JP6077006B2 - ベンゾ複素環式化合物およびその使用 - Google Patents
ベンゾ複素環式化合物およびその使用 Download PDFInfo
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- JP6077006B2 JP6077006B2 JP2014551508A JP2014551508A JP6077006B2 JP 6077006 B2 JP6077006 B2 JP 6077006B2 JP 2014551508 A JP2014551508 A JP 2014551508A JP 2014551508 A JP2014551508 A JP 2014551508A JP 6077006 B2 JP6077006 B2 JP 6077006B2
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- 0 C*(C)(c1ccc(*)cc1)c(c(C(OO)=O)c1*)c(*)c(*=*)c1N Chemical compound C*(C)(c1ccc(*)cc1)c(c(C(OO)=O)c1*)c(*)c(*=*)c1N 0.000 description 15
- PFVVPDXPRXNIEZ-UHFFFAOYSA-N COC(c(c(Nc1ccccc1F)c1F)cc2c1nn[s]2)=O Chemical compound COC(c(c(Nc1ccccc1F)c1F)cc2c1nn[s]2)=O PFVVPDXPRXNIEZ-UHFFFAOYSA-N 0.000 description 2
- NFDVKCYUZSSBCE-UHFFFAOYSA-N C=CCC1(CC1)S(N(c(cc1[s]nnc1c1F)c1N1c(ccc(I)c2)c2F)C1=O)(=O)=O Chemical compound C=CCC1(CC1)S(N(c(cc1[s]nnc1c1F)c1N1c(ccc(I)c2)c2F)C1=O)(=O)=O NFDVKCYUZSSBCE-UHFFFAOYSA-N 0.000 description 1
- WXUDKXVLBAUFGF-UHFFFAOYSA-N COC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O Chemical compound COC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O WXUDKXVLBAUFGF-UHFFFAOYSA-N 0.000 description 1
- MIKWEZUYICJSFZ-UHFFFAOYSA-N COC(c(c(Nc(cccc1)c1F)c1F)cc(SCc(cc2)ccc2OC)c1N)=O Chemical compound COC(c(c(Nc(cccc1)c1F)c1F)cc(SCc(cc2)ccc2OC)c1N)=O MIKWEZUYICJSFZ-UHFFFAOYSA-N 0.000 description 1
- FQXMXSWGYNUGHY-UHFFFAOYSA-N COC(c(c(Nc1ccccc1F)c1F)cc(S)c1N)=O Chemical compound COC(c(c(Nc1ccccc1F)c1F)cc(S)c1N)=O FQXMXSWGYNUGHY-UHFFFAOYSA-N 0.000 description 1
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- WKYDRBJFGHHDOF-UHFFFAOYSA-N COC(c(c(Nc1ccccc1F)c1F)cc(SSc(c(N)c2F)cc(C(OC)=O)c2Nc(cccc2)c2F)c1N)=O Chemical compound COC(c(c(Nc1ccccc1F)c1F)cc(SSc(c(N)c2F)cc(C(OC)=O)c2Nc(cccc2)c2F)c1N)=O WKYDRBJFGHHDOF-UHFFFAOYSA-N 0.000 description 1
- KNLZGHPRJQYIMJ-UHFFFAOYSA-N COC(c(cc(c(N)c1F)SCc2ccccc2)c1Nc1ccccc1F)=O Chemical compound COC(c(cc(c(N)c1F)SCc2ccccc2)c1Nc1ccccc1F)=O KNLZGHPRJQYIMJ-UHFFFAOYSA-N 0.000 description 1
- JVFOJFCPIFTUMY-UHFFFAOYSA-N CSc(cc1F)ccc1Nc(c(C(NOCCO)=O)cc1c2nc[s]1)c2F Chemical compound CSc(cc1F)ccc1Nc(c(C(NOCCO)=O)cc1c2nc[s]1)c2F JVFOJFCPIFTUMY-UHFFFAOYSA-N 0.000 description 1
- LCQFWCJNDNYMLZ-UHFFFAOYSA-N C[BrH][I-]C1=[I]CC1 Chemical compound C[BrH][I-]C1=[I]CC1 LCQFWCJNDNYMLZ-UHFFFAOYSA-N 0.000 description 1
- DWLJDFSKXUHTTP-UHFFFAOYSA-N C[O]=S(C1(CC=C)CC1)(Nc(c(Nc(ccc(I)c1)c1F)c1F)cc2c1nn[s]2)=O Chemical compound C[O]=S(C1(CC=C)CC1)(Nc(c(Nc(ccc(I)c1)c1F)c1F)cc2c1nn[s]2)=O DWLJDFSKXUHTTP-UHFFFAOYSA-N 0.000 description 1
- BNVYRBFYIBCXRD-UHFFFAOYSA-N Cc(cc1F)ccc1Nc(c(C(NOCCOC=C)=O)cc1c2nn[s]1)c2F Chemical compound Cc(cc1F)ccc1Nc(c(C(NOCCOC=C)=O)cc1c2nn[s]1)c2F BNVYRBFYIBCXRD-UHFFFAOYSA-N 0.000 description 1
- KKBPZAXGSWAZHA-UHFFFAOYSA-N O=C(Nc(c1c2F)cc3c2nn[s]3)N1c(c(F)c1)ccc1I Chemical compound O=C(Nc(c1c2F)cc3c2nn[s]3)N1c(c(F)c1)ccc1I KKBPZAXGSWAZHA-UHFFFAOYSA-N 0.000 description 1
