WO2010083645A1 - Pyrimido[5,4-e][1,2,4]triazines et leurs utilisations - Google Patents
Pyrimido[5,4-e][1,2,4]triazines et leurs utilisations Download PDFInfo
- Publication number
- WO2010083645A1 WO2010083645A1 PCT/CN2009/070252 CN2009070252W WO2010083645A1 WO 2010083645 A1 WO2010083645 A1 WO 2010083645A1 CN 2009070252 W CN2009070252 W CN 2009070252W WO 2010083645 A1 WO2010083645 A1 WO 2010083645A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pyrimido
- triazin
- phenyl
- fluoro
- amine
- Prior art date
Links
- 0 CN(*)c1ncc2N=C(*)NNc2n1 Chemical compound CN(*)c1ncc2N=C(*)NNc2n1 0.000 description 3
- XQUAEIRGVKSWCJ-UHFFFAOYSA-N CC(N(CC1)CCN1c1nc(NCc2ccccc2)nc2nnc(-c(cc3)ccc3F)nc12)=O Chemical compound CC(N(CC1)CCN1c1nc(NCc2ccccc2)nc2nnc(-c(cc3)ccc3F)nc12)=O XQUAEIRGVKSWCJ-UHFFFAOYSA-N 0.000 description 1
- BCQOZSBCMDCGNE-UHFFFAOYSA-N CC(Nc(cc1)ccc1-c1nc(c(N2CCOCC2)nc(NCc2ccccc2)n2)c2nn1)=O Chemical compound CC(Nc(cc1)ccc1-c1nc(c(N2CCOCC2)nc(NCc2ccccc2)n2)c2nn1)=O BCQOZSBCMDCGNE-UHFFFAOYSA-N 0.000 description 1
- XOZNGDMLFBOQKM-UHFFFAOYSA-N CCC(CC=C1N=C(c2ccccc2)N=NC1=N1)=C1OC Chemical compound CCC(CC=C1N=C(c2ccccc2)N=NC1=N1)=C1OC XOZNGDMLFBOQKM-UHFFFAOYSA-N 0.000 description 1
- OBRWAXOUVSRMMB-UHFFFAOYSA-N CCOc1nc(NC(C)C)nc2c1nc(-c(cc1)ccc1F)nn2 Chemical compound CCOc1nc(NC(C)C)nc2c1nc(-c(cc1)ccc1F)nn2 OBRWAXOUVSRMMB-UHFFFAOYSA-N 0.000 description 1
- UUQIFGJUOMZIFI-UHFFFAOYSA-N CCOc1nc(NCc(cc2)ccc2F)nc2c1nc(-c(cc1)ccc1F)nn2 Chemical compound CCOc1nc(NCc(cc2)ccc2F)nc2c1nc(-c(cc1)ccc1F)nn2 UUQIFGJUOMZIFI-UHFFFAOYSA-N 0.000 description 1
- VZXRJJWWHVAPLM-UHFFFAOYSA-N CCOc1nc(NCc2ccccc2)nc2c1nc(-c(cc1)cc(OC)c1OC)nn2 Chemical compound CCOc1nc(NCc2ccccc2)nc2c1nc(-c(cc1)cc(OC)c1OC)nn2 VZXRJJWWHVAPLM-UHFFFAOYSA-N 0.000 description 1
- OEISHKHDHXLPGR-UHFFFAOYSA-N COC(NC1=O)=Nc2c1nc(-c1ccccc1)nn2 Chemical compound COC(NC1=O)=Nc2c1nc(-c1ccccc1)nn2 OEISHKHDHXLPGR-UHFFFAOYSA-N 0.000 description 1
- PZFWKOHYDQBQOZ-UHFFFAOYSA-N COc(c(OC)c1)ccc1-c1nc(c(NCc(cc2)ccc2F)nc(NCc(cc2)ccc2F)n2)c2nn1 Chemical compound COc(c(OC)c1)ccc1-c1nc(c(NCc(cc2)ccc2F)nc(NCc(cc2)ccc2F)n2)c2nn1 PZFWKOHYDQBQOZ-UHFFFAOYSA-N 0.000 description 1
- QNNAIDPDWMBETP-UHFFFAOYSA-N COc(c(OC)c1)ccc1-c1nc(cnc(NCc2ccccc2)n2)c2nn1 Chemical compound COc(c(OC)c1)ccc1-c1nc(cnc(NCc2ccccc2)n2)c2nn1 QNNAIDPDWMBETP-UHFFFAOYSA-N 0.000 description 1
- BRHGBTNXELLIOY-UHFFFAOYSA-N COc(ccc(-c1nc(c(N2CCOCC2)nc(NCc(cc2)ccc2F)n2)c2nn1)c1)c1OC Chemical compound COc(ccc(-c1nc(c(N2CCOCC2)nc(NCc(cc2)ccc2F)n2)c2nn1)c1)c1OC BRHGBTNXELLIOY-UHFFFAOYSA-N 0.000 description 1
- JJWPCUOIJFJZIY-UHFFFAOYSA-N COc1nc(NCc(cc2)ccc2F)nc2c1nc(-c(cc1)ccc1F)nn2 Chemical compound COc1nc(NCc(cc2)ccc2F)nc2c1nc(-c(cc1)ccc1F)nn2 JJWPCUOIJFJZIY-UHFFFAOYSA-N 0.000 description 1
- RAASCGFKKYFVRT-UHFFFAOYSA-N COc1ncc2N=C(c(cc3)ccc3F)NNc2n1 Chemical compound COc1ncc2N=C(c(cc3)ccc3F)NNc2n1 RAASCGFKKYFVRT-UHFFFAOYSA-N 0.000 description 1
