KR20170132307A - 스피로 고리 화합물 - Google Patents
스피로 고리 화합물 Download PDFInfo
- Publication number
- KR20170132307A KR20170132307A KR1020177031578A KR20177031578A KR20170132307A KR 20170132307 A KR20170132307 A KR 20170132307A KR 1020177031578 A KR1020177031578 A KR 1020177031578A KR 20177031578 A KR20177031578 A KR 20177031578A KR 20170132307 A KR20170132307 A KR 20170132307A
- Authority
- KR
- South Korea
- Prior art keywords
- optionally substituted
- alkyl
- cancer
- compound
- heteroaryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 0 *c1n[n]c2c1cccc2 Chemical compound *c1n[n]c2c1cccc2 0.000 description 8
- KAWWDZCGWPGUDT-LHEWISCISA-N CC(C)Oc(nc1)ccc1-c(c1c2)n[nH]c1ccc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3nnc(C)[o]3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c(c1c2)n[nH]c1ccc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3nnc(C)[o]3)=O)CC1)C2=O KAWWDZCGWPGUDT-LHEWISCISA-N 0.000 description 2
- HIOZECCLUJYAMP-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O HIOZECCLUJYAMP-UHFFFAOYSA-N 0.000 description 2
- DKPAILLVWPRHAF-KDXMTYKHSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c(nc3)ncc3F)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c(nc3)ncc3F)=O)CC1)C2=O DKPAILLVWPRHAF-KDXMTYKHSA-N 0.000 description 2
- HIOZECCLUJYAMP-LHEWISCISA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O HIOZECCLUJYAMP-LHEWISCISA-N 0.000 description 2
- DHZKRRWSSKSLPY-KDXMTYKHSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3ncccn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3ncccn3)=O)CC1)C2=O DHZKRRWSSKSLPY-KDXMTYKHSA-N 0.000 description 2
- IQWWIEPRGZHCFV-OBACSPHBSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCC3C(C3)(C4)CC34c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCC3C(C3)(C4)CC34c3n[n](C)cn3)=O)CC1)C2=O IQWWIEPRGZHCFV-OBACSPHBSA-N 0.000 description 2
- OBQBSLOTUAAHHD-KDXMTYKHSA-N CCNc1nnc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c(cn3)ccc3OC(C)C)C2=O)=O)[o]1 Chemical compound CCNc1nnc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c(cn3)ccc3OC(C)C)C2=O)=O)[o]1 OBQBSLOTUAAHHD-KDXMTYKHSA-N 0.000 description 2
- DNWFIDHHKVXWJV-UMSFTDKQSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4N3CCOCC3)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4N3CCOCC3)C2=O)=O)nc1 DNWFIDHHKVXWJV-UMSFTDKQSA-N 0.000 description 2
- LTLVZQZDXQWLHU-UHFFFAOYSA-N C#Cc(cc1)ccc1Br Chemical compound C#Cc(cc1)ccc1Br LTLVZQZDXQWLHU-UHFFFAOYSA-N 0.000 description 1
- WESHHUYKHJTPMF-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC1)CC11CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1 Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC1)CC11CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1 WESHHUYKHJTPMF-UHFFFAOYSA-N 0.000 description 1
