SG11201804860YA - Crystalline forms of thienopyrimidine compound - Google Patents

Crystalline forms of thienopyrimidine compound

Info

Publication number
SG11201804860YA
SG11201804860YA SG11201804860YA SG11201804860YA SG11201804860YA SG 11201804860Y A SG11201804860Y A SG 11201804860YA SG 11201804860Y A SG11201804860Y A SG 11201804860YA SG 11201804860Y A SG11201804860Y A SG 11201804860YA SG 11201804860Y A SG11201804860Y A SG 11201804860YA
Authority
SG
Singapore
Prior art keywords
hwaseong
gyeonggi
international
dongtangiheung
crystalline forms
Prior art date
Application number
SG11201804860YA
Inventor
Jae Hyuk Jung
Jong Ouk Baek
Sun Young Jung
Eun Joo Kwak
Hee Cheol Kim
Tae Hee Ha
Original Assignee
Hanmi Pharmaceutical 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 Hanmi Pharmaceutical Co Ltd filed Critical Hanmi Pharmaceutical Co Ltd
Publication of SG11201804860YA publication Critical patent/SG11201804860YA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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

Abstract

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property -, Organization 111111110111101110101011111010111110111011101111011011111111001111101111011111 International Bureau ... .1 j ..... .....1 (10) International Publication Number (43) International Publication Date WO 2017/116193 Al 6 July 2017 (06.07.2017) WI P0 I P CT (51) International Patent Classification: (74) Agent: Y.P.LEE, MOCK & PARTNERS; 12F Daelim C07D 495/04 (2006.01) Acrotel, 13 Eonju-ro 30-gil, Gangnam-gu, Seoul 06292 (KR). (21) International Application Number: PCT/KR2016/015536 (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, (22) International Filing Date: AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, 30 December 2016 (30.12.2016) BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, (25) Filing Language: English DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, (26) Publication Language: English KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, (30) Priority Data: MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, 10-2015-0190854 NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, 31 December 2015 (31.12.2015) KR RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, (71) Applicant: HANMI PHARM. CO ., LTD. [KR/KR]; 214, ZA, ZM, ZW. Muha-ro, Paltan-myeon, Hwaseong-si, Gyeonggi-do 18536 (KR). (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (72) Inventors: JUNG, Jae Hyuk; 550, Dongtangiheung-ro, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, Hwaseong-si, Gyeonggi-do 18469 (KR). BAEK, Jong TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, Ouk; 550, Dongtangiheung-ro, Hwaseong-si, Gyeonggi-do TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, 18469 (KR). JUNG, Sun Young; 550, Dongtangi- DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, heung-ro, Hwaseong-si, Gyeonggi-do 18469 (KR). LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, KWAK, Eun Joo; 550, Dongtangiheung-ro, Hwaseong-si, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, Gyeonggi-do 18469 (KR). KIM, Hee Cheol; 550, GW, KM, ML, MR, NE, SN, TD, TG). Dongtangiheung-ro, Hwaseong-si, Gyeonggi-do 18469 (KR). HA, Tae Hee; 550, Dongtangiheung-ro, Hwaseong- Published: si, Gyeonggi-do 18469 (KR). — with international search report (Art. 21(3)) (54) Title: CRYSTALLINE FORMS OF THIENOPYRIMIDINE COMPOUND - 2000 175 - 2 :' g 1000-: _ en _ C:7 Il 1-1 1-1 IN 1-1 (57) : The present invention 0 d]pyrimidin-4-yloxy)phenyl)acrylamide, \" used for the preparation of a pharmaceutical 111111111111 11111111111 1 111 I 111 I 1 10 20 30 40 2Theta (Degree) relates to crystalline forms of N-(3-(2-(4-(4-methylpiperazin-1-yl)phenylamino)thieno[3,2- and pharmaceutical compositions containing the same. The crystalline composition containing the same as an active ingredient. forms can be easily
SG11201804860YA 2015-12-31 2016-12-30 Crystalline forms of thienopyrimidine compound SG11201804860YA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR20150190854 2015-12-31
PCT/KR2016/015536 WO2017116193A1 (en) 2015-12-31 2016-12-30 Crystalline forms of thienopyrimidine compound

Publications (1)

Publication Number Publication Date
SG11201804860YA true SG11201804860YA (en) 2018-07-30

Family

ID=59225209

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201804860YA SG11201804860YA (en) 2015-12-31 2016-12-30 Crystalline forms of thienopyrimidine compound

Country Status (16)

