CA3059283A1 - C5-anilinoquinazoline compounds and their use in treating cancer - Google Patents
C5-anilinoquinazoline compounds and their use in treating cancer Download PDFInfo
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- CA3059283A1 CA3059283A1 CA3059283A CA3059283A CA3059283A1 CA 3059283 A1 CA3059283 A1 CA 3059283A1 CA 3059283 A CA3059283 A CA 3059283A CA 3059283 A CA3059283 A CA 3059283A CA 3059283 A1 CA3059283 A1 CA 3059283A1
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- Prior art keywords
- compound
- triazol
- amino
- acetamide
- formula
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- 206010028980 Neoplasm Diseases 0.000 title claims description 51
- 201000011510 cancer Diseases 0.000 title claims description 45
- LKOVMZOJAULFNX-UHFFFAOYSA-N n-phenylquinazolin-5-amine Chemical class C=1C=CC2=NC=NC=C2C=1NC1=CC=CC=C1 LKOVMZOJAULFNX-UHFFFAOYSA-N 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 277
- 150000003839 salts Chemical class 0.000 claims abstract description 119
- 238000000034 method Methods 0.000 claims abstract description 30
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 10
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 95
- -1 N-(4-{[5-Fluoro-7-(2-methoxyethoxy)quinazolin-4-yl]amino}phenyl)-2-[4-(propan-yl)-1H-1,2,3-triazol-1-yl]acetamide Chemical compound 0.000 claims description 67
- 230000005855 radiation Effects 0.000 claims description 51
- 238000011282 treatment Methods 0.000 claims description 34
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 241001465754 Metazoa Species 0.000 claims description 17
- 238000002560 therapeutic procedure Methods 0.000 claims description 15
- 125000001153 fluoro group Chemical group F* 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 11
- 239000012458 free base Substances 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 239000003085 diluting agent Substances 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 5
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 5
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- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- MFPLMURQMQGFCG-UHFFFAOYSA-N 2-(4-propan-2-yltriazol-1-yl)-N-[4-[(5,6,7-trimethoxyquinazolin-4-yl)amino]phenyl]acetamide Chemical compound COC1=C(OC)C(OC)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 MFPLMURQMQGFCG-UHFFFAOYSA-N 0.000 claims 1
- FBFRRDLCELTRHJ-UHFFFAOYSA-N N-[4-[(5,7-diethoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound C(C)OC1=C2C(=NC=NC2=CC(=C1)OCC)NC1=CC=C(C=C1)NC(CN1N=NC(=C1)C(C)C)=O FBFRRDLCELTRHJ-UHFFFAOYSA-N 0.000 claims 1
- LZALBHKSKNGTHH-UHFFFAOYSA-N N-[4-[(5,7-dimethoxyquinazolin-4-yl)amino]-3-fluorophenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COC1=CC(OC)=C2C(NC3=C(F)C=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 LZALBHKSKNGTHH-UHFFFAOYSA-N 0.000 claims 1
- SRGPWBUXBAUYDE-UHFFFAOYSA-N N-[4-[(5,7-dimethoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COC1=CC(OC)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 SRGPWBUXBAUYDE-UHFFFAOYSA-N 0.000 claims 1
- ZIDCCLUJGIGJMQ-UHFFFAOYSA-N N-[4-[(5-ethoxy-7-methoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound CCOC1=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=CC(OC)=C1 ZIDCCLUJGIGJMQ-UHFFFAOYSA-N 0.000 claims 1
- GQSOEXIDXOEEPP-UHFFFAOYSA-N N-[4-[(5-fluoro-6,7-dimethoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COC1=C(OC)C(F)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 GQSOEXIDXOEEPP-UHFFFAOYSA-N 0.000 claims 1
