NOVEL PYRAZOLE DERIVATIVES Russian patent published in 2019 - IPC C07D471/04 A61K31/437 A61K31/444 A61K31/497 A61K31/506 A61K31/5377 A61P25/16 A61P25/18 A61P25/28 C07D401/04 C07D403/04 C07D417/04 

Abstract RU 2682247 C2

FIELD: chemistry.

SUBSTANCE: invention relates to a compound represented by formula (I) or a pharmaceutically acceptable salt thereof. In formula (I), p is an integer from 0 to 3; q is an integer from 0 to 1; Z is N or CR5; every R1 independently represents a fluorine atom, a chlorine atom, a bromine atom, a cyano group, a methyl group, an ethyl group, an isopropyl group, a tert-butyl group, a vinyl group, a hydroxyethyl group, a cyclopropyl group, a difluoromethyl group, a trifluoromethyl group, a methoxy group, an ethoxyethyl group or an acetyl group, R2 represents a methyl group; every R3 independently represents a fluorine atom or a chlorine atom; R4 represents a phenyl group, a pyridyl group, a pyrolidinyl group or a morpholinyl group, moreover, the phenyl group, pyridyl group, pyrolidinyl group and morpholinyl group, which represent R4, are optionally substituted with one to two groups selected from a fluorine atom, a methyl group, a trifluoromethyl group, a methoxy group, and a methoxymethyl group; R5 represents a hydrogen atom, a fluorine atom; ring A, which is represented by partial structural formula (II), is a 5–6 membered monocyclic heteroaryl group, which has a structure in that the pyrazole ring is directly connected in position 4 to position α in relation to the nitrogen atom of a 5–6-membered monocyclic heteroaryl group, and selected from the group of heteroaryl specified in the claims; R6 represents a methyl group; and condensed ring B that is represented by partial structural formula (III). Also the invention relates to a compound represented by formula (Ib), a compound represented by formula (Id), to individual compounds, to pharmaceutical compositions, to an agent for preventing and / or treating at least one disease or condition associated with PDE10, to a PDE10 inhibitor, to a treatment method, to a compound represented by formula (I ').

EFFECT: technical result: new compounds with inhibitory action against phosphodiesterase 10 (PDE10) are obtained.

34 cl, 59 tbl, 181 ex

Similar patents RU2682247C2

Title Year Author Number
BICYCLIC LACTAMS AND METHODS OF USE THEREOF 2016
  • Patel, Snakhel
  • Gamilton, Gregori
  • Stivala, Krejg
  • Chen, Khuejfen
  • Chzhao, Gujlin
RU2827714C1
BICYCLIC LACTAMS AND METHODS FOR USE THEREOF 2016
  • Patel Snakhel
  • Gamilton Gregori
  • Stivala Krejg
  • Chen Khuejfen
  • Chzhao Gujlin
RU2716136C2
MULTI-SUBSTITUTED AROMATIC COMPOUNDS AS THROMBIN INHIBITORS 2011
  • Short Kevin Majkl
  • Fam Son Minkh
  • Uillyams Devid Charlz
  • Datta Somalee
RU2639876C2
NEW TETRAHYDROPYRIMIDINE CONNECTION OR ITS SALT 2015
  • Minamiguti, Kadzukhisa
  • Okadzima, Sigeo
  • Aoki, Siniti
  • Asai, Masanori
  • Asai, Takakhiro
  • Yamanaka, Khirojosi
  • Dokhi, Suguru
RU2636310C1
CONDENSED HETEROCYCLIC NITROGEN COMPOUNDS AND USING THEM AS INHIBITORS OF AMYLOID BETA PRODUCTION 2010
  • Kitadzava Noritaka
  • Sinmio Dajsuke
  • Ito Koiti
  • Sato Nobuaki
  • Khasegava Daidzu
  • Uemura Tosijuki
  • Vatanabe Toru
RU2515976C2
NOVEL INDOLYSIN COMPOUNDS, METHOD FOR PRODUCING AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEREOF 2014
  • Le-Tiran Arno
  • Le-Digore Terri
  • Stark Zherom-Benua
  • Anlen Zhan-Mishel
  • De-Nantej Gijom
  • Zhanest Olive
  • Dejvidson Dzhejms Eduard Pol
  • Marri Dzhejms Bruk
  • Chen Itszen
RU2693629C2
IDENTIFICATION OF LKB1 MUTATION AS PROGNOSTIC BIOMARKER OF SENSITIVITY TO TOR-KINASE INHIBITORS 2011
  • Sankar Sabita
  • Chopra Radzhesh
  • Sjuj Vehjmin
  • Nin Jujkhun
  • Sju Shujchan'
RU2565034C2
PHENOXYMETHYL DERIVATIVES 2016
  • Khert Zherom
  • Khuntsiker Daniel
  • Kyune Kholger
  • Lyubbers Tomas
  • Martin Rajner E.
  • Mattej Patritsio
  • Najdkhart Verner
  • Rikhter Khans
  • Rudolf Markus
  • Pinar Emmanyuel
RU2746481C1
[1,2,4]TRIAZOLO[1,5-a]PYRIMIDINE-2-YLUREA DERIVATIVE AND ITS APPLICATION 2004
  • Masuda Akira
  • Satokh Esitaka
  • Akijama Judzi
  • Sajga Kan
  • Tojoda Ehriko
RU2348636C2
AKT ACTIVITY INHIBITORS 2006
  • Armstrong Donna Dzh.
  • Khu Ehssa Kh.
  • Kelli Majkl Dzh. Iii
  • Lejton Mark Eh.
  • Li Ivehj
  • Ljan Tszjun'
  • Rodzinak Kevin Dzh.
  • Rossi Majkl A.
  • Sanderson Filip Eh.
  • Van Tszjabin
RU2421454C2

RU 2 682 247 C2

Authors

Okano Akikhiro

Saito Fumikhiko

Makabe Muneesi

Ogava Kouki

Dates

2019-03-18Published

2014-02-26Filed