CZ365392A3 - Sulfonimidamide derivative, process for preparing thereof and a pharmaceutical preparation in which it is contained - Google Patents
Sulfonimidamide derivative, process for preparing thereof and a pharmaceutical preparation in which it is contained Download PDFInfo
- Publication number
- CZ365392A3 CZ365392A3 CS923653A CS365392A CZ365392A3 CZ 365392 A3 CZ365392 A3 CZ 365392A3 CS 923653 A CS923653 A CS 923653A CS 365392 A CS365392 A CS 365392A CZ 365392 A3 CZ365392 A3 CZ 365392A3
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- CZ
- Czechia
- Prior art keywords
- group
- carbonyl
- methyl
- hydrogen
- formula
- Prior art date
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- 239000000825 pharmaceutical preparation Substances 0.000 title description 5
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 58
- 239000000460 chlorine Substances 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims abstract description 35
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 24
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 18
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 17
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000002246 antineoplastic agent Substances 0.000 claims abstract description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 6
- 230000008569 process Effects 0.000 claims abstract description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- 229940034982 antineoplastic agent Drugs 0.000 claims abstract description 4
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 3
- 239000011630 iodine Chemical group 0.000 claims abstract description 3
- 206010028980 Neoplasm Diseases 0.000 claims description 43
- -1 group Substances 0.000 claims description 42
- 229910052739 hydrogen Inorganic materials 0.000 claims description 39
- 239000001257 hydrogen Substances 0.000 claims description 29
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 23
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 20
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 20
- 239000004480 active ingredient Substances 0.000 claims description 19
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 19
- 150000002431 hydrogen Chemical class 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- INOGLHRUEYDAHX-UHFFFAOYSA-N 1-chlorobenzotriazole Chemical compound C1=CC=C2N(Cl)N=NC2=C1 INOGLHRUEYDAHX-UHFFFAOYSA-N 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 201000011510 cancer Diseases 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
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- 238000006243 chemical reaction Methods 0.000 claims description 5
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- 239000007800 oxidant agent Substances 0.000 claims description 4
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 3
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- 239000003085 diluting agent Substances 0.000 claims description 3
- BTCCJSNEWMLWOE-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[(3,4,5-trimethylphenyl)sulfonimidoyl]urea Chemical compound CC1=C(C)C(C)=CC(S(=N)(=O)NC(=O)NC=2C=CC(Cl)=CC=2)=C1 BTCCJSNEWMLWOE-UHFFFAOYSA-N 0.000 claims description 2
- JVUYQHDSVZWYKP-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[n-ethyl-s-(4-methylphenyl)sulfonimidoyl]urea Chemical compound C=1C=C(C)C=CC=1S(=O)(=NCC)NC(=O)NC1=CC=C(Cl)C=C1 JVUYQHDSVZWYKP-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
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- 239000003937 drug carrier Substances 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- YOIDHZBOHMNTNP-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-(4-methylphenyl)sulfonylurea Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)NC1=CC=C(Cl)C=C1 YOIDHZBOHMNTNP-UHFFFAOYSA-N 0.000 claims 1
