PL3412672T3 - Postać krystaliczna A 2-butoksy-7-(4-(pirolidyn-1-ylometylo)benzylo)-5H-pirolo[3,2- d]pirymidyno-4-aminy jako agonisty TLR7, sposób wytwarzania i jej zastosowanie - Google Patents

Postać krystaliczna A 2-butoksy-7-(4-(pirolidyn-1-ylometylo)benzylo)-5H-pirolo[3,2- d]pirymidyno-4-aminy jako agonisty TLR7, sposób wytwarzania i jej zastosowanie

Info

Publication number
PL3412672T3
PL3412672T3 PL17747004T PL17747004T PL3412672T3 PL 3412672 T3 PL3412672 T3 PL 3412672T3 PL 17747004 T PL17747004 T PL 17747004T PL 17747004 T PL17747004 T PL 17747004T PL 3412672 T3 PL3412672 T3 PL 3412672T3
Authority
PL
Poland
Prior art keywords
pyrrolo
pyrrolidin
pyrimidin
ylmethyl
butoxy
Prior art date
Application number
PL17747004T
Other languages
English (en)
Inventor
Zhaozhong DING
Fei Sun
Yinghu HU
Yilong ZHOU
Zheng Wang
Rui Zhao
Ling Yang
Original Assignee
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Chia Tai Tianqing Pharmaceutical Group Co., Ltd. filed Critical Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Publication of PL3412672T3 publication Critical patent/PL3412672T3/pl

Links

Classifications

    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
PL17747004T 2016-02-05 2017-02-04 Postać krystaliczna A 2-butoksy-7-(4-(pirolidyn-1-ylometylo)benzylo)-5H-pirolo[3,2- d]pirymidyno-4-aminy jako agonisty TLR7, sposób wytwarzania i jej zastosowanie PL3412672T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN201610082029.8A CN107043379A (zh) 2016-02-05 2016-02-05 一种tlr7激动剂的晶型a、其制备方法和医药用途
EP17747004.4A EP3412672B1 (en) 2016-02-05 2017-02-04 Crystal form a of 2-butoxy-7-(4-(pyrrolidin-1-ylmethyl) benzyl)-5h-pyrrolo[3,2-d]pyrimidin-4-amine as tlr7 agonist, preparation method and use thereof
PCT/CN2017/072891 WO2017133684A1 (zh) 2016-02-05 2017-02-04 一种tlr7激动剂的晶型a、其制备方法和用途

Publications (1)

Publication Number Publication Date
PL3412672T3 true PL3412672T3 (pl) 2021-01-25

Family

ID=59499348

Family Applications (1)

Application Number Title Priority Date Filing Date
PL17747004T PL3412672T3 (pl) 2016-02-05 2017-02-04 Postać krystaliczna A 2-butoksy-7-(4-(pirolidyn-1-ylometylo)benzylo)-5H-pirolo[3,2- d]pirymidyno-4-aminy jako agonisty TLR7, sposób wytwarzania i jej zastosowanie

Country Status (28)