- ZHSBZQFDAKQEPZ-UHFFFAOYSA-N N-[4-[(5-fluoro-7-methoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COC1=CC(F)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 ZHSBZQFDAKQEPZ-UHFFFAOYSA-N 0.000 claims 1
- ADVRHODTWBXWRD-UHFFFAOYSA-N N-[4-[(5-methoxy-7-propan-2-yloxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COC1=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=CC(OC(C)C)=C1 ADVRHODTWBXWRD-UHFFFAOYSA-N 0.000 claims 1
- KNIDFCMWOFTDMU-UHFFFAOYSA-N N-[4-[(7-ethoxy-5-methoxyquinazolin-4-yl)amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound CCOC1=CC(OC)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 KNIDFCMWOFTDMU-UHFFFAOYSA-N 0.000 claims 1
- HRELCAILQYPZKI-UHFFFAOYSA-N N-[4-[[5-ethoxy-7-(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound C(C)OC1=C2C(=NC=NC2=CC(=C1)OCCOC)NC1=CC=C(C=C1)NC(CN1N=NC(=C1)C(C)C)=O HRELCAILQYPZKI-UHFFFAOYSA-N 0.000 claims 1
- IIKVGFPGSYHKNK-UHFFFAOYSA-N N-[4-[[5-ethoxy-7-(oxan-4-yloxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound C(C)OC1=C2C(=NC=NC2=CC(=C1)OC1CCOCC1)NC1=CC=C(C=C1)NC(CN1N=NC(=C1)C(C)C)=O IIKVGFPGSYHKNK-UHFFFAOYSA-N 0.000 claims 1
- TWQMRFVRNFHUNB-UHFFFAOYSA-N N-[4-[[5-ethoxy-7-(oxetan-3-yloxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound C(C)OC1=C2C(=NC=NC2=CC(=C1)OC1COC1)NC1=CC=C(C=C1)NC(CN1N=NC(=C1)C(C)C)=O TWQMRFVRNFHUNB-UHFFFAOYSA-N 0.000 claims 1
- HLZBMFSNSIXJLW-HXUWFJFHSA-N N-[4-[[5-ethoxy-7-[(3R)-oxolan-3-yl]oxyquinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound CCOC1=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=CC(O[C@@H]2CCOC2)=C1 HLZBMFSNSIXJLW-HXUWFJFHSA-N 0.000 claims 1
- HLZBMFSNSIXJLW-FQEVSTJZSA-N N-[4-[[5-ethoxy-7-[(3S)-oxolan-3-yl]oxyquinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound CCOC1=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=CC(O[C@H]2CCOC2)=C1 HLZBMFSNSIXJLW-FQEVSTJZSA-N 0.000 claims 1
- FLJOFQUXYAWOPE-UHFFFAOYSA-N N-[4-[[5-fluoro-7-(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound FC1=C2C(=NC=NC2=CC(=C1)OCCOC)NC1=CC=C(C=C1)NC(CN1N=NC(=C1)C(C)C)=O FLJOFQUXYAWOPE-UHFFFAOYSA-N 0.000 claims 1
- AWHHAHZPRULJMA-UHFFFAOYSA-N N-[4-[[5-fluoro-7-(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide 4-methylbenzenesulfonic acid Chemical compound Cc1ccc(cc1)S(O)(=O)=O.COCCOc1cc(F)c2c(Nc3ccc(NC(=O)Cn4cc(nn4)C(C)C)cc3)ncnc2c1 AWHHAHZPRULJMA-UHFFFAOYSA-N 0.000 claims 1
- FMZCELDVKFMZNZ-UHFFFAOYSA-N N-[4-[[5-methoxy-7-(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-(4-propan-2-yltriazol-1-yl)acetamide Chemical compound COCCOC1=CC(OC)=C2C(NC3=CC=C(NC(=O)CN4C=C(N=N4)C(C)C)C=C3)=NC=NC2=C1 FMZCELDVKFMZNZ-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2121/00—Preparations for use in therapy
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
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| US62/490,859 | 2017-04-27 | ||
| PCT/EP2018/060798 WO2018197642A1 (en) | 2017-04-27 | 2018-04-26 | C5-anilinoquinazoline compounds and their use in treating cancer |
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| CA3059283A1 true CA3059283A1 (en) | 2018-11-01 |
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| WO2020078453A1 (en) * | 2018-10-18 | 2020-04-23 | Sinomab Bioscience Limited | Methods of treating rheumatoid arthritis |
| UY38540A (es) * | 2019-01-14 | 2020-08-31 | Pi Industries Ltd | Compuestos de fenilamidina 3-sustituida, preparación y uso |
