CH626335A5 - - Google Patents

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Info

Publication number: CH626335A5
Authority: CH; Switzerland
Prior art keywords: autoclave; carbon monoxide; selenium; product; reaction
Prior art date: 1975-04-23

Application number

CH500676A

Other languages

English (en)

Italian (it)

Inventor

Paolo Koch

Bartolomeo Anfossi

Original Assignee

Anic Spa

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.)

1975-04-23

Filing date

1976-04-21

Publication date

1981-11-13

1976-04-21 Application filed by Anic Spa filed Critical Anic Spa

1981-11-13 Publication of CH626335A5 publication Critical patent/CH626335A5/it

Links

UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 48
229910002091 carbon monoxide Inorganic materials 0.000 claims description 48
239000011669 selenium Substances 0.000 claims description 43
238000006243 chemical reaction Methods 0.000 claims description 39
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 37
229910052711 selenium Inorganic materials 0.000 claims description 37
238000000034 method Methods 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 7
150000003560 thiocarbamic acids Chemical class 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
238000002360 preparation method Methods 0.000 claims description 4
230000003197 catalytic effect Effects 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
150000008427 organic disulfides Chemical class 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000002877 alkyl aryl group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
150000003512 tertiary amines Chemical class 0.000 claims description 2
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 72
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 58
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 48
239000000047 product Substances 0.000 description 44
239000000155 melt Substances 0.000 description 24
238000003756 stirring Methods 0.000 description 14
ONJROLGQWMBXAP-UHFFFAOYSA-N 2-methyl-1-(2-methylpropyldisulfanyl)propane Chemical compound CC(C)CSSCC(C)C ONJROLGQWMBXAP-UHFFFAOYSA-N 0.000 description 13
238000004458 analytical method Methods 0.000 description 13
239000000203 mixture Substances 0.000 description 12
239000002904 solvent Substances 0.000 description 12
238000010521 absorption reaction Methods 0.000 description 11
239000003208 petroleum Substances 0.000 description 10
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
229910052717 sulfur Inorganic materials 0.000 description 8
WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 7
GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 6
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 5
238000001816 cooling Methods 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
238000000921 elemental analysis Methods 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
238000001914 filtration Methods 0.000 description 4
239000012948 isocyanate Substances 0.000 description 4
150000002513 isocyanates Chemical class 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000007787 solid Substances 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 3
-1 amino compound Chemical class 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical compound SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 description 3
239000007789 gas Substances 0.000 description 3
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 3
GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 description 2
VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 description 2
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 description 1
DMSHKWHLXNDUST-UHFFFAOYSA-N (4-methylphenyl)urea Chemical compound CC1=CC=C(NC(N)=O)C=C1 DMSHKWHLXNDUST-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
CMWSRWTXVQLHNX-UHFFFAOYSA-N 2-methyl-1-(2-methylpropylsulfanyl)propane Chemical compound CC(C)CSCC(C)C CMWSRWTXVQLHNX-UHFFFAOYSA-N 0.000 description 1
PNPCRKVUWYDDST-UHFFFAOYSA-N 3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1 PNPCRKVUWYDDST-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
CUDSBWGCGSUXDB-UHFFFAOYSA-N Dibutyl disulfide Chemical compound CCCCSSCCCC CUDSBWGCGSUXDB-UHFFFAOYSA-N 0.000 description 1
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
229910002090 carbon oxide Inorganic materials 0.000 description 1
230000006315 carbonylation Effects 0.000 description 1
238000005810 carbonylation reaction Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
DAEJUXVTANZZKM-UHFFFAOYSA-N s-(2-hydroxyethyl) n-cyclohexylcarbamothioate Chemical compound OCCSC(=O)NC1CCCCC1 DAEJUXVTANZZKM-UHFFFAOYSA-N 0.000 description 1
LADHHNUVWRWPRH-UHFFFAOYSA-N s-methyl carbamothioate Chemical compound CSC(N)=O LADHHNUVWRWPRH-UHFFFAOYSA-N 0.000 description 1
YYTUUFAEVJPDAA-UHFFFAOYSA-N s-methyl n-butylcarbamothioate Chemical compound CCCCNC(=O)SC YYTUUFAEVJPDAA-UHFFFAOYSA-N 0.000 description 1
JVXFWBQTVKQAOE-UHFFFAOYSA-N s-phenyl carbamothioate Chemical compound NC(=O)SC1=CC=CC=C1 JVXFWBQTVKQAOE-UHFFFAOYSA-N 0.000 description 1
JWWKLULUFDIQGC-UHFFFAOYSA-N s-phenyl n-cyclohexylcarbamothioate Chemical compound C=1C=CC=CC=1SC(=O)NC1CCCCC1 JWWKLULUFDIQGC-UHFFFAOYSA-N 0.000 description 1
GHVNOMLMOUKJOC-UHFFFAOYSA-N s-phenyl n-propan-2-ylcarbamothioate Chemical compound CC(C)NC(=O)SC1=CC=CC=C1 GHVNOMLMOUKJOC-UHFFFAOYSA-N 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/02—Monothiocarbamic acids; Derivatives thereof
- C07C333/04—Monothiocarbamic acids; Derivatives thereof having nitrogen atoms of thiocarbamic groups bound to hydrogen atoms or to acyclic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/02—Monothiocarbamic acids; Derivatives thereof
- C07C333/08—Monothiocarbamic acids; Derivatives thereof having nitrogen atoms of thiocarbamic groups bound to carbon atoms of six-membered aromatic rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

