CO6251317A2 - Procedimiento para sintetizar sal diclorhidrato de ((1s)-1-(((2s) sal diclorhidrato de ((1s)-1-(((2s)-2-(5-(4'-(2-((2s)-1-((2s)-2-((metoxicarbonil)amino)-3-metilbutanoil)-2-pirrolidinil)-1h-imidazol-5-il)-4-bifenilil)-1h-imidazol-2-il)-1-pirrolidinil - Google Patents
Procedimiento para sintetizar sal diclorhidrato de ((1s)-1-(((2s) sal diclorhidrato de ((1s)-1-(((2s)-2-(5-(4'-(2-((2s)-1-((2s)-2-((metoxicarbonil)amino)-3-metilbutanoil)-2-pirrolidinil)-1h-imidazol-5-il)-4-bifenilil)-1h-imidazol-2-il)-1-pirrolidinilInfo
- Publication number
- CO6251317A2 CO6251317A2 CO10009492A CO10009492A CO6251317A2 CO 6251317 A2 CO6251317 A2 CO 6251317A2 CO 10009492 A CO10009492 A CO 10009492A CO 10009492 A CO10009492 A CO 10009492A CO 6251317 A2 CO6251317 A2 CO 6251317A2
- Authority
- CO
- Colombia
- Prior art keywords
- imidazol
- pirrolidinil
- salt
- alkyl
- synthesizing
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 150000003839 salts Chemical class 0.000 title abstract 3
- -1 AMINO Chemical class 0.000 title abstract 2
- 230000002194 synthesizing effect Effects 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 101100439662 Arabidopsis thaliana CHR5 gene Proteins 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000008896 Opium Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical class OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229960001027 opium Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P31/14—Antivirals for RNA viruses
Abstract
La presente revelación se refiere de forma general a un procedimiento para sintetizar sal diclorhidrato de ((1S)-1-(((2S)-2-(5-(4'-(2-((2S)-1-((2S)-2- ((metoxicarbonil)amino)-3-metilbutanoil)-2-pirrolidinil)-1H-imidazol-5-il)-4-bifenilil)-1H-imidazol-2-il)-1-pirrolidinil) carbonil)-2-metilpropicarbamato de metilo. La presente revelación también se refiere de forma general a intermedios útiles en este procedimiento. 1.- Un procedimiento para preparar un compuesto de fórmula (7)o una de sus sales farmacéuticamente aceptable; en la quen es 0,1 ó 2; s es 0, 1, 2, 3 ó 4; u y v se selecciona cada uno independientemente de 0, 1, 2 ó 3; X se selecciona de O, S, S(O), SO2, CH2, CHR5 y C(R5)2; con la condición de que cuando n es 0, X se selecciona de CH2, CHR5 y C(R5)2; R1 y R2 se selecciona cada uno independientemente de alcoxi, alquilo y halo; y cuando s es 2, 3 ó 4, cada R5 en el anillo se selecciona independientemente de alcoxi, alquilo y arilo, donde el alquilo puede formar opcionalmente un anillo condensado de tres a seis miembros con un átomo de carbono adyacente, estando el anillo de tres a seis miembros opcionalmente sustituido con uno o dos grupos alquilo; con la condición de que los dos anillos heterocíclicos que sustituyen los anillos imidazol son idénticos;comprendiendo el procedimiento: (a) hacer reaccionar un compuesto de fórmula (3)en la que u, v, R1 y R2 son como se describen para la fórmula (7); y ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95459507P | 2007-08-08 | 2007-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO6251317A2 true CO6251317A2 (es) | 2011-02-21 |
Family
ID=39865546
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO10009492A CO6251317A2 (es) | 2007-08-08 | 2010-01-29 | Procedimiento para sintetizar sal diclorhidrato de ((1s)-1-(((2s) sal diclorhidrato de ((1s)-1-(((2s)-2-(5-(4'-(2-((2s)-1-((2s)-2-((metoxicarbonil)amino)-3-metilbutanoil)-2-pirrolidinil)-1h-imidazol-5-il)-4-bifenilil)-1h-imidazol-2-il)-1-pirrolidinil |