- WEEYVUODPBBECN-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC1)CC11CN(CC(N(CC2)CCN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1 Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC1)CC11CN(CC(N(CC2)CCN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1 WEEYVUODPBBECN-UHFFFAOYSA-N 0.000 description 1
- YOFGTZMWLSMYLJ-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(CC(N(CC3)CCN3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(CC(N(CC3)CCN3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O YOFGTZMWLSMYLJ-UHFFFAOYSA-N 0.000 description 1
- MQXPFLQIWYIPKQ-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(Cc3ccccc3)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CCC12CN(Cc3ccccc3)CC1)C2=O MQXPFLQIWYIPKQ-UHFFFAOYSA-N 0.000 description 1
- VFTPQVWOIRZGNK-KDXMTYKHSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3c[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3c[n](C)cn3)=O)CC1)C2=O VFTPQVWOIRZGNK-KDXMTYKHSA-N 0.000 description 1
- AUYJRJPTGVBQLV-LHEWISCISA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3c[n](C)nn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3c[n](C)nn3)=O)CC1)C2=O AUYJRJPTGVBQLV-LHEWISCISA-N 0.000 description 1
- SFSNWHRVRJIJDQ-LHEWISCISA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ncc3-c3ncccn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CC=C3c(cc3)ncc3-c3ncccn3)=O)CC1)C2=O SFSNWHRVRJIJDQ-LHEWISCISA-N 0.000 description 1
- XTTJGAWTXBNCAU-LHEWISCISA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCC3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCC3c(cc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O XTTJGAWTXBNCAU-LHEWISCISA-N 0.000 description 1
- JRXUENAEZSWQFF-BHVANESWSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCN3c(nc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N(CC[C@]12CN(CC(N(CC3)CCN3c(nc3)ccc3-c3n[n](C)cn3)=O)CC1)C2=O JRXUENAEZSWQFF-BHVANESWSA-N 0.000 description 1
- CCMWYGFUITYBRG-UHFFFAOYSA-O CC(C)Oc(nc1)ccc1C(c(cc(cc1)N(CCC23CN(CC(N(CC4)CC=C4c(cc4)ccc4-c4n[n](C)cn4)=O)C2)C3=O)c1N)=[NH2+] Chemical compound CC(C)Oc(nc1)ccc1C(c(cc(cc1)N(CCC23CN(CC(N(CC4)CC=C4c(cc4)ccc4-c4n[n](C)cn4)=O)C2)C3=O)c1N)=[NH2+] CCMWYGFUITYBRG-UHFFFAOYSA-O 0.000 description 1
- VJOLIAZLNLMHDM-QNGWXLTQSA-N CC(C)Oc(nc1)ccc1C(c(cc(cc1)N(CC[C@]23CN(CC(N(CC4)CC=C4c(cc4)ccc4-[n]4nncc4)=O)CC2)C3=O)c1N)=N Chemical compound CC(C)Oc(nc1)ccc1C(c(cc(cc1)N(CC[C@]23CN(CC(N(CC4)CC=C4c(cc4)ccc4-[n]4nncc4)=O)CC2)C3=O)c1N)=N VJOLIAZLNLMHDM-QNGWXLTQSA-N 0.000 description 1
- OORZQSHEZWPWLO-UHFFFAOYSA-N CCNc1nnc(-c(cc2)ccc2C(CC2)=CCN2C(CCl)=O)[o]1 Chemical compound CCNc1nnc(-c(cc2)ccc2C(CC2)=CCN2C(CCl)=O)[o]1 OORZQSHEZWPWLO-UHFFFAOYSA-N 0.000 description 1
- OCUCNGGDQCLRPV-DHUJRADRSA-P CN/C=N\C(c(cc1)ccc1C(CC1)=CCN1C(CN(CC1)C[C@]1(CCN1c(cc2)cc(C(c3cc(C(F)(F)F)ncc3)=[NH2+])c2N)C1=O)=O)=[NH2+] Chemical compound CN/C=N\C(c(cc1)ccc1C(CC1)=CCN1C(CN(CC1)C[C@]1(CCN1c(cc2)cc(C(c3cc(C(F)(F)F)ncc3)=[NH2+])c2N)C1=O)=O)=[NH2+] OCUCNGGDQCLRPV-DHUJRADRSA-P 0.000 description 1