CH500676A 1975-04-23 1976-04-21 CH626335A5 (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT22617/75A IT1037578B (it)	1975-04-23	1975-04-23	Procedimento per la sintesi di esteri di acidi tiocarbammici

Publications (1)

Publication Number	Publication Date
CH626335A5 true CH626335A5 (sv)	1981-11-13

Family

ID=11198480

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH500676A CH626335A5 (sv)	1975-04-23	1976-04-21

Country Status (19)

Country	Link
US (1)	US4020093A (sv)
JP (1)	JPS51128919A (sv)
AU (1)	AU502237B2 (sv)
BE (1)	BE841008A (sv)
CA (1)	CA1074808A (sv)
CH (1)	CH626335A5 (sv)
DD (1)	DD125345A5 (sv)
DE (1)	DE2617917C3 (sv)
DK (1)	DK179976A (sv)
ES (1)	ES447393A1 (sv)
FR (1)	FR2308618A1 (sv)
GB (1)	GB1492335A (sv)
IE (1)	IE43468B1 (sv)
IT (1)	IT1037578B (sv)
LU (1)	LU74810A1 (sv)
NL (1)	NL166257C (sv)
NO (1)	NO141716C (sv)
SE (1)	SE431980B (sv)
ZA (1)	ZA762220B (sv)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2725146A1 (de) *	1977-06-03	1978-12-14	Basf Ag	Diurethane und herbizide
IT1197460B (it) *	1982-02-09	1988-11-30	Anic Spa	Procedimento per la sintesi di esteri di acidi tiocarbammici
JPS5955866A (ja) *	1982-09-24	1984-03-31	Mitsubishi Chem Ind Ltd	チオカルバミン酸誘導体の製造法
CN101921218B (zh) *	2010-09-06	2013-04-24	江苏食品职业技术学院	一种硫代氨基甲酸酯的制备方法
CN117861700B (zh) *	2024-03-13	2024-05-07	东营海瑞宝新材料有限公司	一种二甲硫基甲苯二胺烷基化反应催化剂及其制备方法

1975
- 1975-04-23 IT IT22617/75A patent/IT1037578B/it active
1976
- 1976-04-13 ZA ZA762220A patent/ZA762220B/xx unknown
- 1976-04-20 CA CA250,556A patent/CA1074808A/en not_active Expired
- 1976-04-20 AU AU13113/76A patent/AU502237B2/en not_active Expired
- 1976-04-20 US US05/678,669 patent/US4020093A/en not_active Expired - Lifetime
- 1976-04-21 ES ES447393A patent/ES447393A1/es not_active Expired
- 1976-04-21 CH CH500676A patent/CH626335A5/it not_active IP Right Cessation
- 1976-04-21 DK DK179976A patent/DK179976A/da not_active Application Discontinuation
- 1976-04-21 LU LU74810A patent/LU74810A1/xx unknown
- 1976-04-22 SE SE7604669A patent/SE431980B/sv unknown
- 1976-04-22 GB GB16447/76A patent/GB1492335A/en not_active Expired
- 1976-04-22 FR FR7611953A patent/FR2308618A1/fr active Granted
- 1976-04-22 NO NO761375A patent/NO141716C/no unknown
- 1976-04-22 BE BE166372A patent/BE841008A/xx not_active IP Right Cessation
- 1976-04-22 NL NL7604301.A patent/NL166257C/xx not_active IP Right Cessation
- 1976-04-22 DD DD192464A patent/DD125345A5/xx unknown
- 1976-04-23 DE DE2617917A patent/DE2617917C3/de not_active Expired
- 1976-04-23 IE IE867/76A patent/IE43468B1/en unknown
- 1976-04-23 JP JP51045613A patent/JPS51128919A/ja active Pending