- LPHRRQNLJIOSTB-UHFFFAOYSA-N O=C(c(c(Nc(c(Cl)c1)ccc1Br)c1F)cc2c1nc[s]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(c(Cl)c1)ccc1Br)c1F)cc2c1nc[s]2)NOCC1CC1 LPHRRQNLJIOSTB-UHFFFAOYSA-N 0.000 description 1
- LCQLPQKOKHKAAP-UHFFFAOYSA-N O=C(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)NOCC1CC1 LCQLPQKOKHKAAP-UHFFFAOYSA-N 0.000 description 1
- CCTFDOJAXGVCHD-UHFFFAOYSA-N O=C(c(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)NOCC1CC1 Chemical compound O=C(c(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)NOCC1CC1 CCTFDOJAXGVCHD-UHFFFAOYSA-N 0.000 description 1
- JUUINOLJRQVJJV-UHFFFAOYSA-N OC(c(c(Nc(cccc1)c1F)c1F)cc(Br)c1F)=O Chemical compound OC(c(c(Nc(cccc1)c1F)c1F)cc(Br)c1F)=O JUUINOLJRQVJJV-UHFFFAOYSA-N 0.000 description 1
- UQXIRWMDNLQNGM-UHFFFAOYSA-N OC(c(cc(c(F)c1F)OCc2ccccc2)c1Nc1ccccc1F)=O Chemical compound OC(c(cc(c(F)c1F)OCc2ccccc2)c1Nc1ccccc1F)=O UQXIRWMDNLQNGM-UHFFFAOYSA-N 0.000 description 1
- IVGFMRMTHAGJIO-UHFFFAOYSA-N OCC(CC1(CC1)S(Nc(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)(=O)=O)O Chemical compound OCC(CC1(CC1)S(Nc(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)(=O)=O)O IVGFMRMTHAGJIO-UHFFFAOYSA-N 0.000 description 1
- YYSGXYRHKZCROD-UHFFFAOYSA-N OCC(CC1(CCC1)S(Nc(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)(=O)=O)O Chemical compound OCC(CC1(CCC1)S(Nc(c(Nc(ccc(Br)c1)c1Cl)c1F)cc2c1nc[o]2)(=O)=O)O YYSGXYRHKZCROD-UHFFFAOYSA-N 0.000 description 1
- LMFCHUNAYDSVRN-UHFFFAOYSA-N OCCONC(c(c(NC(C(F)=C1)=CCC1Br)c1F)cc2c1nn[s]2)=O Chemical compound OCCONC(c(c(NC(C(F)=C1)=CCC1Br)c1F)cc2c1nn[s]2)=O LMFCHUNAYDSVRN-UHFFFAOYSA-N 0.000 description 1
- QQVGXTZHZFIFCV-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1Br)c1F)cc2c1nc[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1Br)c1F)cc2c1nc[s]2)=O QQVGXTZHZFIFCV-UHFFFAOYSA-N 0.000 description 1
- KALDBJONLIOQJS-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[o]2)=O KALDBJONLIOQJS-UHFFFAOYSA-N 0.000 description 1
- UFZJUVFSSINETF-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nc[s]2)=O UFZJUVFSSINETF-UHFFFAOYSA-N 0.000 description 1
- NCXQEKULAYAEMA-UHFFFAOYSA-N OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O Chemical compound OCCONC(c(c(Nc(c(F)c1)ccc1I)c1F)cc2c1nn[s]2)=O NCXQEKULAYAEMA-UHFFFAOYSA-N 0.000 description 1
- ZEVWANKJVWLMBU-UHFFFAOYSA-N OCCONC(c(c(Nc(ccc(C(F)(F)F)c1)c1F)c1F)cc2c1nc[o]2)=O Chemical compound OCCONC(c(c(Nc(ccc(C(F)(F)F)c1)c1F)c1F)cc2c1nc[o]2)=O ZEVWANKJVWLMBU-UHFFFAOYSA-N 0.000 description 1
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- 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
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- Health & Medical Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210014021.X | 2012-01-17 | ||