- IMHFYECHHIBKLN-UHFFFAOYSA-N Fc(cc1)ccc1C1=Nc2cncnc2NN1 Chemical compound Fc(cc1)ccc1C1=Nc2cncnc2NN1 IMHFYECHHIBKLN-UHFFFAOYSA-N 0.000 description 1
- IDXKWCVHCNTSOG-UHFFFAOYSA-N NS(c1ccc(CNc2nc3nnc(-c(cc4)ccc4F)nc3c(N3CCNCC3)n2)cc1)(=O)=O Chemical compound NS(c1ccc(CNc2nc3nnc(-c(cc4)ccc4F)nc3c(N3CCNCC3)n2)cc1)(=O)=O IDXKWCVHCNTSOG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La présente invention porte sur un composé de la formule (I) ou sur un dérivé, un sel ou un promédicament de qualité pharmaceutique de celui-ci : formule (I). La présente invention porte en outre sur des compositions pharmaceutiques comportant un composé de la formule (I) et sur des procédés de traitement ou de prévention d'infections virales, en particulier d'infections au VHC, par l'administration d'un composé de la formule (I).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CN2009/070252 WO2010083645A1 (fr) | 2009-01-21 | 2009-01-21 | Pyrimido[5,4-e][1,2,4]triazines et leurs utilisations |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CN2009/070252 WO2010083645A1 (fr) | 2009-01-21 | 2009-01-21 | Pyrimido[5,4-e][1,2,4]triazines et leurs utilisations |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2010083645A1 true WO2010083645A1 (fr) | 2010-07-29 |
Family
ID=42355487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2009/070252 WO2010083645A1 (fr) | 2009-01-21 | 2009-01-21 | Pyrimido[5,4-e][1,2,4]triazines et leurs utilisations |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2010083645A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102060782A (zh) * | 2010-11-18 | 2011-05-18 | 孙智华 | 制备氯代嘧啶或其类似物的方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3813393A (en) * | 1971-07-13 | 1974-05-28 | Hoffmann La Roche | Pyrimidotriazines |
CN1610683A (zh) * | 2001-12-27 | 2005-04-27 | 霍夫曼-拉罗奇有限公司 | 作为磷酸酶抑制剂的嘧啶并三嗪 |
-
2009
- 2009-01-21 WO PCT/CN2009/070252 patent/WO2010083645A1/fr active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3813393A (en) * | 1971-07-13 | 1974-05-28 | Hoffmann La Roche | Pyrimidotriazines |
CN1610683A (zh) * | 2001-12-27 | 2005-04-27 | 霍夫曼-拉罗奇有限公司 | 作为磷酸酶抑制剂的嘧啶并三嗪 |
Non-Patent Citations (2)
Title |
---|
D. J. BROWN ET AL.: "Aza-analogues of pteridine. Part VI. some 3-alkyl-5(and 7)-aminopyrimido[5,4-e]-as-triazines and related compounds.", JOURNAL OF THE CHEMICAL SOCIETY, PERKIN TRANSACTIONS 1: ORGANIC AND BIO-ORGANIC CHEMISTRY (1972-1999), vol. 18, 1972, pages 2316 - 19 * |
FRANCO GATTA ET AL.: "Synthesis of 2,8-disubstituted 1,2,4-triazolo[5,1-i]purines.", JOURNAL OF HETEROCYCLIC CHEMISTRY, vol. 31, no. 5, 1994, pages 1171 - 6 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102060782A (zh) * | 2010-11-18 | 2011-05-18 | 孙智华 | 制备氯代嘧啶或其类似物的方法 |
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