- CSWDCNAHHKISFH-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[(4-chlorophenyl)sulfonimidoyl]urea Chemical compound C1=CC(Cl)=CC=C1NC(=O)NS(=N)(=O)C1=CC=C(Cl)C=C1 CSWDCNAHHKISFH-UHFFFAOYSA-N 0.000 claims 1
- QUFVCQSBHRJKFG-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[s-(3,4-dimethylphenyl)-n-methylsulfonimidoyl]urea Chemical compound C=1C=C(C)C(C)=CC=1S(=O)(NC)=NC(=O)NC1=CC=C(Cl)C=C1 QUFVCQSBHRJKFG-UHFFFAOYSA-N 0.000 claims 1
- MKZRXMVJTBPROZ-UHFFFAOYSA-N 1-(aminosulfonimidoyl)-2-methylbenzene Chemical compound CC1=CC=CC=C1S(N)(=N)=O MKZRXMVJTBPROZ-UHFFFAOYSA-N 0.000 claims 1
- 241001556567 Acanthamoeba polyphaga mimivirus Species 0.000 claims 1
- 230000000118 anti-neoplastic effect Effects 0.000 claims 1
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- 238000009472 formulation Methods 0.000 abstract description 5
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
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- 239000000047 product Substances 0.000 description 167
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- 238000004458 analytical method Methods 0.000 description 99
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- 238000005481 NMR spectroscopy Methods 0.000 description 69
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 60
- 235000019439 ethyl acetate Nutrition 0.000 description 55
- 238000000434 field desorption mass spectrometry Methods 0.000 description 55
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- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 42
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 30
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- 229910052760 oxygen Inorganic materials 0.000 description 27
- 239000007787 solid Substances 0.000 description 27
- 239000000243 solution Substances 0.000 description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- 238000001953 recrystallisation Methods 0.000 description 17
- 238000003818 flash chromatography Methods 0.000 description 16
- 229910052757 nitrogen Inorganic materials 0.000 description 16
- IXZDIALLLMRYOU-UHFFFAOYSA-N tert-butyl hypochlorite Chemical compound CC(C)(C)OCl IXZDIALLLMRYOU-UHFFFAOYSA-N 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- DOQQTKLDEQSKIE-UHFFFAOYSA-N silver;isocyanate Chemical compound [Ag+].[N-]=C=O DOQQTKLDEQSKIE-UHFFFAOYSA-N 0.000 description 15
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- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
- 239000012043 crude product Substances 0.000 description 12
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
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- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 7
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
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- 239000000375 suspending agent Substances 0.000 description 1
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- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/10—Compounds containing sulfur atoms doubly-bound to nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81225991A | 1991-12-20 | 1991-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ365392A3 true CZ365392A3 (en) | 1993-10-13 |
Family
ID=25209033
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS923653A CZ365392A3 (en) | 1991-12-20 | 1992-12-14 | Sulfonimidamide derivative, process for preparing thereof and a pharmaceutical preparation in which it is contained |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0552553B1 (https=) |
| JP (1) | JP3202373B2 (https=) |
| AU (1) | AU654069B2 (https=) |
| BR (1) | BR9205020A (https=) |
| CA (1) | CA2085297A1 (https=) |
| CZ (1) | CZ365392A3 (https=) |
| DE (1) | DE69221114T2 (https=) |
| ES (1) | ES2104857T3 (https=) |
| FI (1) | FI925693A7 (https=) |