| IL297986A (en) | 2020-05-08 | 2023-01-01 | Genmab As | Bispecific antibodies against cd3 and cd20 |
| US20240034788A1 (en) * | 2020-08-20 | 2024-02-01 | The Board Of Trustees Of The Leland Stanford Junior University | Abscopal therapy for cancer |
| MX2023002545A (es) | 2020-09-10 | 2023-03-14 | Genmab As | Anticuerpo biespecifico contra cumulo de diferenciacion 3 (cd3) y cumulo de diferenciacion 20 (cd20) en terapia de combinacion para el tratamiento de linfoma difuso de celulas b grandes. |
| CN116406293A (zh) | 2020-09-10 | 2023-07-07 | 健玛保 | 用于治疗滤泡性淋巴瘤的联合疗法中的针对cd3和cd20的双特异性抗体 |
| CN116437956A (zh) | 2020-09-10 | 2023-07-14 | 健玛保 | 用于治疗慢性淋巴细胞白血病的针对cd3和cd20的双特异性抗体 |
| CN116507363A (zh) | 2020-09-10 | 2023-07-28 | 健玛保 | 用于治疗滤泡性淋巴瘤的联合疗法中的针对cd3和cd20的双特异性抗体 |
| CA3192255A1 (en) | 2020-09-10 | 2022-03-17 | Brian Elliott | Bispecific antibody against cd3 and cd20 in combination therapy for treating diffuse large b-cell lymphoma |
| KR20240117094A (ko) * | 2021-12-09 | 2024-07-31 | 데시페라 파마슈티칼스, 엘엘씨. | Kit 키나아제 억제제로서의 헤테로시클릭 화합물 |
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| WO2014181287A1 (en) | 2013-05-09 | 2014-11-13 | Piramal Enterprises Limited | Heterocyclyl compounds and uses thereof |
| CN104130200B (zh) | 2014-07-01 | 2016-04-20 | 中山大学 | 一种2-取代苯基-4-芳胺基喹唑啉衍生物及其制备方法和应用 |
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| JP7117323B2 (ja) | 2017-04-27 | 2022-08-12 | アストラゼネカ・アクチエボラーグ | フェノキシキナゾリン化合物及び癌の処置におけるそれらの使用 |
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2018
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- 2018-04-26 EP EP18721348.3A patent/EP3615522B1/en active Active
- 2018-04-26 JP JP2019557764A patent/JP7128204B2/ja active Active
- 2018-04-26 MX MX2019012847A patent/MX389244B/es unknown
- 2018-04-26 CA CA3059283A patent/CA3059283A1/en active Pending
- 2018-04-26 WO PCT/EP2018/060798 patent/WO2018197642A1/en not_active Ceased
- 2018-04-26 CN CN201880027620.0A patent/CN110573505B/zh active Active
- 2018-04-26 RU RU2019136279A patent/RU2769694C2/ru active
- 2018-04-26 TW TW107114297A patent/TWI774758B/zh active
- 2018-04-26 US US15/963,122 patent/US10273227B2/en active Active
- 2018-04-26 KR KR1020197034070A patent/KR102603153B1/ko active Active
- 2018-04-26 AU AU2018259078A patent/AU2018259078B2/en active Active
- 2018-04-27 AR ARP180101102A patent/AR111494A1/es unknown
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2019
- 2019-03-05 US US16/292,817 patent/US10829479B2/en active Active
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| WO2018197642A1 (en) | 2018-11-01 |
| BR112019022229A2 (pt) | 2020-05-12 |
| AR111494A1 (es) | 2019-07-17 |
| CN110573505B (zh) | 2023-04-11 |
| MX389244B (es) | 2025-03-20 |
| US10273227B2 (en) | 2019-04-30 |
| RU2019136279A3 (enExample) | 2021-05-31 |
| US10829479B2 (en) | 2020-11-10 |
| TW201904960A (zh) | 2019-02-01 |
| CN110573505A (zh) | 2019-12-13 |
| US20180312490A1 (en) | 2018-11-01 |
| KR20190141203A (ko) | 2019-12-23 |
| ES2888298T3 (es) | 2022-01-03 |
| AU2018259078B2 (en) | 2021-10-07 |
| KR102603153B1 (ko) | 2023-11-15 |
| JP7128204B2 (ja) | 2022-08-30 |
| US20190263787A1 (en) | 2019-08-29 |
| TWI774758B (zh) | 2022-08-21 |
| RU2019136279A (ru) | 2021-05-27 |
| EP3615522A1 (en) | 2020-03-04 |
| MX2019012847A (es) | 2022-01-07 |
| JP2020517677A (ja) | 2020-06-18 |
| EP3615522B1 (en) | 2021-08-04 |
| RU2769694C2 (ru) | 2022-04-05 |
| AU2018259078A1 (en) | 2019-10-17 |
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