04-03	New organic sulfur compounds and methods for their production
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IE64009B1 (en)	1995-06-28	A method for the sequential oxidation of substituted-8-hydroxy-quinolines to produce substituted-pyridine-2,3-dicarboxylic acids
US4292431A (en)	1981-09-29	Process for the production of hydroxymethylimidazoles
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US5952494A (en)	1999-09-14	Method for the preparation of pyrido benzoxazine derivatives
SU468400A3 (ru)	1975-04-25	Способ получени (аминофенил)-алифатических производных карбоновых кислот или их солей,или их -окисей
SU473357A3 (ru)	1975-06-05	Способ получени -(аминофенил)алифатических карбоновых кислот или их производных,или их солей
US3417089A (en)	1968-12-17	Enol betaines and process for preparing the same
US3712906A (en)	1973-01-23	Derivatives of 4-(aminoethane-sulfonylamino)-antipyrine
SU458978A3 (ru)	1975-01-30	Способ получени -(аминофенил)алифатических карбоновых кислот