JP2019517487A5 - - Google Patents
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- JP2019517487A5 JP2019517487A5 JP2018562312A JP2018562312A JP2019517487A5 JP 2019517487 A5 JP2019517487 A5 JP 2019517487A5 JP 2018562312 A JP2018562312 A JP 2018562312A JP 2018562312 A JP2018562312 A JP 2018562312A JP 2019517487 A5 JP2019517487 A5 JP 2019517487A5
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- JP
- Japan
- Prior art keywords
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- compound
- alkyl
- hydroxy
- halo
- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims 39
- 125000000217 alkyl group Chemical group 0.000 claims 25
- 125000005843 halogen group Chemical group 0.000 claims 22
- 239000008194 pharmaceutical composition Substances 0.000 claims 18
- 125000003118 aryl group Chemical group 0.000 claims 16
- 229910052799 carbon Inorganic materials 0.000 claims 16
- 125000001072 heteroaryl group Chemical group 0.000 claims 16
- 125000003282 alkyl amino group Chemical group 0.000 claims 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 14
- 125000003545 alkoxy group Chemical group 0.000 claims 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims 13
- 125000004103 aminoalkyl group Chemical group 0.000 claims 12
- 125000005842 heteroatom Chemical group 0.000 claims 11
- 229910052760 oxygen Inorganic materials 0.000 claims 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 11
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- -1 hydroxy, amino Chemical group 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 229910052717 sulfur Inorganic materials 0.000 claims 10
- 201000010099 disease Diseases 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 8
- 125000004663 dialkyl amino group Chemical group 0.000 claims 8
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 6
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 6
- 206010028980 Neoplasm Diseases 0.000 claims 6
- 201000011510 cancer Diseases 0.000 claims 6
- 101001087416 Homo sapiens Tyrosine-protein phosphatase non-receptor type 11 Proteins 0.000 claims 5
- 102100033019 Tyrosine-protein phosphatase non-receptor type 11 Human genes 0.000 claims 5
- 125000003368 amide group Chemical group 0.000 claims 5
- 150000001721 carbon Chemical group 0.000 claims 5
- 206010006187 Breast cancer Diseases 0.000 claims 3
- 208000026310 Breast neoplasm Diseases 0.000 claims 3
- 206010009944 Colon cancer Diseases 0.000 claims 3
- 208000005101 LEOPARD Syndrome Diseases 0.000 claims 3
- 206010062901 Multiple lentigines syndrome Diseases 0.000 claims 3
- 206010029748 Noonan syndrome Diseases 0.000 claims 3
- 208000010708 Noonan syndrome with multiple lentigines Diseases 0.000 claims 3
- 208000029742 colonic neoplasm Diseases 0.000 claims 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 3
- 208000032839 leukemia Diseases 0.000 claims 3