Country Link
US (2) US10442811B2 (pl)
EP (1) EP3412672B1 (pl)
JP (1) JP6889171B2 (pl)
KR (1) KR102393280B1 (pl)
CN (2) CN107043379A (pl)
AR (1) AR107548A1 (pl)
AU (1) AU2017215801B2 (pl)
BR (1) BR112018015880A2 (pl)
CA (1) CA3013518C (pl)
CL (1) CL2018002092A1 (pl)
DK (1) DK3412672T3 (pl)
EA (1) EA035951B1 (pl)
ES (1) ES2830443T3 (pl)
HK (1) HK1259170A1 (pl)
HR (1) HRP20201644T1 (pl)
HU (1) HUE051399T2 (pl)
IL (1) IL260968B (pl)
LT (1) LT3412672T (pl)
MX (1) MX2018009501A (pl)
NZ (1) NZ744884A (pl)
PH (1) PH12018501643A1 (pl)
PL (1) PL3412672T3 (pl)
PT (1) PT3412672T (pl)
SG (1) SG11201806683UA (pl)
SI (1) SI3412672T1 (pl)
TW (1) TWI754629B (pl)
UA (1) UA121161C2 (pl)
WO (1) WO2017133684A1 (pl)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA44334A (fr) 2015-10-29 2018-09-05 Novartis Ag Conjugués d'anticorps comprenant un agoniste du récepteur de type toll
CN107043380A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的马来酸盐、其晶型c、晶型d、晶型e、制备方法和用途
CN107043379A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的晶型a、其制备方法和医药用途
CN107043378A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种吡咯并[3,2-d]嘧啶类化合物的制备方法及其中间体
CN112105620A (zh) * 2018-05-25 2020-12-18 正大天晴药业集团股份有限公司 用于治疗肺癌的tlr7激动剂及其药物组合
JP7287708B2 (ja) 2019-02-08 2023-06-06 プロジェニア インコーポレイテッド Toll-like受容体7または8アゴニストとコレステロールの結合体およびその用途
WO2020188448A1 (en) * 2019-03-15 2020-09-24 Janssen Sciences Ireland Unlimited Company Toll-like receptor agonists for use in the treatment of hepatitis b
US20220184085A1 (en) * 2019-04-23 2022-06-16 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Solid pharmaceutical composition comprising tlr7 agonist
CN115666637A (zh) 2020-03-02 2023-01-31 蛋白科技先锋 基于病原体细胞壁骨架的模拟活病原体的纳米粒子及其制备方法
EP4194006A1 (en) 2020-08-04 2023-06-14 Progeneer Inc. Mrna vaccine comprising adjuvant capable of kinetic control
JP2023536954A (ja) 2020-08-04 2023-08-30 プロジェニア インコーポレイテッド 活性化部位が一時的に不活性化したトール様受容体7または8作用薬と機能性薬物の結合体およびその用途
WO2022031011A1 (ko) 2020-08-04 2022-02-10 성균관대학교산학협력단 동력학적으로 작용하는 아주번트 앙상블

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3376479B2 (ja) * 1991-08-12 2003-02-10 武田薬品工業株式会社 縮合ピリミジン誘導体、その製造法および用途
ES2577514T3 (es) * 2005-08-22 2016-07-15 The Regents Of The University Of California Antagonistas de TLR
KR101687841B1 (ko) 2008-12-09 2016-12-19 길리애드 사이언시즈, 인코포레이티드 톨-유사 수용체의 조절제
US9139590B2 (en) * 2011-02-04 2015-09-22 Duquesne University Of The Holy Spirit Bicyclic and tricyclic pyrimidine tyrosine kinase inhibitors with antitubulin activity and methods of treating a patient
EP2800569B1 (en) 2012-01-05 2018-07-25 Northeastern University Allosteric modulators of cb1 cannabinoid receptors
CN104837840B (zh) 2012-10-10 2017-08-08 爱尔兰詹森科学公司 用于治疗病毒感染及其他疾病的吡咯并[3,2‑d]嘧啶衍生物
WO2014081643A1 (en) * 2012-11-20 2014-05-30 Glaxosmithkline Llc Novel compounds
CN104780924B (zh) * 2012-11-20 2016-09-14 葛兰素史克有限责任公司 干扰素诱导剂化合物
CN104780922B (zh) * 2012-11-20 2016-09-07 葛兰素史克有限责任公司 干扰素诱导剂化合物
CN106232603B (zh) 2014-05-01 2019-07-05 诺华股份有限公司 作为toll-样受体7激动剂的化合物和组合物
CN105367576A (zh) 2014-08-15 2016-03-02 正大天晴药业集团股份有限公司 作为tlr7激动剂的吡咯并嘧啶化合物
US9962388B2 (en) * 2014-08-15 2018-05-08 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Pyrrolopyrimidine compounds used as TLR7 agonist
CN107043380A (zh) 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的马来酸盐、其晶型c、晶型d、晶型e、制备方法和用途
CN107043379A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的晶型a、其制备方法和医药用途