- OFXJKTLKELRECI-QNGWXLTQSA-O CN/C=N\C(c(cc1)ccc1C(CC1)=CCN1C(CN(CC1)C[C@]1(CCN1c(cc2)cc(C(c3ccnc(C4(CC4)C(F)(F)F)c3)=N)c2N)C1=O)=O)=[NH2+] Chemical compound CN/C=N\C(c(cc1)ccc1C(CC1)=CCN1C(CN(CC1)C[C@]1(CCN1c(cc2)cc(C(c3ccnc(C4(CC4)C(F)(F)F)c3)=N)c2N)C1=O)=O)=[NH2+] OFXJKTLKELRECI-QNGWXLTQSA-O 0.000 description 1
- GUGJZWXFZKJQRD-UHFFFAOYSA-N CN1NNC(c(cc2)ccc2C(CC2)=CCN2C(CCl)=O)=C1 Chemical compound CN1NNC(c(cc2)ccc2C(CC2)=CCN2C(CCl)=O)=C1 GUGJZWXFZKJQRD-UHFFFAOYSA-N 0.000 description 1
- VPIPXJVRKCUWAN-FEXPOBHUSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc(C(C4CC(C(F)(F)F)NCC4)=N)c3N)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc(C(C4CC(C(F)(F)F)NCC4)=N)c3N)C2=O)=O)nc1 VPIPXJVRKCUWAN-FEXPOBHUSA-N 0.000 description 1
- GHDHDWOJWFCONS-DHUJRADRSA-O C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc(C(c4cnccc4C(F)(F)F)=[NH2+])c3N)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc(C(c4cnccc4C(F)(F)F)=[NH2+])c3N)C2=O)=O)nc1 GHDHDWOJWFCONS-DHUJRADRSA-O 0.000 description 1
- WAQBPXZENUSGPV-DHUJRADRSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c3cc(C(F)(F)F)ncc3)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c3cc(C(F)(F)F)ncc3)C2=O)=O)nc1 WAQBPXZENUSGPV-DHUJRADRSA-N 0.000 description 1
- HATSZXFYDINHCW-QNGWXLTQSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c3ccnc(C4(CC4)C(F)(F)F)c3)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc3)cc4c3[nH]nc4-c3ccnc(C4(CC4)C(F)(F)F)c3)C2=O)=O)nc1 HATSZXFYDINHCW-QNGWXLTQSA-N 0.000 description 1
- ZBKKIPOMBSXYDX-PMERELPUSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c3ccc4[nH]ncc4c3)C2=O)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c3ccc4[nH]ncc4c3)C2=O)=O)nc1 ZBKKIPOMBSXYDX-PMERELPUSA-N 0.000 description 1
- YKXDSEQWMNBYPU-UMSFTDKQSA-N C[n]1ncc(-c2n[nH]c(cc3)c2cc3N(CC[C@]23CN(CC(N(CC4)CC=C4c(cc4)ccc4-c4n[n](C)cn4)=O)CC2)C3=O)c1 Chemical compound C[n]1ncc(-c2n[nH]c(cc3)c2cc3N(CC[C@]23CN(CC(N(CC4)CC=C4c(cc4)ccc4-c4n[n](C)cn4)=O)CC2)C3=O)c1 YKXDSEQWMNBYPU-UMSFTDKQSA-N 0.000 description 1
- MZKWDMAXFOJDMI-UHFFFAOYSA-N C[n]1nnc(-c(cc2)ccc2Br)c1 Chemical compound C[n]1nnc(-c(cc2)ccc2Br)c1 MZKWDMAXFOJDMI-UHFFFAOYSA-N 0.000 description 1
- TYEFMUYXGHKDPR-DHUJRADRSA-N Cc1n[o]c(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc34)ccc3[nH]nc4-c3ccnc(C(F)(F)F)c3)C2=O)=O)n1 Chemical compound Cc1n[o]c(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@]2(CCN2c(cc34)ccc3[nH]nc4-c3ccnc(C(F)(F)F)c3)C2=O)=O)n1 TYEFMUYXGHKDPR-DHUJRADRSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
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| US62/142,946 | 2015-04-03 | ||
| PCT/US2016/025345 WO2016161160A1 (en) | 2015-04-03 | 2016-03-31 | Spirocyclic compounds |