Country Status (25)
Country | Link |
---|---|
US (1) | US7728027B2 (es) |
EP (1) | EP2178863B1 (es) |
JP (2) | JP5324574B2 (es) |
KR (1) | KR101528542B1 (es) |
CN (1) | CN101778841B (es) |
AR (2) | AR067896A1 (es) |
AU (1) | AU2008284097B2 (es) |
BR (1) | BRPI0815611B1 (es) |
CA (1) | CA2695711C (es) |
CL (1) | CL2008002355A1 (es) |
CO (1) | CO6251317A2 (es) |
CY (1) | CY1113547T1 (es) |
DK (1) | DK2178863T3 (es) |
EA (1) | EA017173B1 (es) |
ES (1) | ES2396267T3 (es) |
HK (1) | HK1137454A1 (es) |
HR (1) | HRP20120990T1 (es) |
IL (1) | IL203685A (es) |
MX (1) | MX2010001415A (es) |
PE (1) | PE20090611A1 (es) |
PL (1) | PL2178863T3 (es) |
PT (1) | PT2178863E (es) |
SI (1) | SI2178863T1 (es) |
TW (1) | TWI423963B (es) |
WO (1) | WO2009020825A1 (es) |
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CN106256825A (zh) * | 2016-07-04 | 2016-12-28 | 四川同晟生物医药有限公司 | 达卡他韦的合成方法 |
WO2018007984A1 (en) * | 2016-07-08 | 2018-01-11 | Lupin Limited | Crystalline forms of daclatasvir dihydrochloride |
CN106432204A (zh) * | 2016-09-12 | 2017-02-22 | 上海步越化工科技有限公司 | 一种抗丙肝达卡他韦的合成方法 |
CN106496199A (zh) * | 2016-10-19 | 2017-03-15 | 上海博志研新药物技术有限公司 | 达卡他韦及其中间体的制备方法 |
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CN109305962B (zh) * | 2017-07-28 | 2022-01-18 | 扬子江药业集团有限公司 | 一种盐酸达拉他韦的精制方法 |
CN107501243A (zh) * | 2017-09-08 | 2017-12-22 | 安徽灵药业有限公司 | 一种达卡他韦的合成方法 |
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IL83467A0 (en) * | 1986-08-15 | 1988-01-31 | Fujisawa Pharmaceutical Co | Imidazole derivatives,processes for their preparation and pharmaceutical compositions containing the same |
EP0679153A4 (en) | 1993-01-14 | 1996-05-15 | Magainin Pharma | FINALLY MODIFIED AMINO ACIDS AND PEPTIDES. |
US5654451B1 (en) | 1993-01-14 | 2000-02-22 | Magainin Pharma | Amino acids and peptides having modified c-terminals and modified n-terminals |
EP1532118A2 (en) * | 2002-07-05 | 2005-05-25 | Axxima Pharmaceuticals Aktiengesellschaft | Imidazole compounds for the treatment of hepatitis c virus infections |
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US8143288B2 (en) | 2005-06-06 | 2012-03-27 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
JP2009508835A (ja) | 2005-09-16 | 2009-03-05 | アロー セラピューティクス リミテッド | ビフェニル誘導体及びc型肝炎の治療におけるその使用 |
WO2007058384A1 (en) | 2005-11-17 | 2007-05-24 | Osaka University | Method of suppressing replication of hepatitis c virus, inhibitor of replication of the virus and method of screening for the same |
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BRPI0712806A2 (pt) | 2006-05-30 | 2012-10-23 | Arrow Therapeutics Ltd | uso de um composto, derivado de bifenila ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, produto, e, método para melhorar uma infecção por hepatite c em um paciente |
US7759495B2 (en) | 2006-08-11 | 2010-07-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8329159B2 (en) * | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7659270B2 (en) | 2006-08-11 | 2010-02-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2008133753A2 (en) | 2006-12-20 | 2008-11-06 | Abbott Laboratories | Anti-viral compounds |
US7728027B2 (en) * | 2007-08-08 | 2010-06-01 | Bristol-Myers Squibb Company | Process for synthesizing compounds useful for treating hepatitis C |
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