| HU (1) | HUT65746A (https=) |
| IL (1) | IL104088A0 (https=) |
| MX (1) | MX9207264A (https=) |
| NO (1) | NO924848L (https=) |
| NZ (1) | NZ245458A (https=) |
| TW (1) | TW221049B (https=) |
| YU (1) | YU107692A (https=) |
| ZA (1) | ZA929699B (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS65492B1 (sr) * | 2017-07-24 | 2024-05-31 | Novartis Ag | Jedinjenja i kompozicije za lečenje stanja povezanih sa aktivnošću nlrp |
| CN111094242B (zh) * | 2017-07-24 | 2024-02-09 | 诺华股份有限公司 | 用于治疗与nlrp活性相关的病症的化合物和组合物 |
| US11623922B2 (en) | 2017-10-03 | 2023-04-11 | Inflazome Limited | Compounds |
| CN112654350A (zh) * | 2018-07-03 | 2021-04-13 | 诺华股份有限公司 | 使用nlrp3拮抗剂治疗对tnf抑制剂有抗性的受试者或针对所述患者选择治疗的方法 |
| EP3880666B1 (en) | 2018-11-13 | 2023-06-28 | Novartis AG | Compounds and compositions for treating conditions associated with nlrp activity |
| CN113015730A (zh) | 2018-11-13 | 2021-06-22 | 诺华股份有限公司 | 用于治疗与nlrp活性相关的病症的化合物和组合物 |
| US20230059136A1 (en) * | 2018-11-16 | 2023-02-23 | Novartis Ag | The compounds and compositions for treating conditions associated with nlrp activity |
| WO2021002887A1 (en) * | 2019-07-02 | 2021-01-07 | Novartis Inflammasome Research, Inc. | Gut-targeted nlrp3 antagonists and their use in therapy |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4666506A (en) | 1984-08-08 | 1987-05-19 | E. I. Du Pont De Nemours And Company | Herbicidal pyrimidines |
| IL83215A (en) * | 1986-07-23 | 1991-12-15 | Lilly Co Eli | Synthesis of bicyclic heteroaromatic sulfonyl chlorides |
| US5187189A (en) * | 1991-01-22 | 1993-02-16 | American Home Products Corporation | S-aminoalkyl-s-arylsulfoximines as antiarrhythmic agents |
| US5140026A (en) * | 1991-05-09 | 1992-08-18 | A. H. Robins Company, Incorporated | N-aminoalkyl-S-aryl-S-alkyl (or substituted alkyl) sulfoximines as antiarrhythmic agents |
-
1992
- 1992-12-14 TW TW081109989A patent/TW221049B/zh active
- 1992-12-14 ZA ZA929699A patent/ZA929699B/xx unknown
- 1992-12-14 NZ NZ245458A patent/NZ245458A/en unknown
- 1992-12-14 CZ CS923653A patent/CZ365392A3/cs unknown
- 1992-12-14 CA CA002085297A patent/CA2085297A1/en not_active Abandoned
- 1992-12-14 IL IL104088A patent/IL104088A0/xx unknown
- 1992-12-15 AU AU30181/92A patent/AU654069B2/en not_active Ceased
- 1992-12-15 HU HU9203971A patent/HUT65746A/hu unknown
- 1992-12-15 ES ES92311447T patent/ES2104857T3/es not_active Expired - Lifetime
- 1992-12-15 EP EP92311447A patent/EP0552553B1/en not_active Expired - Lifetime
- 1992-12-15 NO NO92924848A patent/NO924848L/no unknown
- 1992-12-15 FI FI925693A patent/FI925693A7/fi not_active Application Discontinuation
- 1992-12-15 MX MX9207264A patent/MX9207264A/es unknown
- 1992-12-15 DE DE69221114T patent/DE69221114T2/de not_active Expired - Fee Related
- 1992-12-15 BR BR9205020A patent/BR9205020A/pt not_active Application Discontinuation
- 1992-12-16 YU YU107692A patent/YU107692A/sh unknown
- 1992-12-16 JP JP33625392A patent/JP3202373B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2085297A1 (en) | 1993-06-21 |
| NZ245458A (en) | 1995-04-27 |
| NO924848L (no) | 1993-06-21 |
| EP0552553B1 (en) | 1997-07-23 |
| JPH05345756A (ja) | 1993-12-27 |
| EP0552553A1 (en) | 1993-07-28 |
| AU654069B2 (en) | 1994-10-20 |
| MX9207264A (es) | 1993-12-01 |
| BR9205020A (pt) | 1993-06-22 |
| NO924848D0 (no) | 1992-12-15 |
| HUT65746A (en) | 1994-07-28 |
| YU107692A (sh) | 1995-12-04 |
| FI925693A7 (fi) | 1993-06-21 |
| DE69221114D1 (de) | 1997-08-28 |
| JP3202373B2 (ja) | 2001-08-27 |
| TW221049B (https=) | 1994-02-11 |
| DE69221114T2 (de) | 1997-12-11 |
| AU3018192A (en) | 1993-06-24 |
| ES2104857T3 (es) | 1997-10-16 |
| HU9203971D0 (en) | 1993-04-28 |
| FI925693A0 (fi) | 1992-12-15 |
| IL104088A0 (en) | 1993-05-13 |
| ZA929699B (en) | 1994-06-14 |
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