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| KR20170048588A (ko) * | 2014-09-17 | 2017-05-08 | 카리라 파마슈티컬스, 아이앤씨. | 바이사이클릭 화합물 |
| DK3277690T3 (da) | 2015-04-03 | 2020-05-04 | Recurium Ip Holdings Llc | Spirocykliske forbindelser |
| BR112019005305A2 (pt) * | 2016-10-05 | 2019-07-02 | Zeno Royalties & Milestones Llc | compostos espirocíclicos |
| WO2018107072A1 (en) | 2016-12-08 | 2018-06-14 | Board Of Regents, The University Of Texas System | Bicyclo[1.1.1]pentane inhibitors of dual leucine zipper (dlk) kinase for the treatment of disease |
| SG11202007251XA (en) * | 2018-01-31 | 2020-08-28 | Aptinyx Inc | Spiro-lactam nmda receptor modulators and uses thereof |
| EP3956330A4 (en) | 2019-04-18 | 2023-01-18 | The Johns Hopkins University | SUBSTITUTED 2-AMINO-PYRAZOLYL-[1,2,4]TRIAZOLO[1,5A]PYRIDINE DERIVATIVES AND THEIR USE |
| US11560366B2 (en) | 2019-10-21 | 2023-01-24 | Board Of Regents, The University Of Texas System | Bicyclo[1.1.1]pentane inhibitors of dual leucine zipper (DLK) kinase for the treatment of disease |
| CN115124542A (zh) * | 2022-07-08 | 2022-09-30 | 河南师范大学 | 羟基苯取代吡唑酮并吲唑[螺]吡唑酮类化合物的合成方法 |
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| AR057579A1 (es) * | 2005-11-23 | 2007-12-05 | Merck & Co Inc | Compuestos espirociclicos como inhibidores de histona de acetilasa (hdac) |
| US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
| EP2086974B1 (en) | 2006-11-17 | 2013-07-24 | Polyera Corporation | Diimide-based semiconductor materials and methods of preparing and using the same |
| SG188179A1 (en) | 2008-02-21 | 2013-03-28 | Merck Sharp & Dohme | Compounds that are erk inhibitors |
| US20110166124A1 (en) | 2008-07-23 | 2011-07-07 | Mccormick Kevin D | Tricyclic spirocycle derivatives and methods of use |
| WO2011041152A1 (en) | 2009-09-30 | 2011-04-07 | Schering Corporation | Novel compounds that are erk inhibitors |
| US9687550B2 (en) | 2009-12-07 | 2017-06-27 | Arbutus Biopharma Corporation | Compositions for nucleic acid delivery |
| EP2751118B1 (en) | 2011-08-29 | 2016-10-12 | Bristol-Myers Squibb Company | Spiro bicyclic diamine derivatives as hiv attachment inhibitors |
| CN103130775B (zh) * | 2011-11-22 | 2015-09-30 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的吲哚满酮衍生物 |
| US8987264B2 (en) * | 2012-11-09 | 2015-03-24 | Bristol-Myers Squibb Company | 1,3,5-triazine derivatives of spiro bicyclic oxalamide-compounds for treatment of hepatitis C |
| JP6506248B2 (ja) * | 2013-03-14 | 2019-04-24 | ゾーン・ロイヤリティズ・アンド・マイルストーンズ・エルエルシー | 二環式鎮痛化合物 |
| CN105732636B (zh) | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
| DK3277690T3 (da) | 2015-04-03 | 2020-05-04 | Recurium Ip Holdings Llc | Spirocykliske forbindelser |
| BR112019005305A2 (pt) | 2016-10-05 | 2019-07-02 | Zeno Royalties & Milestones Llc | compostos espirocíclicos |
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