MX2023004668A - Forma cristalina de acido 2-{4-[n-(5,6-difenilpirazin-2-il)-n-isop ropilamino]butiloxi}acetico. - Google Patents

Forma cristalina de acido 2-{4-[n-(5,6-difenilpirazin-2-il)-n-isop ropilamino]butiloxi}acetico.

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Publication number
MX2023004668A
MX2023004668A MX2023004668A MX2023004668A MX2023004668A MX 2023004668 A MX2023004668 A MX 2023004668A MX 2023004668 A MX2023004668 A MX 2023004668A MX 2023004668 A MX2023004668 A MX 2023004668A MX 2023004668 A MX2023004668 A MX 2023004668A
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Mexico
Prior art keywords
crystal
compound
diffraction
cukî
radiation
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MX2023004668A
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English (en)
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Toshio Fujiwara
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Nippon Shinyaku Co Ltd
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Publication of MX2023004668A publication Critical patent/MX2023004668A/es

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/20Nitrogen atoms
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    • 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
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D241/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
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  • Steroid Compounds (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)

Abstract

Un objeto principal de la presente invención consiste en proporcionar un nuevo cristal de ácido 2-{4-[N-(5,6-difenilpirazin -2-il)-N-isopropilamino]butiloxi}acético (de ahora en más en la presente, mencionado como "compuesto B"). Un cristal de la forma I de compuesto B, que muestra picos en ángulos de difracción (2?) de 6,4?, 8,1?, 9,5?, 10,9?, 13,2?, 15,7?, 17,0?, 19,5?, 20,3?, 21,0? y 22,8? en un espectro de difracción de polvos por rayos X obtenido usando una radiación Cu-Ka (?=1,54 Å). Un cristal de la forma II de compuesto B, que muestra picos en ángulos de difracción (2?) de 9,6?, 11,4?, 11,7?, 16,3?, 17,5?, 18,5?, 18,7?, 19,9?, 20,1?, 21,0? y 24,6? en un espectro de difracción de polvos por rayos X obtenido usando una radiación Cu-Ka (?=1,54 Å).
MX2023004668A 2017-09-28 2020-07-13 Forma cristalina de acido 2-{4-[n-(5,6-difenilpirazin-2-il)-n-isop ropilamino]butiloxi}acetico. MX2023004668A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2017187296 2017-09-28

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MX2023004668A true MX2023004668A (es) 2023-05-19

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MX2020007315A MX2020007315A (es) 2017-09-28 2018-09-27 Cristal.
MX2023004668A MX2023004668A (es) 2017-09-28 2020-07-13 Forma cristalina de acido 2-{4-[n-(5,6-difenilpirazin-2-il)-n-isop ropilamino]butiloxi}acetico.

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EP (2) EP3689854A4 (es)
JP (3) JP7160043B2 (es)
KR (2) KR102675320B1 (es)
CN (2) CN111263754A (es)
AR (1) AR112842A1 (es)
AU (2) AU2018338856B2 (es)
BR (1) BR112020005428A2 (es)
CA (1) CA3076877A1 (es)
CO (1) CO2020003424A2 (es)
IL (1) IL273430A (es)
MX (2) MX2020007315A (es)
PH (1) PH12020550149A1 (es)
RU (1) RU2020112117A (es)
SG (1) SG11202002443QA (es)
TW (2) TWI801421B (es)
UA (1) UA126928C2 (es)
WO (1) WO2019065792A1 (es)

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TWI801421B (zh) * 2017-09-28 2023-05-11 日商日本新藥股份有限公司 結晶
WO2021023271A1 (zh) * 2019-08-06 2021-02-11 南京明德新药研发有限公司 作为前列环素受体激动剂的化合物的晶型及其制备方法
TW202114998A (zh) * 2019-08-19 2021-04-16 日商日本新藥股份有限公司