- 201000001441 melanoma Diseases 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 230000001668 ameliorated effect Effects 0.000 claims 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 230000035772 mutation Effects 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 C*#CC(CCC1)C1(CC1)CCN1c1cnc(c(-c(ccnc2)c2Cl)n[n]2)c2n1 Chemical compound C*#CC(CCC1)C1(CC1)CCN1c1cnc(c(-c(ccnc2)c2Cl)n[n]2)c2n1 0.000 description 3
- IEUPVYYCTFCLTF-UHFFFAOYSA-N CC(CC1)(CCN1c1cnc(c(-c(cc2)cc(Cl)c2Cl)n[nH]2)c2n1)N Chemical compound CC(CC1)(CCN1c1cnc(c(-c(cc2)cc(Cl)c2Cl)n[nH]2)c2n1)N IEUPVYYCTFCLTF-UHFFFAOYSA-N 0.000 description 1
- QKNOZCPUZKQEHX-UHFFFAOYSA-N CC(CC1)(CCN1c1cnc(c(-c2cccc(F)c2Cl)n[nH]2)c2n1)N Chemical compound CC(CC1)(CCN1c1cnc(c(-c2cccc(F)c2Cl)n[nH]2)c2n1)N QKNOZCPUZKQEHX-UHFFFAOYSA-N 0.000 description 1
- FIDMRKBBOFQQJM-UHFFFAOYSA-N CC(CC1)(CCN1c1nc(N)c(C(c(cccn2)c2Cl)=N)nc1)N Chemical compound CC(CC1)(CCN1c1nc(N)c(C(c(cccn2)c2Cl)=N)nc1)N FIDMRKBBOFQQJM-UHFFFAOYSA-N 0.000 description 1
- HILFUTGZGNSLCF-UHFFFAOYSA-N CC(CC1)(CCN1c1nc([nH]nc2-c(cc3)cc(Cl)c3F)c2nc1)N Chemical compound CC(CC1)(CCN1c1nc([nH]nc2-c(cc3)cc(Cl)c3F)c2nc1)N HILFUTGZGNSLCF-UHFFFAOYSA-N 0.000 description 1
- MGGGLWKKMYVXPD-UHFFFAOYSA-N CC(CC1)(CCN1c1nc([nH]nc2-c(cc3)ccc3Cl)c2nc1)N Chemical compound CC(CC1)(CCN1c1nc([nH]nc2-c(cc3)ccc3Cl)c2nc1)N MGGGLWKKMYVXPD-UHFFFAOYSA-N 0.000 description 1
- JQWPQEJDTUKOCS-UHFFFAOYSA-N CC(CC1)(CCN1c1nc([nH]nc2-c(cccc3)c3Cl)c2nc1)N Chemical compound CC(CC1)(CCN1c1nc([nH]nc2-c(cccc3)c3Cl)c2nc1)N JQWPQEJDTUKOCS-UHFFFAOYSA-N 0.000 description 1
- HXKDFUSJAFLWKF-UHFFFAOYSA-N CC(CN)(CC1)CCN1c1cnc(c(-c(cc2)cc(Cl)c2F)n[nH]2)c2n1 Chemical compound CC(CN)(CC1)CCN1c1cnc(c(-c(cc2)cc(Cl)c2F)n[nH]2)c2n1 HXKDFUSJAFLWKF-UHFFFAOYSA-N 0.000 description 1
- BHDQDMSKLZFAOP-UHFFFAOYSA-N CC(CN)(CC1)CCN1c1nc([nH]nc2-c(cc3)ccc3Cl)c2nc1 Chemical compound CC(CN)(CC1)CCN1c1nc([nH]nc2-c(cc3)ccc3Cl)c2nc1 BHDQDMSKLZFAOP-UHFFFAOYSA-N 0.000 description 1
- VBWUNPVCLSZAAP-UHFFFAOYSA-N CC(CN)(CC1)CCN1c1nc([nH]nc2-c3cc(C(F)(F)F)ccc3)c2nc1 Chemical compound CC(CN)(CC1)CCN1c1nc([nH]nc2-c3cc(C(F)(F)F)ccc3)c2nc1 VBWUNPVCLSZAAP-UHFFFAOYSA-N 0.000 description 1
- DEVWTTPPKFBRGL-UHFFFAOYSA-N Clc(cccc1)c1-c1n[nH]c2c1ncc(N1CCC3(CCCC3)CC1)n2 Chemical compound Clc(cccc1)c1-c1n[nH]c2c1ncc(N1CCC3(CCCC3)CC1)n2 DEVWTTPPKFBRGL-UHFFFAOYSA-N 0.000 description 1
- KQCBXUUPBHKHKB-UHFFFAOYSA-N FC(CC1)(CC1(CC1)CCN1c1nc([nH]nc2-c3cccc(Cl)c3Cl)c2nc1)F Chemical compound FC(CC1)(CC1(CC1)CCN1c1nc([nH]nc2-c3cccc(Cl)c3Cl)c2nc1)F KQCBXUUPBHKHKB-UHFFFAOYSA-N 0.000 description 1
- AKZKUGUQZMUCJC-UHFFFAOYSA-N NC(CCC1)C1(CC1)CCN1c1nc([nH]nc2-c(cccc3Cl)c3Cl)c2nc1 Chemical compound NC(CCC1)C1(CC1)CCN1c1nc([nH]nc2-c(cccc3Cl)c3Cl)c2nc1 AKZKUGUQZMUCJC-UHFFFAOYSA-N 0.000 description 1
- KCRBJSWWABFQLC-UHFFFAOYSA-N NC(CF)(CC1)CCN1c1nc([nH]nc2-c3cccc(Cl)c3Cl)c2nc1 Chemical compound NC(CF)(CC1)CCN1c1nc([nH]nc2-c3cccc(Cl)c3Cl)c2nc1 KCRBJSWWABFQLC-UHFFFAOYSA-N 0.000 description 1
- DCZHDAUEYSJCLK-UHFFFAOYSA-N NC(CO)(CC1)CCN1c1cnc(c(-c(cccc2)c2Cl)n[nH]2)c2n1 Chemical compound NC(CO)(CC1)CCN1c1cnc(c(-c(cccc2)c2Cl)n[nH]2)c2n1 DCZHDAUEYSJCLK-UHFFFAOYSA-N 0.000 description 1