Also Published As

Publication number	Publication date
GB1492335A (en)	1977-11-16
NL166257B (nl)	1981-02-16
NO761375L (sv)	1976-10-26
BE841008A (fr)	1976-10-22
DK179976A (da)	1976-10-24
AU1311376A (en)	1977-10-27
DE2617917C3 (de)	1978-04-13
FR2308618B1 (sv)	1978-11-17
JPS51128919A (en)	1976-11-10
DE2617917A1 (de)	1976-10-28
SE7604669L (sv)	1976-10-24
SE431980B (sv)	1984-03-12
ZA762220B (en)	1977-04-27
US4020093A (en)	1977-04-26
FR2308618A1 (fr)	1976-11-19
NL166257C (nl)	1981-07-15
IT1037578B (it)	1979-11-20
IE43468L (en)	1976-10-23
ES447393A1 (es)	1977-07-01
NO141716B (no)	1980-01-21
AU502237B2 (en)	1979-07-19
NL7604301A (nl)	1976-10-26
CA1074808A (en)	1980-04-01
DD125345A5 (sv)	1977-04-13
IE43468B1 (en)	1981-03-11
LU74810A1 (sv)	1977-01-12
DE2617917B2 (de)	1977-08-18
NO141716C (no)	1980-04-30

Legal Events

Date	Code	Title	Description
1985-12-31	PL	Patent ceased

Publication	Publication Date	Title
Farthing	1950	627. Synthetic polypeptides. Part I. Synthesis of oxazolid-2: 5-diones and a new reaction of glycine
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BR122018074306B1 (pt)	2020-02-27	Método para preparar um composto de fórmula 1a
IE44472B1 (en)	1981-12-16	Prodution of aromatic urethanes
CH626335A5 (sv)	1981-11-13
JPS588380B2 (ja)	1983-02-15	有機アミン類の製造法
BRPI0910595B1 (pt)	2020-08-18	processo para a produção de composto de pirimidina
PL101177B1 (pl)	1978-12-30	Sposob wytwarzania pochodnych tiokarbaminianow
Sisler et al.	1959	Amination of tertiary amines by hydroxylamine-O-sulfonic acid
US2311046A (en)	1943-02-16	Manufacture of aromatic isocyanates
CA1226282A (en)	1987-09-01	Tricyclic derivatives of 5,6-dihydro-11h-dibenzo (b, e) azepin-6-one having pharmacological activity, and relative production methods
US4122090A (en)	1978-10-24	Cyclic esters of 3,4-dihydroxy-thiophene-1,1-dioxide compounds and 3,4-dihydroxy-cyclopentadienone compounds
EP0021641A1 (en)	1981-01-07	Process for preparing arylsulfonyl isocyanates by phosgenation of arylsulfonamides, and the products of the process and their use
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RU2711231C1 (ru)	2020-01-15	Способ получения регулятора роста растений N-(изопропоксикарбонил)-О-(4-хлорфенилкарбамоил)этаноламина
RU2264384C2 (ru)	2005-11-20	Способ получения 2- и 4-алкиламино-3-амино-5-нитробензойных кислот
US2126180A (en)	1938-08-09	Ureido n-diaryl dicarboxylic acid halides
SU825511A1 (ru)	1981-04-30	Способ получени диизоцианатов
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US3839416A (en)	1974-10-01	Trimethyl ester of carboxydithioimido-carbonic acid
JP2007503419A (ja)	2007-02-22	α−アミノ酸のウレタン保護Ｎ−無水カルボン酸の製造法
KR960007530B1 (ko)	1996-06-05	설포닐우레아 유도체의 제조방법
Dixon	1899	XXXVII.—On Lössner's benzoylethyloxysulphocarbamic acid; and the formation of pseudoureas
RU2103263C1 (ru)	1998-01-27	Способ получения замещенных n-(1,3,5-триазин-2-ил)аминокарбониларилсульфонамидов