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Publication number Priority date Publication date Assignee Title
TWI316055B (es) 2001-04-26 2009-10-21 Nippon Shinyaku Co Ltd
DK2246336T3 (da) 2008-02-28 2020-07-20 Nippon Shinyaku Co Ltd Fibroseinhibitor
WO2009154246A1 (ja) 2008-06-19 2009-12-23 日本新薬株式会社 勃起不全治療剤
WO2009157397A1 (ja) 2008-06-23 2009-12-30 日本新薬株式会社 非ステロイド性抗炎症剤投与に伴う腸管傷害治療剤
CN102065864B (zh) 2008-06-23 2012-11-21 日本新药株式会社 炎性肠病治疗剂
WO2009157396A1 (ja) 2008-06-23 2009-12-30 日本新薬株式会社 脊柱管狭窄症治療剤
MY163762A (en) 2008-07-23 2017-10-31 Toray Industries Therapeutic agent for chronic renal failure
KR102705198B1 (ko) * 2009-06-26 2024-09-11 니뽄 신야쿠 가부시키가이샤 결정
CN106279047B (zh) * 2015-05-13 2019-05-03 普济生物科技(台州)有限公司 一种前列环素受体激动剂的制备方法
WO2017042828A2 (en) * 2015-09-10 2017-03-16 Megafine Pharma (P) Ltd. Process for the preparation of selexipag and intermediates thereof
WO2017060827A1 (en) 2015-10-07 2017-04-13 Lupin Limited An imrpoved process for the preparation of selexipag or its pharmaceutically acceptable salts
EP3481807A4 (en) * 2016-07-05 2020-01-15 Maithri Drugs Private Limited NEW PROCESS FOR THE PREPARATION OF 2- {4 - [(5,6-DIPHENYL PYRAZIN-2-YL) (ISOPROPYL) AMINO] BUTOXY} -N- (METHYLSULFONYL) ACETAMIDE AND NEW POLYMORPHS THEREOF
CN106957269A (zh) * 2016-12-21 2017-07-18 南京艾德凯腾生物医药有限责任公司 一种成人肺动脉高压治疗药物赛乐西帕的制备方法
CN107365275B (zh) * 2017-06-14 2020-07-03 杭州华东医药集团新药研究院有限公司 高纯度的赛乐西帕
TWI801421B (zh) * 2017-09-28 2023-05-11 日商日本新藥股份有限公司 結晶

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US10906879B2 (en) 2021-02-02
TWI834536B (zh) 2024-03-01
EP3689854A4 (en) 2021-06-09
IL273430A (en) 2020-05-31
EP3689854A1 (en) 2020-08-05
PH12020550149A1 (en) 2021-02-08
EP4371617A3 (en) 2024-08-07
BR112020005428A2 (pt) 2020-09-29
UA126928C2 (uk) 2023-02-22
KR102675320B1 (ko) 2024-06-14
TW202332673A (zh) 2023-08-16
AU2018338856B2 (en) 2023-09-21
JP2024045685A (ja) 2024-04-02
US20210114995A1 (en) 2021-04-22
JPWO2019065792A1 (ja) 2020-10-22
JP7160043B2 (ja) 2022-10-25
CO2020003424A2 (es) 2020-06-19
AR112842A1 (es) 2019-12-18
CA3076877A1 (en) 2019-04-04
CN111263754A (zh) 2020-06-09
US20200223804A1 (en) 2020-07-16
US11655218B2 (en) 2023-05-23
JP7485738B2 (ja) 2024-05-16
TW201920121A (zh) 2019-06-01
CN117510418A (zh) 2024-02-06
MX2020007315A (es) 2020-08-20
SG11202002443QA (en) 2020-04-29
JP2022173401A (ja) 2022-11-18
AU2018338856A1 (en) 2020-04-16
KR20200060393A (ko) 2020-05-29
KR20240042215A (ko) 2024-04-01
EP4371617A2 (en) 2024-05-22
US20230303500A1 (en) 2023-09-28
AU2023274142A1 (en) 2023-12-21
TWI801421B (zh) 2023-05-11
RU2020112117A (ru) 2021-10-28
WO2019065792A1 (ja) 2019-04-04

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