JP7038063B2 - ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 - Google Patents
ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 Download PDFInfo
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- JP7038063B2 JP7038063B2 JP2018552683A JP2018552683A JP7038063B2 JP 7038063 B2 JP7038063 B2 JP 7038063B2 JP 2018552683 A JP2018552683 A JP 2018552683A JP 2018552683 A JP2018552683 A JP 2018552683A JP 7038063 B2 JP7038063 B2 JP 7038063B2
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- GDQXXUPADGSRIR-HNNXBMFYSA-N Cc([n]1nc2)cc(-c3cnccc3C(F)(F)F)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3cnccc3C(F)(F)F)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O GDQXXUPADGSRIR-HNNXBMFYSA-N 0.000 description 1
- BDIOTSJMSUDGPZ-ZDUSSCGKSA-N Cc([n]1nc2)cc(-c3n[o]cc3)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3n[o]cc3)nc1c2C(N[C@@H](C1CC1)C(F)(F)F)=O BDIOTSJMSUDGPZ-ZDUSSCGKSA-N 0.000 description 1
- BACWZIINSOXLMD-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3nc(-c4ncccn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(-c3nc(-c4ncccn4)ccc3)nc1c2C(NC(C1CC1)C(F)(F)F)=O BACWZIINSOXLMD-UHFFFAOYSA-N 0.000 description 1
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- YUVGSEDLSFKSSE-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc(nc1)ccc1-c1ccc[o]1)=O Chemical compound Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc(nc1)ccc1-c1ccc[o]1)=O YUVGSEDLSFKSSE-UHFFFAOYSA-N 0.000 description 1
- MYBMXMBXWQFZDR-UHFFFAOYSA-N Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc1ccc(CCC2)c2c1)=O Chemical compound Cc([n]1nc2)cc(-c3ncccc3)nc1c2C(Nc1ccc(CCC2)c2c1)=O MYBMXMBXWQFZDR-UHFFFAOYSA-N 0.000 description 1
- KYJILWPHEKJSGM-UHFFFAOYSA-N Cc([n]1nc2)cc(N(CCN3CC(F)(F)F)C3=O)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([n]1nc2)cc(N(CCN3CC(F)(F)F)C3=O)nc1c2C(NC(C1CC1)C(F)(F)F)=O KYJILWPHEKJSGM-UHFFFAOYSA-N 0.000 description 1
- RUTPHOUZHZTUGE-UHFFFAOYSA-N Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(N=C)=O Chemical compound Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(N=C)=O RUTPHOUZHZTUGE-UHFFFAOYSA-N 0.000 description 1
- GSRKHRSALPOTBP-UHFFFAOYSA-N Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc([o]c(C#N)c1)c1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O GSRKHRSALPOTBP-UHFFFAOYSA-N 0.000 description 1
- PHGXUFPYCAWEHK-UHFFFAOYSA-N Cc(cccn1)c1F Chemical compound Cc(cccn1)c1F PHGXUFPYCAWEHK-UHFFFAOYSA-N 0.000 description 1
- WATJDHQAPWIPNM-CQSZACIVSA-N Cc1c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]nc1 Chemical compound Cc1c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]nc1 WATJDHQAPWIPNM-CQSZACIVSA-N 0.000 description 1
- OKHCIUYTCGNFHB-UHFFFAOYSA-N Cc1c[o]nc1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O Chemical compound Cc1c[o]nc1-c(cc(C)[n]1nc2)nc1c2C(NC(C1CC1)C(F)(F)F)=O OKHCIUYTCGNFHB-UHFFFAOYSA-N 0.000 description 1
- TXOHMSSZMJQZAX-CQSZACIVSA-N Cc1cc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)n[o]1 Chemical compound Cc1cc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)n[o]1 TXOHMSSZMJQZAX-CQSZACIVSA-N 0.000 description 1
- QLHCLNAQULRANK-UHFFFAOYSA-N Cc1cc(C#N)c(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1cc(C#N)c(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 QLHCLNAQULRANK-UHFFFAOYSA-N 0.000 description 1
- UDMNVTJFUISBFD-UHFFFAOYSA-N Cc1cccc(F)n1 Chemical compound Cc1cccc(F)n1 UDMNVTJFUISBFD-UHFFFAOYSA-N 0.000 description 1
- AZFSUHYOECXKOT-CQSZACIVSA-N Cc1n[o]c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)c1 Chemical compound Cc1n[o]c(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)c1 AZFSUHYOECXKOT-CQSZACIVSA-N 0.000 description 1
- OZQVZLAMNDAUCF-UHFFFAOYSA-N Cc1nc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)c[o]1 Chemical compound Cc1nc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)c[o]1 OZQVZLAMNDAUCF-UHFFFAOYSA-N 0.000 description 1
- KAHDUHPHARNQFY-UHFFFAOYSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N=C)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N=C)=O)[o]1 KAHDUHPHARNQFY-UHFFFAOYSA-N 0.000 description 1
- VWIIAOGWLUPWRF-UHFFFAOYSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(NC(C2CC2)C(F)(F)F)=O)[o]1 VWIIAOGWLUPWRF-UHFFFAOYSA-N 0.000 description 1
- VWIIAOGWLUPWRF-CQSZACIVSA-N Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]1 Chemical compound Cc1ncc(-c(cc(C)[n]2nc3)nc2c3C(N[C@H](C2CC2)C(F)(F)F)=O)[o]1 VWIIAOGWLUPWRF-CQSZACIVSA-N 0.000 description 1
- HDBGZXSGXLMEOO-UHFFFAOYSA-N FC(CC1[IH]CC1)(F)F Chemical compound FC(CC1[IH]CC1)(F)F HDBGZXSGXLMEOO-UHFFFAOYSA-N 0.000 description 1