Country Link
US (1) US10464946B2 (en)
EP (1) EP3380482A4 (en)
JP (1) JP2019504046A (en)
KR (1) KR20180089904A (en)
CN (1) CN108473507A (en)
AU (1) AU2016382385A1 (en)
BR (1) BR112018013364A2 (en)
CA (1) CA3010315A1 (en)
HK (1) HK1252842A1 (en)
IL (1) IL259982A (en)
MX (1) MX2018008005A (en)
PH (1) PH12018501331A1 (en)
RU (1) RU2018122825A (en)
SG (1) SG11201804860YA (en)
TW (1) TW201726686A (en)
WO (1) WO2017116193A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20170050453A (en) * 2015-10-30 2017-05-11 한미약품 주식회사 Novel process for preparing thienopyrimidine compound and intermediates used therein
AU2016382384A1 (en) * 2015-12-31 2018-07-12 Hanmi Pharm. Co., Ltd. Crystalline forms of hydrochloride salts of thienopyrimidine compound
KR20200114776A (en) * 2019-03-29 2020-10-07 한미약품 주식회사 Crystalline forms of acid addition salts of furopyrimidine compound

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112012033253A2 (en) * 2010-06-23 2016-11-22 Hanmi Science Co Ltd novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity
WO2015112705A2 (en) * 2014-01-24 2015-07-30 Clovis Oncology, Inc. Therapeutic combinations for treating cancer
TW201622744A (en) * 2014-03-04 2016-07-01 美國禮來大藥廠 Combination therapy for cancer
WO2016025641A1 (en) * 2014-08-13 2016-02-18 Celgene Avilomics Research, Inc. Combinations of an erk inhibitor and an egfr inhibitor and related methods
CN107108649B (en) * 2014-12-30 2019-08-09 韩美药品株式会社 Be used to prepare Thienopyrimidine compound novel method and its used in intermediate
KR20170050453A (en) * 2015-10-30 2017-05-11 한미약품 주식회사 Novel process for preparing thienopyrimidine compound and intermediates used therein

Also Published As

Publication number Publication date
TW201726686A (en) 2017-08-01
CN108473507A (en) 2018-08-31
KR20180089904A (en) 2018-08-09
RU2018122825A3 (en) 2020-02-28
BR112018013364A2 (en) 2018-12-04
IL259982A (en) 2018-07-31
HK1252842A1 (en) 2019-06-06
MX2018008005A (en) 2019-03-14
AU2016382385A1 (en) 2018-07-12
US20190016733A1 (en) 2019-01-17
PH12018501331A1 (en) 2019-02-18
EP3380482A4 (en) 2019-05-15
JP2019504046A (en) 2019-02-14
RU2018122825A (en) 2020-02-04
US10464946B2 (en) 2019-11-05
EP3380482A1 (en) 2018-10-03
WO2017116193A1 (en) 2017-07-06
CA3010315A1 (en) 2017-07-06

Similar Documents

Publication Publication Date Title
SG11201804132UA (en) Eif4-a-inhibiting compounds and methods related thereto
SG11201804170RA (en) Polycyclic tlr7/8 antagonists and use thereof in the treatment of immune disorders
SG11201909278SA (en) Fungicidal oxadiazoles
SG11201804152RA (en) Heterocyclic compounds as immunomodulators
SG11201808878UA (en) Heterocyclic compounds as ret kinase inhibitors
SG11201810171SA (en) Kras g12c inhibitors
SG11201803686UA (en) Prodrugs of a jak inhibitor compound for treatment of gastrointestinal inflammatory disease
SG11201805300QA (en) Heterocyclic compounds as immunomodulators
SG11201807301SA (en) Spiro-condensed pyrrolidine derivatives as deubiquitylating enzymes (dub) inhibitors
SG11201805380YA (en) Urea-based prostate specific membrane antigen (psma) inhibitors for imaging and therapy
SG11201408094YA (en) Neprilysin inhibitors
SG11201907544VA (en) Jak inhibitors containing a 4-membered heterocyclic amide
SG11201907356SA (en) Piperidine-substituted mnk inhibitors and methods related thereto
SG11201408095XA (en) Fibroblast growth factor 21 proteins
SG11201804811WA (en) Fenfluramine compositions and methods of preparing the same
SG11201909376TA (en) Crystalline forms of a jak inhibitor compound
SG11201408641UA (en) Phenoxyethyl piperidine compounds
SG11201808566WA (en) Polymorphic form of n-{6-(2-hydroxypropan-2-yl)-2-[2-(methylsulphonyl)ethyl]-2h-indazol-5-yl}-6-(trifluoromethyl)pyridine-2-carboxamide
SG11201805368YA (en) Anthelmintic depsipeptide compounds
SG11201906436VA (en) Novel heterocyclic compound, its preparation method, and pharmaceutical composition comprising the same
SG11201909615YA (en) Salt of an aminopyridine derivative compound, a crystalline form thereof, and a process for preparing the same
SG11201407546QA (en) Novel ring-substituted n-pyridinyl amides as kinase inhibitors
SG11201809830WA (en) Selective reduction of cysteine-engineered antibodies
SG11201407184PA (en) Process for preparation of optically pure and optionally substituted 2- (1 -hydroxy- alkyl) - chromen - 4 - one derivatives and their use in preparing pharmaceuticals
SG11201909807TA (en) Methods of manufacturing of niraparib