- YCRNZPYPOFXDCB-UHFFFAOYSA-N NC(CO)(CC1)CCN1c1cnc(c(-c2cccc(Cl)c2Cl)n[nH]2)c2n1 Chemical compound NC(CO)(CC1)CCN1c1cnc(c(-c2cccc(Cl)c2Cl)n[nH]2)c2n1 YCRNZPYPOFXDCB-UHFFFAOYSA-N 0.000 description 1
- FHEXWCNTNTWBTH-UHFFFAOYSA-N NC(CO)(CC1)CCN1c1cnc(c(-c2cccc(F)c2Cl)n[nH]2)c2n1 Chemical compound NC(CO)(CC1)CCN1c1cnc(c(-c2cccc(F)c2Cl)n[nH]2)c2n1 FHEXWCNTNTWBTH-UHFFFAOYSA-N 0.000 description 1
- XVECDRYVLBLJQU-UHFFFAOYSA-N NC(CO)(CC1)CCN1c1nc([nH]nc2-c(cccn3)c3Cl)c2nc1 Chemical compound NC(CO)(CC1)CCN1c1nc([nH]nc2-c(cccn3)c3Cl)c2nc1 XVECDRYVLBLJQU-UHFFFAOYSA-N 0.000 description 1
- OLCQKOFQXXDERP-UHFFFAOYSA-N NCC(CC1)(CCN1c1nc([nH]nc2-c(c(F)ccc3)c3Cl)c2nc1)O Chemical compound NCC(CC1)(CCN1c1nc([nH]nc2-c(c(F)ccc3)c3Cl)c2nc1)O OLCQKOFQXXDERP-UHFFFAOYSA-N 0.000 description 1
- YMDXJDQSJVLAPR-UHFFFAOYSA-N NCC(CC1)(CCN1c1nc([nH]nc2-c(cccc3)c3Cl)c2nc1)O Chemical compound NCC(CC1)(CCN1c1nc([nH]nc2-c(cccc3)c3Cl)c2nc1)O YMDXJDQSJVLAPR-UHFFFAOYSA-N 0.000 description 1
- FKZOMXXYVRQPKU-CYBMUJFWSA-N N[C@H](CCC1)C1(CC1)CCN1c1cnc(c(-c(cccn2)c2Cl)n[nH]2)c2n1 Chemical compound N[C@H](CCC1)C1(CC1)CCN1c1cnc(c(-c(cccn2)c2Cl)n[nH]2)c2n1 FKZOMXXYVRQPKU-CYBMUJFWSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662343455P | 2016-05-31 | 2016-05-31 | |
| US62/343,455 | 2016-05-31 | ||
| US201762451432P | 2017-01-27 | 2017-01-27 | |
| US62/451,432 | 2017-01-27 | ||
| PCT/US2017/034806 WO2017210134A1 (en) | 2016-05-31 | 2017-05-26 | Heterocyclic inhibitors of ptpn11 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019517487A JP2019517487A (ja) | 2019-06-24 |
| JP2019517487A5 true JP2019517487A5 (cg-RX-API-DMAC10.html) | 2020-07-02 |
| JP7044375B2 JP7044375B2 (ja) | 2022-03-30 |
Family
ID=60420381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018562312A Active JP7044375B2 (ja) | 2016-05-31 | 2017-05-26 | Ptpn11の複素環式阻害剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US10280171B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP3463343B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP7044375B2 (cg-RX-API-DMAC10.html) |
| CN (1) | CN109475531B (cg-RX-API-DMAC10.html) |
| AU (1) | AU2017274199B2 (cg-RX-API-DMAC10.html) |
| CA (1) | CA3024706A1 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2017210134A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11466017B2 (en) | 2011-03-10 | 2022-10-11 | Board Of Regents, The University Of Texas System | Heterocyclic inhibitors of PTPN11 |
| JO3517B1 (ar) | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2 |
| HUE055031T2 (hu) | 2015-12-10 | 2021-10-28 | Ptc Therapeutics Inc | Módszerek Huntington-kór kezelésére |
| JP7044375B2 (ja) | 2016-05-31 | 2022-03-30 | ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム | Ptpn11の複素環式阻害剤 |
| KR20210141778A (ko) | 2016-06-07 | 2021-11-23 | 자코바이오 파마슈티칼스 컴퍼니 리미티드 | Shp2 억제제로서 유용한 신규한 헤테로환형 유도체 |
| RU2744988C2 (ru) | 2016-06-14 | 2021-03-17 | Новартис Аг | Соединения и композиции для подавления активности shp2 |
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