CN112888687A - 三氟甲基取代的磺酰胺类选择性bcl-2抑制剂 - Google Patents

三氟甲基取代的磺酰胺类选择性bcl-2抑制剂 Download PDF

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CN112888687A
CN112888687A CN201980067260.1A CN201980067260A CN112888687A CN 112888687 A CN112888687 A CN 112888687A CN 201980067260 A CN201980067260 A CN 201980067260A CN 112888687 A CN112888687 A CN 112888687A
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compound
preparation
methyl
membered heterocycloalkyl
dmso
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CN112888687B (zh
Inventor
刘飞
丰巍伟
王斌
徐宏江
汪纪楠
张喜全
王善春
刘彦龙
张健青
姚绎炎
唐旭静
施伟
张洪英
李洋
汤松
朱益忠
刘利民
顾红梅
杨玲
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Chia Tai Tianqing Pharmaceutical Group Co Ltd
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Chia Tai Tianqing Pharmaceutical Group Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

公开了包括三氟甲基取代的磺酰胺类选择性BCL‑2抑制剂,具体而言公开式I化合物、其立体异构体或其药学上可接受的盐、其制备方法以及该化合物的药物组合物,还公开了该化合物以及包含该化合物的药物组合物在治疗与抗凋亡蛋白BCL‑2相关疾病例如癌症中的用途。

Description

PCT国内申请,说明书已公开。

Claims (15)

  1. PCT国内申请,权利要求书已公开。
CN201980067260.1A 2018-10-29 2019-10-29 三氟甲基取代的磺酰胺类选择性bcl-2抑制剂 Active CN112888687B (zh)

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CN202310104396.3A CN116199686A (zh) 2018-10-29 2019-10-29 三氟甲基取代的磺酰胺类化合物

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CN2018112685722 2018-10-29
CN201811268572 2018-10-29
CN201910249783X 2019-03-29
CN201910249783 2019-03-29
CN2019109335130 2019-09-29
CN201910933513 2019-09-29
PCT/CN2019/113963 WO2020088442A1 (zh) 2018-10-29 2019-10-29 三氟甲基取代的磺酰胺类选择性bcl-2抑制剂

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US (1) US20220002290A1 (zh)
EP (1) EP3858832A4 (zh)
JP (1) JP7473545B2 (zh)
KR (1) KR20210086680A (zh)
CN (2) CN116199686A (zh)
AU (1) AU2019372640B2 (zh)
BR (1) BR112021008323A2 (zh)
CA (1) CA3117849A1 (zh)
IL (1) IL282632B2 (zh)
MX (1) MX2021004856A (zh)
PH (1) PH12021550958A1 (zh)
SG (1) SG11202104322YA (zh)
WO (1) WO2020088442A1 (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115260191A (zh) * 2022-09-29 2022-11-01 上海睿跃生物科技有限公司 哌啶类化合物及其制备方法和应用

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022533740A (ja) * 2019-05-24 2022-07-25 チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド メチル基及びトリフルオロメチル基を含む二置換スルファミド系選択的bcl-2阻害剤
TW202144350A (zh) * 2020-04-29 2021-12-01 大陸商正大天晴藥業集團股份有限公司 三氟甲基和氯雙取代的磺醯胺類選擇性bcl-2抑制劑的晶體
WO2022161496A1 (en) * 2021-02-01 2022-08-04 Ascentage Pharma (Suzhou) Co., Ltd. Sulfonyl benzamide derivatives as bcl-2 inhibitors
WO2022253313A1 (zh) 2021-06-04 2022-12-08 正大天晴药业集团股份有限公司 三氟甲基取代的磺酰胺类化合物的磷酸酯
WO2024012449A1 (zh) * 2022-07-12 2024-01-18 正大天晴药业集团股份有限公司 含有三氟甲基基团的化合物
WO2024032776A1 (en) * 2022-08-12 2024-02-15 Fochon Biosciences, Ltd. Compounds as bcl-2 inhibitors

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010065824A2 (en) * 2008-12-04 2010-06-10 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
CN102307872A (zh) * 2008-12-05 2012-01-04 雅培制药有限公司 作为用于治疗癌症和免疫疾病的bcl-2-选择性诱发细胞凋亡药剂的磺酰胺衍生物
CN104876927A (zh) * 2009-05-26 2015-09-02 艾伯维巴哈马有限公司 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103402521B (zh) 2010-11-23 2016-01-20 艾伯维巴哈马有限公司 使用选择性的bcl-2抑制剂的治疗方法
US20140275082A1 (en) 2013-03-14 2014-09-18 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
WO2018041248A1 (zh) 2016-09-01 2018-03-08 北京赛林泰医药技术有限公司 Bcl-2选择性抑制剂及其制备和用途

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010065824A2 (en) * 2008-12-04 2010-06-10 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
CN102307872A (zh) * 2008-12-05 2012-01-04 雅培制药有限公司 作为用于治疗癌症和免疫疾病的bcl-2-选择性诱发细胞凋亡药剂的磺酰胺衍生物
CN104876927A (zh) * 2009-05-26 2015-09-02 艾伯维巴哈马有限公司 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115260191A (zh) * 2022-09-29 2022-11-01 上海睿跃生物科技有限公司 哌啶类化合物及其制备方法和应用

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Publication number Publication date
CN116199686A (zh) 2023-06-02
CN112888687B (zh) 2023-01-24
AU2019372640A1 (en) 2021-06-03
IL282632A (en) 2021-06-30
CA3117849A1 (en) 2020-05-07
EP3858832A1 (en) 2021-08-04
BR112021008323A2 (pt) 2021-08-03
WO2020088442A1 (zh) 2020-05-07
JP7473545B2 (ja) 2024-04-23
SG11202104322YA (en) 2021-05-28
MX2021004856A (es) 2021-10-13
JP2022506442A (ja) 2022-01-17
AU2019372640B2 (en) 2022-08-04
US20220002290A1 (en) 2022-01-06
IL282632B1 (en) 2024-02-01
PH12021550958A1 (en) 2021-11-29
KR20210086680A (ko) 2021-07-08
IL282632B2 (en) 2024-06-01
EP3858832A4 (en) 2022-06-08

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