IP Library › Granted Patent US 12,629,358
Granted Patent B2
US 12,629,358 · App. 17/613,311 · Granted May 19, 2026

Compound used as RET kinase inhibitor and application thereof

Inventors: Jun Li (Huzhou, CN); Maolin Zheng (Huzhou, CN); Chengshan Niu (Huzhou, CN); Apeng Liang (Huzhou, CN); Yusheng Wu (Huzhou, CN)
Assignee: TYK MEDICINES, INC.
A61K31/444A61K31/4355A61K31/437A61K31/4725A61K31/497A61K31/4985A61K31/506A61K31/519
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Quick Facts
Patent No.
US 12,629,358
App. No.
17/613,311
Granted
May 19, 2026
Kind
B2
Abstract

The present invention belongs to the field of medical technology and specifically disclosed is a compound represented by formula (I′), or a pharmaceutically acceptable salt, stereoisomer, solvate or prodrug thereof, and each symbol therein is as defined in the claims. The compound of the present invention may be used as a drug for regulating RET kinase activity or treating RET-related diseases, and has better pharmacokinetic properties.

Claims (18)

1 . A compound, or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof has a structure represented by Formula 6′,

wherein X 2 , X 9 , and X 10 are each independently selected from N or CR 5 ;

X 7 and X 8 are each independently selected from N or C; and

R 5 is each independently selected from hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C1-C6 alkoxy, C1-C6 alkylamino, halogen, C1-C6 heteroalkyl, cycloalkyl, nitro, cyano, or amino; wherein alkyl, alkenyl, alkynyl, alkoxy, alkylamino, heteroalkyl, and cycloalkyl are each independently substituted by 0-5 R a ; R a is selected from C1-C6 alkyl, halogen, hydroxy, C1-C6 heteroalkyl, C1-C6 alkoxy, C1-C6 alkylamino, cycloalkyl, heterocycloalkyl, or cyano;

ring Q2 is selected from five-membered, six-membered or seven-membered saturated ring, unsaturated ring, aromatic ring, or heteroaromatic ring, and can contain 0-3 heteroatoms selected from N, O, or S, and any hydrogen atom on the ring Q2 can be substituted by deuterium, hydroxy, halogen, cyano, ester, amide, ketocarbonyl, amino, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 thioalkyl, C1-C6 alkoxy, C1-C6 heteroalkyl, C1-C6 alkylamino, C3-C6 cycloalkyl, C3-C8 cycloalkylamino, aryl, or heteroaryl.

2 . A compound, or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof, wherein the compound is selected from the following compounds:

3 . The compound of claim 1 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof, wherein the pharmaceutically acceptable salt is an inorganic acid salt or an organic acid salt, wherein the inorganic acid salt is selected from hydrochloride, hydrobromide, hydroiodide, sulfate, bisulfate, nitrate, phosphate, or acid phosphate; the organic acid salt is selected from formate, acetate, trifluoroacetate, propionate, pyruvate, hydroxyacetate, oxalate, malonate, fumarate, maleate, lactate, malate, citrate, tartrate, methanesulfonate, ethanesulfonate, benzenesulfonate, salicylate, picrate, glutamate, ascorbate, camphorate, or camphor sulfonate.

4 . A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof, and a pharmaceutically acceptable carrier.

5 . A method of modulating RET kinase activity or treating RET-related diseases comprising administering to a subject in need thereof an effective amount of the compound of claim 1 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof.

6 . The method of claim 5 , wherein the RET-related diseases comprise a cancer.

7 . The compound of claim 1 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof, wherein

is selected from

R 5 is independently selected from H, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylamino, nitro, cyano, or amino;

Y 2 and Y 3 are each independently selected from O, N, and CR 13 ;

R 13 is each independently selected from H, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylamino, cyano, or amino.

8 . A pharmaceutical composition, wherein the pharmaceutical composition comprises a therapeutically effective amount of the compound of claim 2 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof, and a pharmaceutically acceptable carrier.

9 . A method of modulating RET kinase activity or treating RET-related diseases comprising administering to a subject in need thereof an effective amount of the compound of claim 2 , or the pharmaceutically acceptable salt, stereoisomer, or solvate thereof.

10 . The method of claim 9 , wherein the RET-related diseases comprise a cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2021
From: LI, JUN; ZHENG, MAOLIN; NIU, CHENGSHAN; LIANG, APENG; WU, YUSHENG
To: TYK MEDICINES, INC.
Reel/Frame 058183/0079 →
Priority Claims (1)
CN 201910417078.6 · May 20, 2019 · national
Continuity (1)
Related Publication 20220233513A1 · Jul 28, 2022
References Cited (34)
US 20060084650A1 · Dong · 2006 [cited by examiner]
US 20140179668A1 · Chakravarty et al. · 2014 [cited by applicant]
US 20160083369A1 · Shia et al. · 2016 [cited by applicant]
US 20170121312A1 · Brubaker et al. · 2017 [cited by applicant]
CN 101184758A · 2008 [cited by applicant]
CN 101535303A · 2009 [cited by applicant]
CN 104039956A · 2014 [cited by applicant]
CN 108473468A · 2018 [cited by applicant]
CN 108689994A · 2018 [cited by applicant]
CN 109180677A · 2019 [cited by applicant]
CN 111285882A · 2020 [cited by applicant]
CN 111961034A · 2020 [cited by applicant]
EP 0995750A1 · 2000 [cited by applicant]
WO 200068208A1 · 2000 [cited by applicant]
WO 2006104889A2 · 2006 [cited by applicant]
WO 2007147103A2 · 2007 [cited by applicant]
WO 2007147109A2 · 2007 [cited by applicant]
WO 2009050236A1 · 2009 [cited by applicant]
WO 2014105958A2 · 2014 [cited by applicant]
WO 2016083369A1 · 2016 [cited by applicant]
WO 2018017983A1 · 2018 [cited by applicant]
WO 2018022761A1 · 2018 [cited by applicant]
WO 2018136663A1 · 2018 [cited by applicant]
WO WO2018213329A1 · 2018 [cited by examiner]
WO WO2020175968A1 · 2020 [cited by examiner]
Fleming et al., J. Med. Chem., 2010, 53, 7902-7917 (Year: 2010). [cited by examiner]
Acharya et al., Expert Opinion on Therapeutic Patents, 2022, 32, 1067-1077 (Year: 2022). [cited by examiner]
Han, H., AAPS Pharmsci., 2000, 2, 1-11 (Year: 2000). [cited by examiner]
International Search Report and Written Opinion; PCT Application No. PCT/CN2020/091425; mailed Jun. 30, 2020. [cited by applicant]
English abstract of International Search Report; retrieved from https://patentscope.wipo.int/search/en/detail.jsf?docld=WO2020233641&_cid=P10-KW15WP-52452-1; on Nov. 15, 2021. [cited by applicant]
English abstract of CN108473468; retrieved from www.espacenet.com on Nov. 15, 2021. [cited by applicant]
English abstract of CN109180677; retrieved from www.espacenet.com on Nov. 15, 2021. [cited by applicant]
English abstract of CN108689994; retrieved from www.espacenet.com on Nov. 15, 2021. [cited by applicant]
Database Registry [Online], “1-[6, 7-dihydro-2-(4-morpholinylmethyl)-SH cyclopenta[4,5]thieno[2, 3-d]pyri midin-4-yl]-N-(phenylmethyl)-4-Piperidinecarboxamide” (Abstract) Database Accession No. 877136-72-6, Chemical Abs… [cited by applicant]