KR960703916A - 하이메니알디신 및 그의 유도체, 그들의 합성 중간체 제조법 및 그의 합성 중간체(hymenialdisine and derivative thereof, process for producing intermediate for synthesizing the same, and said intermediate) - Google Patents
하이메니알디신 및 그의 유도체, 그들의 합성 중간체 제조법 및 그의 합성 중간체(hymenialdisine and derivative thereof, process for producing intermediate for synthesizing the same, and said intermediate)Info
- Publication number
- KR960703916A KR960703916A KR1019960700258A KR19960700258A KR960703916A KR 960703916 A KR960703916 A KR 960703916A KR 1019960700258 A KR1019960700258 A KR 1019960700258A KR 19960700258 A KR19960700258 A KR 19960700258A KR 960703916 A KR960703916 A KR 960703916A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- formula
- methoxybenzyloxymethyl
- trimethylsilylethoxymethyl
- compound represented
- 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- Withdrawn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
- QPCBNXNDVYOBIP-WHFBIAKZSA-N hymenialdisine Chemical compound NC1=NC(=O)C([C@@H]2[C@@H]3C=C(Br)N=C3C(=O)NCC2)=N1 QPCBNXNDVYOBIP-WHFBIAKZSA-N 0.000 title 1
- ATBAETXFFCOZOY-UHFFFAOYSA-N hymenialdisine Natural products N1C(N)=NC(=O)C1=C1C(C=C(Br)N2)=C2C(=O)NCC1 ATBAETXFFCOZOY-UHFFFAOYSA-N 0.000 title 1
- 230000002194 synthesizing effect Effects 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 claims abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 6
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- -1 trimethylsilylethoxymethyl group Chemical group 0.000 claims 67
- 150000001875 compounds Chemical class 0.000 claims 10
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 8
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 2
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 230000002140 halogenating effect Effects 0.000 claims 1
- 239000007800 oxidant agent Substances 0.000 claims 1
- 102000003923 Protein Kinase C Human genes 0.000 abstract 2
- 108090000315 Protein Kinase C Proteins 0.000 abstract 2
- 230000004913 activation Effects 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10403094A JP3714685B2 (ja) | 1994-05-18 | 1994-05-18 | ハイメニアルディシン及びその誘導体並びにそれらの合成中間体の製造法並びにその合成中間体 |
| JP94-104030 | 1994-11-23 | ||
| PCT/JP1995/000941 WO1995031462A1 (en) | 1994-05-18 | 1995-05-17 | Hymenialdisine and derivative thereof, process for producing intermediate for synthesizing the same, and said intermediate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR960703916A true KR960703916A (ko) | 1996-08-31 |
Family
ID=14369852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019960700258A Withdrawn KR960703916A (ko) | 1994-05-18 | 1995-05-17 | 하이메니알디신 및 그의 유도체, 그들의 합성 중간체 제조법 및 그의 합성 중간체(hymenialdisine and derivative thereof, process for producing intermediate for synthesizing the same, and said intermediate) |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5621099A (enExample) |
| EP (1) | EP0711773B1 (enExample) |
| JP (1) | JP3714685B2 (enExample) |
| KR (1) | KR960703916A (enExample) |
| AU (1) | AU701436B2 (enExample) |
| CA (1) | CA2167515A1 (enExample) |
| DE (1) | DE69522642T2 (enExample) |
| ES (1) | ES2160164T3 (enExample) |
| WO (1) | WO1995031462A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU6557194A (en) * | 1993-04-08 | 1994-11-08 | Trustees Of Columbia University In The City Of New York, The | Method for the synthesis of 4- and/or 5-(di)substituted 2-aminoimidazoles from 2-aminoimidazoles and aldehydes |
