IP Library Granted Patent US 12,662,494
Granted Patent B2
US 12,662,494 · App. 17/265,920 · Granted Jun 23, 2026

Optically active bridged piperidine derivative

Inventors: Seiji Kamioka (Toyonaka, JP); Naoaki Shimada (Takatsuki, JP); Hitoshi Ban (Nishinomiya, JP); Kazuto Yamazaki (Ikoma, JP); Akihiko Arakawa (Odawara, JP); Wataru Hirose (Suita, JP)
Assignee: Sumitomo Pharma Co., Ltd.
C07D519/00A61P35/02C07D453/06C07D513/04
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Quick Facts
Patent No.
US 12,662,494
App. No.
17/265,920
Filed
Feb 4, 2021
Granted
Jun 23, 2026
Kind
B2
Art Unit
1693
USPC
546/180
Abstract

The present invention relates to the compound of formula (1a) wherein a-d and p are 1 or 2, R 1 -R 4 are hydrogen atom or the like, and R 18 is —CF 3 or the like, or a pharmaceutically acceptable salt thereof, which has an anticancer effect by inhibiting the binding between a MLL fusion protein that is fused with AF4, AF9, or the like, which is a representative fusion partner gene causing MLL leukemia, and menin.

Claims (15)

1 . A compound selected from the group consisting of

[(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octan-3-yl]{2-[2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)thieno[2,3-b]pyridin-4-yl]-2,7-diazaspiro[3.5]nonan-7-yl}methanone,

4-{7-[(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile,

4-{7-[(1S,3S,4R)-5-methylidene-2-azabicyclo[2.2.1]heptane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile,

[(1S,3S,4R)-5-methylidene-2-azabicyclo[2.2.2]octan-3-yl]{2-[2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)thieno[2,3-b]pyridin-4-yl]-2,7-diazaspiro[3.5]nonan-7-yl}methanone, and

4-{7-[(1S,3S,4R)-5-methylidene-2-azabicyclo[2.2.2]octane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile or pharmaceutically acceptable salt thereof.

2 . The compound of claim 1 where the compound is [(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octan-3-yl]{2-[2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)thieno[2,3-b]pyridin-4-yl]-2,7-diazaspiro[3.5]nonan-7-yl}methanone, or a pharmaceutically acceptable salt thereof.

3 . The compound of claim 1 where the compound is 4-{7-[(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile, or a pharmaceutically acceptable salt thereof.

4 . The compound of claim 1 where the compound is [(1S,3S,4R)-5-methylidene-2-azabicyclo[2.2.2]octan-3-yl]{2-[2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)thieno[2,3-b]pyridin-4-yl]-2,7-diazaspiro[3.5]nonan-7-yl}methanone, or a pharmaceutically acceptable salt thereof.

5 . The compound of claim 1 where the compound is 4-{7-[(1S,3S,4R)-5-methylidene-2-azabicyclo[2.2.2]octane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile, or a pharmaceutically acceptable salt thereof.

6 . A compound selected from the group consisting of [(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octan-3-yl]{2-[2-(2,2,2-trifluoroethyl)-5-(trifluoromethyl)thieno[2,3-b]pyridin-4-yl]-2,7-diazaspiro[3.5]nonan-7-yl}methanone, or a pharmaceutically acceptable salt thereof and 4-{7-[(1S,3S,4R)-5-( 2 H 2 )methylidene-2-azabicyclo[2.2.2]octane-3-carbonyl]-2,7-diazaspiro[3.5]nonan-2-yl}-2-(2,2,2-trifluoroethyl)thieno[2,3-b]pyridine-5-carbonitrile, or a pharmaceutically acceptable salt thereof.

7 . A method for treating a tumor selected from MLL acute leukemia, MLL partial tandem duplicate acute leukemia, NPM mutated acute leukemia, MOZ acute leukemia, NUP98 acute leukemia, CALM acute leukemia, chronic myeloid leukemia, B-cell lymphoma, or multiple myeloma, comprising administering a compound of claim 6 or a pharmaceutically acceptable salt thereof to a patient in need thereof.

8 . The method of claim 7 , wherein the tumor is MLL acute leukemia, or NPM mutated acute leukemia.

9 . A pharmaceutical composition comprising the compound of claim 1 or a pharmaceutically acceptable salt thereof in combination with at least one different agent or a pharmaceutically acceptable salt thereof, wherein the different agent is at least one agent selected from the group consisting of an antitumor alkylating agent, an antitumor antimetabolite, an antitumor antibiotic, a plant-derived antitumor medicament, an antitumor platinum complex compound, an antitumor camptothecin derivative, an antitumor tyrosine kinase inhibitor, an antitumor serine/threonine kinase inhibitor, an antitumor phospholipid kinase inhibitor, an antitumor monoclonal antibody, interferon, an biological response modifier, a hormone preparation, an angiogenic inhibitor, an immune checkpoint inhibitor, an epigenetics-associated molecular inhibitor, a protein post-translational modification inhibitor, a proteasome inhibitor, and other antitumor medicaments.

10 . A method of treating a subject with a tumor comprising administering to a subject with a tumor the compound of claim 1 , and at least one different agent or a pharmaceutically acceptable salt thereof, wherein the different agent is at least one agent selected from an antitumor alkylating agent, an antitumor antimetabolite, an antitumor antibiotic, a plant-derived antitumor medicament, an antitumor platinum complex compound, an antitumor camptothecin derivative, an antitumor tyrosine kinase inhibitor, an antitumor serine/threonine kinase inhibitor, an antitumor phospholipid kinase inhibitor, an antitumor monoclonal antibody, interferon, a biological response modifier, a hormone preparation, an angiogenic inhibitor, an immune checkpoint inhibitor, an epigenetics-associated molecular inhibitor, a protein post-translational modification inhibitor, a proteasome inhibitor, and other antitumor medicaments, wherein the tumor is acute leukemia (including MLL acute leukemia, MLL partial tandem duplicate acute leukemia, NPM mutated acute leukemia, MOZ acute leukemia, NUP98 acute leukemia, and CALM acute leukemia), chronic lymphocytic leukemia, chronic myeloid leukemia, myelodysplastic syndrome, polycythemia vera, malignant lymphoma (including B-cell lymphoma), myeloma (including multiple myeloma), brain tumor, thyroid cancer, small cell lung cancer, non-small cell lung cancer, breast cancer, liver cancer, hepatocellular cancer, colon cancer, rectal cancer, ovarian cancer, bladder cancer, renal cancer, renal cell cancer, prostate cancer, malignant melanoma, Ewing's sarcoma.

Assignments (2)
CHANGE OF NAME Recorded Jun 10, 2022
From: SUMITOMO DAINIPPON PHARMA CO., LTD.
To: SUMITOMO PHARMA CO., LTD.
Reel/Frame 060161/0046 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2021
From: KAMIOKA, SEIJI; SHIMADA, NAOAKI; BAN, HITOSHI; YAMAZAKI, KAZUTO; ARAKAWA, AKIHIKO; HIROSE, WATARU
To: SUMITOMO DAINIPPON PHARMA CO., LTD.
Reel/Frame 055800/0844 →
Priority Claims (1)
JP 2018-149547 · Aug 8, 2018 · national
Continuity (1)
Related Publication 20210198283A1 · Jul 1, 2021
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