CN102574860A - 吡咯并[2,3-d]嘧啶化合物 - Google Patents
吡咯并[2,3-d]嘧啶化合物 Download PDFInfo
- Publication number
- CN102574860A CN102574860A CN2010800461239A CN201080046123A CN102574860A CN 102574860 A CN102574860 A CN 102574860A CN 2010800461239 A CN2010800461239 A CN 2010800461239A CN 201080046123 A CN201080046123 A CN 201080046123A CN 102574860 A CN102574860 A CN 102574860A
- Authority
- CN
- China
- Prior art keywords
- methyl
- alkyl
- hydrogen
- amino
- pyrrolo
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 0 *S(c1ccccc1)(=O)=O Chemical compound *S(c1ccccc1)(=O)=O 0.000 description 7
- DFVBZOPVGGDURA-BZUAXINKSA-N CN([C@H]1CC[C@H](CS(N(CCC2)C[C@@H]2O)(=O)=O)CC1)c1c(cc[nH]2)c2ncn1 Chemical compound CN([C@H]1CC[C@H](CS(N(CCC2)C[C@@H]2O)(=O)=O)CC1)c1c(cc[nH]2)c2ncn1 DFVBZOPVGGDURA-BZUAXINKSA-N 0.000 description 2
- RJSZFSOFYVMDIC-UHFFFAOYSA-N CC(C)(C)OC(N(C)C)=O Chemical compound CC(C)(C)OC(N(C)C)=O RJSZFSOFYVMDIC-UHFFFAOYSA-N 0.000 description 1
- ZZUBWARPJPCIFH-UHFFFAOYSA-N CCOCc1cnccc1 Chemical compound CCOCc1cnccc1 ZZUBWARPJPCIFH-UHFFFAOYSA-N 0.000 description 1
- UWWCZZMOTBWUAB-UHFFFAOYSA-N CCOc1cc(F)ccc1 Chemical compound CCOc1cc(F)ccc1 UWWCZZMOTBWUAB-UHFFFAOYSA-N 0.000 description 1
- FNTBXHXRHAFYJT-UHFFFAOYSA-N CCSc1ncccc1 Chemical compound CCSc1ncccc1 FNTBXHXRHAFYJT-UHFFFAOYSA-N 0.000 description 1
- FLNMQGISZVYIIK-UHFFFAOYSA-N CC[n]1nccc1 Chemical compound CC[n]1nccc1 FLNMQGISZVYIIK-UHFFFAOYSA-N 0.000 description 1
- QKAVREGFSUASSA-UHFFFAOYSA-N CCc1ccc(C)nn1 Chemical compound CCc1ccc(C)nn1 QKAVREGFSUASSA-UHFFFAOYSA-N 0.000 description 1
- IWLCZDAXJKCXCB-UHFFFAOYSA-N CCc1ccc(COCC)nc1 Chemical compound CCc1ccc(COCC)nc1 IWLCZDAXJKCXCB-UHFFFAOYSA-N 0.000 description 1
- RILVNLMOTMFTMQ-UHFFFAOYSA-N CCc1ncccn1 Chemical compound CCc1ncccn1 RILVNLMOTMFTMQ-UHFFFAOYSA-N 0.000 description 1
- AXWBJJJQRJBTMI-UHFFFAOYSA-N CNc1c(cc[nH]2)c2ncn1 Chemical compound CNc1c(cc[nH]2)c2ncn1 AXWBJJJQRJBTMI-UHFFFAOYSA-N 0.000 description 1
- CFLBWBNKHWRLND-UHFFFAOYSA-N COCC(N1CCCC1)=O Chemical compound COCC(N1CCCC1)=O CFLBWBNKHWRLND-UHFFFAOYSA-N 0.000 description 1
- KXJNMUVDHMKDFH-UHFFFAOYSA-N COc1ccccc1CS(C)(=O)=O Chemical compound COc1ccccc1CS(C)(=O)=O KXJNMUVDHMKDFH-UHFFFAOYSA-N 0.000 description 1
- IFGILWAJARXQMW-UHFFFAOYSA-N CS(Cc1ccccc1)(O)=O Chemical compound CS(Cc1ccccc1)(O)=O IFGILWAJARXQMW-UHFFFAOYSA-N 0.000 description 1
- RLOXRDZNXQYPSL-UEJVZZJDSA-N C[C@@H](CC(CC1)C(OC)=O)C1NC Chemical compound C[C@@H](CC(CC1)C(OC)=O)C1NC RLOXRDZNXQYPSL-UEJVZZJDSA-N 0.000 description 1
- ODABGSCQQBWPJE-VORVDWIASA-N C[C@@H](C[C@H](CC1)C(OC)=O)C1N(C)C(c1ccccc1C(OC)=O)=O Chemical compound C[C@@H](C[C@H](CC1)C(OC)=O)C1N(C)C(c1ccccc1C(OC)=O)=O ODABGSCQQBWPJE-VORVDWIASA-N 0.000 description 1
- DWJRXJWZPSIJPZ-OUCADQQQSA-N C[C@@H](C[C@H](CS(NC)(=O)=O)CC1)[C@@H]1N(C)c1c(cc[nH]2)c2ncn1 Chemical compound C[C@@H](C[C@H](CS(NC)(=O)=O)CC1)[C@@H]1N(C)c1c(cc[nH]2)c2ncn1 DWJRXJWZPSIJPZ-OUCADQQQSA-N 0.000 description 1
- MQACXCCKFOCMDR-UHFFFAOYSA-N Cc(cc(cc1)C(OC)=O)c1N(C)C(OCc1ccccc1)=O Chemical compound Cc(cc(cc1)C(OC)=O)c1N(C)C(OCc1ccccc1)=O MQACXCCKFOCMDR-UHFFFAOYSA-N 0.000 description 1
- OHJXSEODCOULCR-UHFFFAOYSA-N Cc(cc1)ccc1[S](=O)=O Chemical compound Cc(cc1)ccc1[S](=O)=O OHJXSEODCOULCR-UHFFFAOYSA-N 0.000 description 1
- MMZYCBHLNZVROM-UHFFFAOYSA-N Cc(cccc1)c1F Chemical compound Cc(cccc1)c1F MMZYCBHLNZVROM-UHFFFAOYSA-N 0.000 description 1
