JP2005506380A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005506380A5 JP2005506380A5 JP2003538120A JP2003538120A JP2005506380A5 JP 2005506380 A5 JP2005506380 A5 JP 2005506380A5 JP 2003538120 A JP2003538120 A JP 2003538120A JP 2003538120 A JP2003538120 A JP 2003538120A JP 2005506380 A5 JP2005506380 A5 JP 2005506380A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- alkyl
- optionally substituted
- hydroxide
- 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.)
- Withdrawn
Links
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 claims 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical group C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 claims 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N binaphthyl group Chemical group C1(=CC=CC2=CC=CC=C12)C1=CC=CC2=CC=CC=C12 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 claims 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- -1 diphenylphosphino Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims 1
- 150000004692 metal hydroxides Chemical class 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical group Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 claims 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0125442.4A GB0125442D0 (en) | 2001-10-23 | 2001-10-23 | Novel process |
| PCT/GB2002/004459 WO2003035604A1 (en) | 2001-10-23 | 2002-10-02 | Process for the preparation of aryl hydrazone and aryl hydrazine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005506380A JP2005506380A (ja) | 2005-03-03 |
| JP2005506380A5 true JP2005506380A5 (enExample) | 2006-01-05 |
Family
ID=9924372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003538120A Withdrawn JP2005506380A (ja) | 2001-10-23 | 2002-10-02 | 新規プロセス |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7138548B2 (enExample) |
| EP (1) | EP1440053A1 (enExample) |
| JP (1) | JP2005506380A (enExample) |
| CA (1) | CA2463261A1 (enExample) |
| GB (1) | GB0125442D0 (enExample) |
| WO (1) | WO2003035604A1 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1863752A (zh) * | 2002-08-02 | 2006-11-15 | 罗迪亚药业公司 | 铜催化的芳基化 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6235936B1 (en) * | 1998-02-26 | 2001-05-22 | Massachusetts Institute Of Technology | Metal-catalyzed arylations of hydrazines, hydrazones, and related substrates |
-
2001
- 2001-10-23 GB GBGB0125442.4A patent/GB0125442D0/en not_active Ceased
-
2002
- 2002-10-02 EP EP02762609A patent/EP1440053A1/en not_active Withdrawn
- 2002-10-02 JP JP2003538120A patent/JP2005506380A/ja not_active Withdrawn
- 2002-10-02 CA CA002463261A patent/CA2463261A1/en not_active Abandoned
- 2002-10-02 US US10/493,503 patent/US7138548B2/en not_active Expired - Fee Related
- 2002-10-02 WO PCT/GB2002/004459 patent/WO2003035604A1/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2004182741A5 (enExample) | ||
| JP4634560B2 (ja) | 光学活性なインドリン誘導体の製造方法およびその製造中間体 | |
| JP2005053931A5 (enExample) | ||
| JP2010510976A5 (enExample) | ||
| CN1052666A (zh) | 1-苯基-咪唑啉-2,5-二酮衍生物的制备方法 | |
| JP2004522706A5 (enExample) | ||
| JP2004533479A5 (enExample) | ||
| JP2001261662A5 (enExample) | ||
| JP2007526383A5 (enExample) | ||
| JP2004051592A5 (enExample) | ||
| RU2005108973A (ru) | Способ энантиоселективного гидрирования аминоспиртов | |
| JP2006523626A5 (enExample) | ||
| JP2005506380A5 (enExample) | ||
| CN102153434B (zh) | 一种制备芳基酮的方法 | |
| CN1197864C (zh) | 吡唑并哒嗪衍生物的制备方法 | |
| JP2004517891A5 (enExample) | ||
| JP2005508320A5 (enExample) | ||
| CN1930124A (zh) | 制备交叉偶联吲哚的方法 | |
| JP2003261506A5 (enExample) | ||
| JP2007048462A5 (enExample) | ||
| RU2005115255A (ru) | Способ получения индан-1,3-дикарбоновой кислоты | |
| JP2007503406A5 (enExample) | ||
| JP2006509087A5 (enExample) | ||
| JP2005536557A5 (enExample) | ||
| CN1179791C (zh) | 亚膦酰胺和过渡金属的络合物催化剂、合成方法及其在c-c、c-n键形成反应中的用途 |