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- JPTMBILBPYBOFL-UHFFFAOYSA-N NC1=CC=CC=[I]1 Chemical compound NC1=CC=CC=[I]1 JPTMBILBPYBOFL-UHFFFAOYSA-N 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N O=C1NCCN1 Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
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- A61P27/06—Antiglaucoma agents or miotics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- Pregnancy & Childbirth (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662318929P | 2016-04-06 | 2016-04-06 | |
| US62/318,929 | 2016-04-06 | ||
| PCT/US2017/026280 WO2017176960A1 (en) | 2016-04-06 | 2017-04-06 | Pyrazolo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
Publications (3)
| Publication Number | Publication Date |
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| JP2019510790A JP2019510790A (ja) | 2019-04-18 |
| JP2019510790A5 JP2019510790A5 (enExample) | 2021-11-04 |
| JP7038063B2 true JP7038063B2 (ja) | 2022-03-17 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2018552683A Expired - Fee Related JP7038063B2 (ja) | 2016-04-06 | 2017-04-06 | ピラゾロ[1,5-a]ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用 |
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| Country | Link |
|---|---|
| US (4) | US11192892B2 (enExample) |
| EP (1) | EP3440080A4 (enExample) |
| JP (1) | JP7038063B2 (enExample) |
| KR (2) | KR20180133461A (enExample) |
| CN (1) | CN109311887B (enExample) |
| AU (1) | AU2017246455B2 (enExample) |
| BR (1) | BR112018070586A8 (enExample) |
| CA (1) | CA3020287A1 (enExample) |
| IL (1) | IL262177B (enExample) |
| MX (1) | MX2018012211A (enExample) |
| SG (1) | SG11201808830YA (enExample) |
| WO (1) | WO2017176960A1 (enExample) |
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| WO2016073889A1 (en) | 2014-11-06 | 2016-05-12 | Lysosomal Therapeutics Inc. | Substituted imidazo[1,5-a]pyrimidines and their use in the treatment of medical disorders |
| CN107001379B (zh) | 2014-11-06 | 2022-11-01 | Bial研发投资股份有限公司 | 取代的吡唑并[1,5-a]嘧啶以及它们在治疗医学障碍中的用途 |
| AU2015342883B2 (en) | 2014-11-06 | 2020-07-02 | Bial - R&D Investments, S.A. | Substituted pyrrolo(1,2-a)pyrimidines and their use in the treatment of medical disorders |
| US10787454B2 (en) | 2016-04-06 | 2020-09-29 | BIAL—BioTech Investments, Inc. | Imidazo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| WO2017176962A1 (en) | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics, Inc. | Pyrrolo[1,2-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| WO2017176960A1 (en) | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics Inc. | Pyrazolo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| WO2017192931A1 (en) | 2016-05-05 | 2017-11-09 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMDAZO[1,2-α]PYRIDINES, SUBSTITUTED IMIDAZO[1,2-α]PYRAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
| MX389579B (es) | 2016-05-05 | 2025-03-20 | Bial R&D Invest S A | IMIDAZO[1,2-b]PIRIDAZINAS SUSTITUIDAS, IMIDAZO[1,5-b]PIRIDAZINAS SUSTITUIDAS, COMPUESTOS RELACIONADOS Y SU USO EN EL TRATAMIENTO DE TRASTORNOS MÉDICOS |
| CN110698484B (zh) * | 2019-06-05 | 2021-11-05 | 陕西理工大学 | 含吡唑并[1,5-a]嘧啶的衍生物、药用组合物及应用 |
| CN115108972A (zh) * | 2022-08-29 | 2022-09-27 | 北京迪泰医药科技有限公司 | 一种2-甲基-3-氟-5-溴吡啶的合成方法 |
| WO2025014639A2 (en) * | 2023-07-07 | 2025-01-16 | The Johns Hopkins University | Neutral sphingomyelinase inhibitors |
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| IL262177A (en) | 2018-11-29 |
| AU2017246455A1 (en) | 2018-10-25 |
| KR20180133461A (ko) | 2018-12-14 |
| US20230098494A1 (en) | 2023-03-30 |
| EP3440080A4 (en) | 2020-01-22 |
| RU2018138688A (ru) | 2020-05-19 |
| US20190330213A1 (en) | 2019-10-31 |
| CA3020287A1 (en) | 2017-10-12 |
| BR112018070586A2 (pt) | 2019-02-05 |
| SG11201808830YA (en) | 2018-11-29 |
| US20200017507A1 (en) | 2020-01-16 |
| BR112018070586A8 (pt) | 2023-03-14 |
| EP3440080A1 (en) | 2019-02-13 |
| CN109311887A (zh) | 2019-02-05 |
| RU2018138688A3 (enExample) | 2020-08-31 |
| WO2017176960A1 (en) | 2017-10-12 |
| US20170349598A1 (en) | 2017-12-07 |
| AU2017246455B2 (en) | 2021-09-30 |
| MX2018012211A (es) | 2019-03-28 |
| KR20230104752A (ko) | 2023-07-10 |
| CN109311887B (zh) | 2022-09-13 |
| US9840510B1 (en) | 2017-12-12 |
| US11192892B2 (en) | 2021-12-07 |
| IL262177B (en) | 2022-06-01 |
| JP2019510790A (ja) | 2019-04-18 |
| US12116369B2 (en) | 2024-10-15 |
| US10934298B2 (en) | 2021-03-02 |
| KR20230104752A9 (ko) | 2024-11-15 |
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