- DTFKRVXLBCAIOZ-UHFFFAOYSA-N Cc(cccc1)c1OC Chemical compound Cc(cccc1)c1OC DTFKRVXLBCAIOZ-UHFFFAOYSA-N 0.000 description 1
- UBKKNWJGYLSDSJ-UHFFFAOYSA-N Cc(nccc1)c1C#N Chemical compound Cc(nccc1)c1C#N UBKKNWJGYLSDSJ-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N Cc1ccccn1 Chemical compound Cc1ccccn1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- JDEQYBVUGWGTFF-UHFFFAOYSA-N Cc1nc(CS(C)(=O)=O)n[o]1 Chemical compound Cc1nc(CS(C)(=O)=O)n[o]1 JDEQYBVUGWGTFF-UHFFFAOYSA-N 0.000 description 1
- LNJMHEJAYSYZKK-UHFFFAOYSA-N Cc1ncccn1 Chemical compound Cc1ncccn1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 1
- YVDWFZIVIIKYBQ-UHFFFAOYSA-N Cc1nnc(C)[o]1 Chemical compound Cc1nnc(C)[o]1 YVDWFZIVIIKYBQ-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
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P11/00—Drugs for disorders of the respiratory system
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/04—Artificial tears; Irrigation solutions
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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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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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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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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- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Ophthalmology & Optometry (AREA)
- Virology (AREA)
- Reproductive Health (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25203909P | 2009-10-15 | 2009-10-15 | |
| US61/252,039 | 2009-10-15 | ||
| PCT/IB2010/054447 WO2011045702A1 (en) | 2009-10-15 | 2010-10-01 | Pyrrolo[2,3-d] pyrimidine compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102574860A true CN102574860A (zh) | 2012-07-11 |
Family
ID=43413616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2010800461239A Pending CN102574860A (zh) | 2009-10-15 | 2010-10-01 | 吡咯并[2,3-d]嘧啶化合物 |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US8633206B2 (enExample) |
| EP (1) | EP2488524B1 (enExample) |
| JP (1) | JP5629324B2 (enExample) |
| KR (1) | KR20120083452A (enExample) |
| CN (1) | CN102574860A (enExample) |
| AP (1) | AP2012006192A0 (enExample) |
| AR (1) | AR078635A1 (enExample) |
| AU (1) | AU2010308028A1 (enExample) |
| CA (1) | CA2776028C (enExample) |
| CL (1) | CL2012000795A1 (enExample) |
| CO (1) | CO6531451A2 (enExample) |
| CR (1) | CR20120164A (enExample) |
| CU (1) | CU20120059A7 (enExample) |
| DO (1) | DOP2012000080A (enExample) |
| EA (1) | EA201290147A1 (enExample) |
| EC (1) | ECSP12011855A (enExample) |
| ES (1) | ES2426407T3 (enExample) |
| IL (1) | IL218802A0 (enExample) |
| IN (1) | IN2012DN02577A (enExample) |
| MA (1) | MA33670B1 (enExample) |
| MX (1) | MX2012004379A (enExample) |
| NI (1) | NI201200053A (enExample) |
| PE (1) | PE20121077A1 (enExample) |
| PH (1) | PH12012500583A1 (enExample) |
| TN (1) | TN2012000146A1 (enExample) |
| TW (1) | TWI398444B (enExample) |
| UY (1) | UY32947A (enExample) |
| WO (1) | WO2011045702A1 (enExample) |
| ZA (1) | ZA201202718B (enExample) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103896946A (zh) * | 2012-12-28 | 2014-07-02 | 浙江导明医药科技有限公司 | 用于预防及治疗多种自身免疫疾病的新化合物 |
| CN105164133A (zh) * | 2013-05-02 | 2015-12-16 | 豪夫迈·罗氏有限公司 | 作为CB2受体激动剂的吡咯并[2,3-d]嘧啶衍生物 |