Also Published As

Publication number Publication date
SI3412672T1 (sl) 2021-02-26
CA3013518C (en) 2022-07-19
US10442811B2 (en) 2019-10-15
KR102393280B1 (ko) 2022-05-02
WO2017133684A1 (zh) 2017-08-10
CN108602831A (zh) 2018-09-28
ES2830443T3 (es) 2021-06-03
KR20180104117A (ko) 2018-09-19
TWI754629B (zh) 2022-02-11
US20200039988A1 (en) 2020-02-06
IL260968B (en) 2022-05-01
EA201891768A1 (ru) 2019-01-31
US20190040071A1 (en) 2019-02-07
EP3412672B1 (en) 2020-07-15
MX2018009501A (es) 2018-12-11
US10947245B2 (en) 2021-03-16
HUE051399T2 (hu) 2021-03-01
HRP20201644T1 (hr) 2020-12-25
SG11201806683UA (en) 2018-09-27
EA035951B1 (ru) 2020-09-04
AU2017215801A1 (en) 2018-08-23
AU2017215801B2 (en) 2020-09-10
LT3412672T (lt) 2020-11-10
CN108602831B9 (zh) 2020-12-04
AR107548A1 (es) 2018-05-09
JP2019505533A (ja) 2019-02-28
PH12018501643A1 (en) 2019-06-03
UA121161C2 (uk) 2020-04-10
EP3412672A1 (en) 2018-12-12
TW201728589A (zh) 2017-08-16
EP3412672A4 (en) 2019-07-17
HK1259170A1 (zh) 2019-11-29
DK3412672T3 (da) 2020-10-19
JP6889171B2 (ja) 2021-06-18
CL2018002092A1 (es) 2018-12-07
CN107043379A (zh) 2017-08-15
NZ744884A (en) 2022-09-30
CN108602831B (zh) 2020-11-03
CA3013518A1 (en) 2017-08-10
PT3412672T (pt) 2020-11-11
BR112018015880A2 (pt) 2018-12-26

Similar Documents

Publication Publication Date Title
PL3412672T3 (pl) Postać krystaliczna A 2-butoksy-7-(4-(pirolidyn-1-ylometylo)benzylo)-5H-pirolo[3,2- d]pirymidyno-4-aminy jako agonisty TLR7, sposób wytwarzania i jej zastosowanie
HUE061989T2 (hu) Szubsztituált tieno[2,3-D]pirimidin származékok mint menin-MLL inhibitorai és alkalmazási eljárások
HK1222659A1 (zh) 吡咯並 嘧啶衍生物,它們的製備方法和它們作爲激酶抑制劑的用途
IL247949A0 (en) New histories of pyrazolopyrimidines and their use as malt1 inhibitors
EP3096763A4 (en) Novel process for the preparation of dolutegravir and pharmaceutically acceptable salts thereof
IL253360A0 (en) New crystalline forms of neratinib malate and a process for their preparation
EP3470400A4 (en) CRYSTAL FORM OF OZANIMOD, CRYSTAL FORM OF HYDROCHLORIDE AND MANUFACTURING METHOD THEREFOR
PH12018501641A1 (en) Tlr7 agonist trifluoroacetate salt and crystalline form b thereof, preparation methods and uses
HK1259175A1 (zh) 一種tlr7激動劑的馬來酸鹽、其晶型c、晶型d、晶型e及其製備方法和用途
HK1259183A1 (zh) 一種吡咯並[3,2-d]嘧啶類化合物的製備方法及其中間體
EP3564208A4 (en) PROCESS FOR THE PREPARATION OF A MALONIC ACID DERIVATIVE 2- (CYCLOHEXENYLENE) AND THE USE THEREOF
EP3216791A4 (en) Polymorphic substance of yonkenafil hydrochloride, preparation method therefor, and composition and use thereof
GB2559718B (en) Novel crystalline form of tribenuron-methyl, process for preparation and use thereof
EP3097099A4 (en) An improved process for the preparation of trazodone and hydrochloride salt thereof
EP3175851A4 (en) Use of butenylphthalide, usage method thereof and method for preparing same into pharmaceutical composition
EP3461823A4 (en) PLX3397 HYDROCHLORIDE CRYSTAL FORM, MANUFACTURING METHOD AND USE THEREOF
EP3177625A4 (en) Amorphous form of 4-((4(cyclopentyloxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7h-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-3-methoxy-n-methylbenzamide, compositions thereof and methods of their use
GB201720181D0 (en) Process for preparing novel crystalline form of metsulfuron-methyl and use thereof
UA107549C2 (uk) ПОХІДНІ 4,7-ДИГІДРО-5-АМІНО-3-КАРБОКСАМІДО-6-ЦІАНО[1,2,3]ТРИАЗОЛО[1,5-а]ПІРИМІДИНУ І СПОСІБ ЇХ ОДЕРЖАННЯ
EP3026049A4 (en) Method for preparing benzamide derivative, novel intermediate used in preparation of benzamide, and method for preparing novel intermediate