| CN201210014021 | 2012-01-17 | ||
| CN201210189087.2 | 2012-06-08 | ||
| CN201210190520.4 | 2012-06-08 | ||
| CN201210189086.8A CN103204822B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噁唑化合物及其制备方法和用途 |
| CN201210189087.2A CN103204827B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噻二唑化合物及其制备方法和用途 |
| CN201210190520.4A CN103204825B (zh) | 2012-01-17 | 2012-06-08 | 作为蛋白激酶抑制剂的苯并噻唑化合物及其制备方法和用途 |
| CN201210189086.8 | 2012-06-08 | ||
| PCT/CN2013/000037 WO2013107283A1 (en) | 2012-01-17 | 2013-01-16 | Benzoheterocyclic compounds and use thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015503597A JP2015503597A (ja) | 2015-02-02 |
| JP2015503597A5 JP2015503597A5 (enExample) | 2016-03-10 |
| JP6077006B2 true JP6077006B2 (ja) | 2017-02-08 |
Family
ID=48752254
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014551508A Active JP6077006B2 (ja) | 2012-01-17 | 2013-01-16 | ベンゾ複素環式化合物およびその使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9290468B2 (enExample) |
| EP (1) | EP2804855B1 (enExample) |
| JP (1) | JP6077006B2 (enExample) |
| CN (3) | CN103204827B (enExample) |
| CA (1) | CA2897259C (enExample) |
| NZ (1) | NZ627631A (enExample) |
| WO (1) | WO2013107283A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104710417B (zh) * | 2013-12-11 | 2020-09-08 | 上海科州药物研发有限公司 | 氮杂吲哚类衍生物及其合成方法 |
| CN105384738B (zh) * | 2014-08-21 | 2017-08-29 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
| CN105859543A (zh) * | 2016-05-06 | 2016-08-17 | 蚌埠中实化学技术有限公司 | 一种2,6-二氟-4-溴苯甲酰氯的制备方法 |
| CN111205244B (zh) * | 2018-11-22 | 2023-08-18 | 上海科技大学 | 噻唑并环类化合物、其制备方法、中间体和应用 |
| AU2020242287A1 (en) | 2019-03-21 | 2021-09-02 | INSERM (Institut National de la Santé et de la Recherche Médicale) | A Dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| KR20220098759A (ko) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | 키나제 억제제에 대해 내성을 획득한 암의 치료 방법 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
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| CN103204822A (zh) | 2013-07-17 |
| CN103204822B (zh) | 2014-12-03 |
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| AU2013201455B2 (en) | 2015-07-23 |
| US20160235721A1 (en) | 2016-08-18 |
| US9290468B2 (en) | 2016-03-22 |
| CN103204825B (zh) | 2015-03-04 |
| CN103204825A (zh) | 2013-07-17 |
| AU2013201455A8 (en) | 2016-04-14 |
| NZ627631A (en) | 2016-10-28 |
| CN103204827B (zh) | 2014-12-03 |
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| EP2804855A1 (en) | 2014-11-26 |
| EP2804855B1 (en) | 2017-09-20 |
| JP2015503597A (ja) | 2015-02-02 |
| AU2013201455A1 (en) | 2013-08-01 |
| CA2897259C (en) | 2019-05-07 |
| EP2804855A4 (en) | 2015-07-29 |
| US9937158B2 (en) | 2018-04-10 |
| AU2013201455C1 (en) | 2016-01-21 |
| CN103204827A (zh) | 2013-07-17 |
| US20140371278A1 (en) | 2014-12-18 |
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