| CN105008362B (zh) * | 2013-02-22 | 2017-06-06 | 辉瑞大药厂 | 作为詹纳斯相关激酶(jak)抑制剂的吡咯并[2,3‑d]嘧啶衍生物 |
| CN111499641A (zh) * | 2019-01-30 | 2020-08-07 | 格格巫(珠海)生物科技有限公司 | 一种jak抑制剂及其制备方法 |
| CN114025758A (zh) * | 2019-07-01 | 2022-02-08 | 钱立刚 | P2x7r拮抗剂 |
| CN114761011A (zh) * | 2019-08-26 | 2022-07-15 | 肯沃斯公司 | 用作jak1抑制剂的取代的(7h-吡咯并[2,3-d]嘧啶-4-基)氨基化合物 |
| CN115246833A (zh) * | 2021-04-27 | 2022-10-28 | 洛阳惠中兽药有限公司 | 一种奥拉替尼化合物及其中间体化合物的制备方法 |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9394333B2 (en) | 2008-12-02 | 2016-07-19 | Wave Life Sciences Japan | Method for the synthesis of phosphorus atom modified nucleic acids |
| BRPI1013559A2 (pt) | 2009-03-23 | 2016-04-12 | Glenmark Pharmaceuticals Sa | compostos, composição farmacêutica, método de tratamento de doença ou condição associada à função trpa1 e respectivos usos |
| EP2411395B1 (en) | 2009-03-23 | 2013-05-29 | Glenmark Pharmaceuticals S.A. | Furopyrimidinedione derivatives as trpa1 modulators |
| MX342945B (es) | 2009-07-06 | 2016-10-18 | Ontorii Inc * | Profármacos de ácido nucleico novedosos y métodos de uso de los mismos. |
| TW201111385A (en) * | 2009-08-27 | 2011-04-01 | Biocryst Pharm Inc | Heterocyclic compounds as janus kinase inhibitors |
| WO2011075334A1 (en) * | 2009-12-18 | 2011-06-23 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine compounds |
| DK2620428T3 (da) * | 2010-09-24 | 2019-07-01 | Wave Life Sciences Ltd | Asymmetrisk hjælpegruppe |
| US9605019B2 (en) | 2011-07-19 | 2017-03-28 | Wave Life Sciences Ltd. | Methods for the synthesis of functionalized nucleic acids |
| PH12013502670A1 (en) | 2011-08-12 | 2016-07-29 | Nissan Chemical Ind Ltd | Tricyclic heterocyclic compounds and jak inhibitors |
| SG11201500243WA (en) | 2012-07-13 | 2015-04-29 | Shin Nippon Biomedical Lab Ltd | Chiral nucleic acid adjuvant |
| KR20240148947A (ko) | 2012-07-13 | 2024-10-11 | 웨이브 라이프 사이언시스 리미티드 | 키랄 제어 |
| SG11201500239VA (en) | 2012-07-13 | 2015-03-30 | Wave Life Sciences Japan | Asymmetric auxiliary group |
| EP2875013B1 (en) * | 2012-07-17 | 2017-11-29 | Glaxosmithkline Intellectual Property (No. 2) Limited | Indolecarbonitriles as selective androgen receptor modulators |
| WO2014118388A1 (en) | 2013-02-04 | 2014-08-07 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
| JP6248948B2 (ja) | 2013-02-08 | 2017-12-20 | 日産化学工業株式会社 | 3環性ピロロピリジン化合物及びjak阻害剤 |
| WO2015108048A1 (ja) | 2014-01-15 | 2015-07-23 | 株式会社新日本科学 | 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤 |
| EP3095460A4 (en) | 2014-01-15 | 2017-08-23 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent |
| WO2015108047A1 (ja) | 2014-01-15 | 2015-07-23 | 株式会社新日本科学 | 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤 |
| ES2917473T3 (es) | 2014-01-16 | 2022-07-08 | Wave Life Sciences Ltd | Diseño quiral |
| EP2924026A1 (en) | 2014-03-28 | 2015-09-30 | Novartis Tiergesundheit AG | Aminosulfonylmethylcyclohexanes as JAK inhibitors |
| AU2015260349B2 (en) | 2014-05-14 | 2019-02-21 | Nissan Chemical Industries, Ltd. | Tricyclic compound and JAK inhibitor |
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| CN115246833A (zh) * | 2021-04-27 | 2022-10-28 | 洛阳惠中兽药有限公司 | 一种奥拉替尼化合物及其中间体化合物的制备方法 |
| CN115246833B (zh) * | 2021-04-27 | 2024-08-13 | 洛阳惠中兽药有限公司 | 一种奥拉替尼化合物及其中间体化合物的制备方法 |
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