| WO1997020845A1 (fr) * | 1995-12-01 | 1997-06-12 | Suntory Limited | Derives de pyrroloazepine |
| CA2216559A1 (en) * | 1997-09-25 | 1999-03-25 | Michel Roberge | G2 checkpoint inhibitors and assay |
| US6197954B1 (en) | 1998-01-30 | 2001-03-06 | The Trustees Of Columbia University In The City Of New York | Intermediates for the synthesis of debromohymenialdisine and processes thereof |
| US6211361B1 (en) * | 1999-07-20 | 2001-04-03 | State Of Oregon Acting By And Through The Oregon State Board Of Higher Education On Behalf Of Oregon, State Univeristy | Method for making debromohymenialdisine and analogs thereof |
| ATE253918T1 (de) * | 1999-12-08 | 2003-11-15 | Centre Nat Rech Scient | Verwendung von hymenialdisin und dessen derivaten zur herstellung therapeutischer mittel |
| AU2968701A (en) * | 2000-01-24 | 2001-07-31 | Genzyme Corporation | Jak/stat pathway inhibitors and the uses thereof |
| AU783615B2 (en) | 2000-05-11 | 2005-11-17 | Consejo Superior De Investigaciones Cientificas | Heterocyclic inhibitors of glycogen synthase kinase GSK-3 |
| AU2003301226A1 (en) * | 2002-12-20 | 2004-07-22 | Pharmacia Corp | Acyclic pyrazole compounds for the inhibition of mitogen activated protein kinase-activated protein kinase-2 |
| US7423031B2 (en) * | 2003-05-01 | 2008-09-09 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| WO2004103958A2 (en) * | 2003-05-19 | 2004-12-02 | Michigan State University | Preparation of hymenialdisine derivatives and use thereof |
| CN115245170B (zh) * | 2021-04-28 | 2024-10-22 | 南开大学 | Aldisin及其生物碱衍生物在防治植物病毒、杀虫、杀菌方面的应用 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62161786A (ja) * | 1986-01-08 | 1987-07-17 | Mitsubishi Chem Ind Ltd | ピロ−ル化合物 |
| US4729996A (en) * | 1986-05-29 | 1988-03-08 | Harbor Branch Oceanographic Institution, Inc. | Antitumor compositions and their methods of use |
| JP3198117B2 (ja) * | 1990-02-07 | 2001-08-13 | サントリー株式会社 | ピロロアゼピン誘導体 |
| US5565448A (en) * | 1992-02-24 | 1996-10-15 | Smithkline Beecham Corporation | Medicament |
-
1994
- 1994-05-18 JP JP10403094A patent/JP3714685B2/ja not_active Expired - Fee Related
-
1995
- 1995-05-17 EP EP95918732A patent/EP0711773B1/en not_active Expired - Lifetime
- 1995-05-17 WO PCT/JP1995/000941 patent/WO1995031462A1/ja not_active Ceased
- 1995-05-17 US US08/586,638 patent/US5621099A/en not_active Expired - Fee Related
- 1995-05-17 KR KR1019960700258A patent/KR960703916A/ko not_active Withdrawn
- 1995-05-17 CA CA002167515A patent/CA2167515A1/en not_active Abandoned
- 1995-05-17 ES ES95918732T patent/ES2160164T3/es not_active Expired - Lifetime
- 1995-05-17 AU AU24541/95A patent/AU701436B2/en not_active Ceased
- 1995-05-17 DE DE69522642T patent/DE69522642T2/de not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0711773A4 (enExample) | 1996-06-19 |
| AU701436B2 (en) | 1999-01-28 |
| AU2454195A (en) | 1995-12-05 |
| JP3714685B2 (ja) | 2005-11-09 |
| EP0711773A1 (en) | 1996-05-15 |
| WO1995031462A1 (en) | 1995-11-23 |
| EP0711773B1 (en) | 2001-09-12 |
| CA2167515A1 (en) | 1995-11-23 |
| ES2160164T3 (es) | 2001-11-01 |
| US5621099A (en) | 1997-04-15 |
| JPH07309874A (ja) | 1995-11-28 |
| DE69522642T2 (de) | 2002-04-18 |
| DE69522642D1 (de) | 2001-10-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 19960118 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |