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Fused bicyclic pyrimidine derivatives and uses thereof

a technology of pyrimidine and derivatives, applied in the field of pyrimidine derivatives of fused bicyclic compounds, can solve the problems of limited drugs that can exploit the loss of pyrimidine, and achieve the effect of reducing, slowing, stopping or preventing the activity of a particular biological process

Active Publication Date: 2018-12-27
DANA FARBER CANCER INST INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The text describes a group of compounds that are designed to become active in the body. These compounds have cleavable groups that can be converted into different forms under certain conditions. One example is a compound called a prodrug, which can be converted to another compound that is more effective in treating a condition. The patented compounds are useful in treating or preventing certain conditions. The technical effect of this patent is to provide a way to create compounds that can be transformed into active forms in the body, which can improve the effectiveness of treating or preventing diseases.

Problems solved by technology

Unfortunately the duration of response to targeted kinase inhibitors is typically less than 2 years, and most lung tumors do not express an oncogene that is targeted by an available drug.
For example, loss of p53 is a common event in lung cancer, but there are currently limited drugs that can exploit its loss.

Method used

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  • Fused bicyclic pyrimidine derivatives and uses thereof
  • Fused bicyclic pyrimidine derivatives and uses thereof
  • Fused bicyclic pyrimidine derivatives and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

example 2

of Compound MFH-2-25-1

[0363]

5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (MFH-2-6-1)

[0364]A mixture of 5-nitro-1H-pyrrolo[2,3-b]pyridine (300 mg, 1.84 mmol) and benzenesulfonyl chloride (812 mg, 4.6 mmol) in pyridine (3 mL) was refluxed for 6 hours. Then the reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel (PE / EA=0-50%) to obtain MFH-2-6-1 (530 mg, yield 95%). LCMS (m / z): 304 [M+H]+.

1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-amine (MFH-2-7-1)

[0365]A mixture of MFH-2-6-1 (530 mg, 1.75 mmol) and 10% Pd / C (50 mg) in MeOH (20 mL) was stirred overnight at room temperature with an H2 balloon. The mixture was filtered through CELITE, and solvent was removed to give MFH-2-7-1 (230 mg, yield 48%). LCMS (m / z): 274 [M+H]+.

2-chloro-N-(1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)thieno[3,2-d]pyrimidin-4-amine (MFH-2-8-1)

[0366]A solution of MFH-2-7-1 (230 mg, 0.84 mmol), 2,4-dichlorothieno[3,2-d]pyrimidine (173 mg, 0.84 mmol) and...

example 3

of Compound MFH-2-40-1

[0373]

4-(1-(2-chlorothieno[3,2-d]pyrimidin-4-yl)piperidin-4-yl)morpholine (MFH-2-29-1)

[0374]To a solution of 2,4-dichlorothieno[3,2-d]pyrimidine (300 mg, 1.46 mmol) and DIPEA (227 mg, 1.76 mmol) in DCM (5 mL) was added 4-(piperidin-4-yl)morpholine (274 mg, 1.61 mmol) in DCM (3 mL) dropwise at room temperature. The mixture was stirred at room temperature for 3 hours and then was concentrated under reduced pressure. The residue was purified by silica gel (NH3 / MeOH(1.75N) / DCM=0-20%) to obtain MFH-2-29-1 (496 mg, yield 100%). LCMS (m / z): 339 [M+H]+.

tert-butyl3-(4-(4-morpholinopiperidin-1-yl)thieno[3,2-d]pyrimidin-2-ylamino)phenylcarbamate (MFH-2-32-1)

[0375]A solution of MFH-2-29-1 (496 mg, 1.46 mmol), tert-butyl 3-aminophenylcarbamate (335 mg, 1.61 mmol), 2-Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (105 mg, 0.22 mmol), K2CO3 (243 mg, 1.76 mmol), and Pd2(dba)3 (201 mg, 0.22 mmol) in tert-Butanol (10 mL) was refluxed for 5 hours under N2 atmosphere. The mix...

example 4

of Compound MFH-2-44-1

[0380]

5-methoxy-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (MFH-2-10-1)

[0381]A mixture of 5-methoxy-1H-pyrrolo[2,3-b]pyridine (800 mg, 5.4 mmol) and benzenesulfonyl chloride (1.9 g, 10.8 mmol) in pyridine (8 mL) was refluxed overnight. Then the reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel (PE / EA=0-50%) to obtain MFH-2-10-1 (646 mg, yield 42%). LCMS (m / z): 289 [M+H]+.

1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-ol (MFH-2-13-1)

[0382]To a solution of MFH-2-10-1 (646 mg, 2.25 mmol) in DCM (20 mL) was added boron trichloride in hexane (1 mol / L, 22.5 ml, 22.5 mmol) dropwise at −15° C. The mixture was warmed to room temperature and the mixture was stirred overnight. After completion, water (50 ml) was added at 0° C. and the aqueous layer was extracted with DCM. The combined organic layers was washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified by silica gel column chromat...

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Abstract

The present invention provides novel compounds of Formula (I), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labeled derivatives, prodrugs, and compositions thereof. Also provided are methods and kits involving the inventive compounds or compositions for treating or preventing proliferative diseases (e.g., cancers (e.g., lung cancer, breast cancer, leukemia, lymphoma, melanoma, multiple myeloma, Ewing's sarcoma, osteosarcoma, brain cancer, neuroblastoma), benign neoplasms, angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases) in a subject. Treatment of a subject with a proliferative disease using a compound or composition of the invention may inhibit the aberrant activity of a kinase (e.g. a protein kinase (e.g. a cyclin-dependent kinase (CDK) (e.g. CDK7, CDK12, or CDK13) or a lipid kinase such as a phosphatidylinositol-5-phosphate 4-kinase (PIP4K) (e.g., PI5P4Kα, PI5P4Kβ, or PI5P4Kγ)) in the subject.

Description

RELATED APPLICATION[0001]The present application claims priority under 35 U.S.C. § 119(e) to U.S. provisional application, U.S. Ser. No. 62 / 185,366, filed Jun. 26, 2015, which is incorporated herein by reference.GOVERNMENT SUPPORT[0002]This invention was made with government support under grant number R01CA197329 awarded by The National Institutes of Health. The government has certain rights in the invention.BACKGROUND OF THE INVENTION[0003]Lung cancer is the leading cancer killer worldwide accounting for 1.37 million deaths annually. In the United States, lung cancer causes more deaths than the next three most common cancers combined (colon, breast and pancreatic) and in 2014, an estimated 159,260 Americans will die from lung cancer. Lung cancer arises as a result of environmental exposures, such as smoking, combined with genetic alterations such as deregulation of oncoproteins, including Myc and RAS, and loss of tumor suppressors, such as p53. The vast majority of patients that de...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/519A61K31/437A61K31/34A61K31/381A61K31/166A61K31/167A61K45/06C07D491/048C07D495/04C07D519/00
CPCA61K31/519A61K31/437A61K31/34A61K31/381C07D519/00A61K31/167A61K45/06C07D491/048C07D495/04A61K31/166A61P35/02A61K2300/00
Inventor GRAY, NATHANAEL S.ZHANG, TINGHU
Owner DANA FARBER CANCER INST INC
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