JP2003518105A5 - - Google Patents
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- Publication number
- JP2003518105A5 JP2003518105A5 JP2001547071A JP2001547071A JP2003518105A5 JP 2003518105 A5 JP2003518105 A5 JP 2003518105A5 JP 2001547071 A JP2001547071 A JP 2001547071A JP 2001547071 A JP2001547071 A JP 2001547071A JP 2003518105 A5 JP2003518105 A5 JP 2003518105A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- cycloalkyl
- particular phenyl
- heterocyclylmethyl
- 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.)
- Granted
Links
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000005842 heteroatoms Chemical group 0.000 description 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
Description
〔式中、
R5は、アルキル、シクロアルキル、アリール、アリールアルキルまたはヘテロシクロアルキルであって、そのそれぞれは置換されていてもよい。
R5は、好ましくはC1〜C10−アルキル、C3〜C10−シクロアルキル、アリール−C1〜C4−アルキル、特にはフェニル−C1〜C4−アルキル、そのそれぞれは一置換または多置換されてもよく、ここで適当な置換基はOH、SH、ハロゲン、C1〜C6−アルコキシ、C1〜C6−アルキルチオ、C1〜C6−アルキルおよびアリール、特にはフェニル、またはヘテロシクリルメチルであって、ここでヘテロシクリルは、窒素、酸素、硫黄の組からのヘテロ原子1個または2個(好ましくは1個)を有する不飽和または飽和の5員または6員複素環、特にはフリル、テトラヒドロフリル、チエニルまたはピリジルである。〕
の化合物を含む。
R5は、アルキル、シクロアルキル、アリール、アリールアルキルまたはヘテロシクロアルキルであって、そのそれぞれは置換されていてもよい。
R5は、好ましくはC1〜C10−アルキル、C3〜C10−シクロアルキル、アリール−C1〜C4−アルキル、特にはフェニル−C1〜C4−アルキル、そのそれぞれは一置換または多置換されてもよく、ここで適当な置換基はOH、SH、ハロゲン、C1〜C6−アルコキシ、C1〜C6−アルキルチオ、C1〜C6−アルキルおよびアリール、特にはフェニル、またはヘテロシクリルメチルであって、ここでヘテロシクリルは、窒素、酸素、硫黄の組からのヘテロ原子1個または2個(好ましくは1個)を有する不飽和または飽和の5員または6員複素環、特にはフリル、テトラヒドロフリル、チエニルまたはピリジルである。〕
の化合物を含む。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19961604.3 | 1999-12-21 | ||
DE19961604A DE19961604A1 (de) | 1999-12-21 | 1999-12-21 | Verfahren zur Herstellung von 1,3-disubstituierten 2-Nitroguanidinen |
PCT/EP2000/012495 WO2001046160A1 (de) | 1999-12-21 | 2000-12-08 | Verfahren zur herstellung von 1,3-disubstituierten 2-nitroguanidinen |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2003518105A JP2003518105A (ja) | 2003-06-03 |
JP2003518105A5 true JP2003518105A5 (ja) | 2010-03-04 |
JP4463461B2 JP4463461B2 (ja) | 2010-05-19 |
Family
ID=7933521
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001547071A Expired - Fee Related JP4463461B2 (ja) | 1999-12-21 | 2000-12-08 | 1,3−二置換2−ニトログアニジンの製造方法 |
Country Status (20)
Country | Link |
---|---|
US (1) | US6528651B1 (ja) |
EP (1) | EP1242390B1 (ja) |
JP (1) | JP4463461B2 (ja) |
KR (1) | KR100792810B1 (ja) |
CN (1) | CN1243739C (ja) |
AT (1) | ATE273289T1 (ja) |
AU (1) | AU2007601A (ja) |
BR (1) | BR0016521B1 (ja) |
CA (1) | CA2394611C (ja) |
CZ (1) | CZ301629B6 (ja) |
DE (2) | DE19961604A1 (ja) |
DK (1) | DK1242390T3 (ja) |
ES (1) | ES2223624T3 (ja) |
HU (1) | HU230147B1 (ja) |
IL (2) | IL149748A0 (ja) |
IN (1) | IN189560B (ja) |
MX (1) | MXPA02006159A (ja) |
TW (1) | TWI261054B (ja) |
WO (1) | WO2001046160A1 (ja) |
ZA (1) | ZA200203983B (ja) |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5238949A (en) | 1988-11-29 | 1993-08-24 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro pyridyl compounds |
JP2779403B2 (ja) | 1988-11-29 | 1998-07-23 | 日本バイエルアグロケム株式会社 | 殺虫性ニトロ化合物 |
IE71183B1 (en) | 1988-12-27 | 1997-01-29 | Takeda Chemical Industries Ltd | Guanidine derivatives their production and insecticides |
DK0383091T3 (da) | 1989-02-13 | 1994-02-07 | Bayer Agrochem Kk | Insecticidt virksomme nitroforbindelser |
US5204359A (en) | 1989-02-13 | 1993-04-20 | Nihon Bayer Agrochem K.K. | Insecticidally active nitro compounds |
JP2610988B2 (ja) | 1989-03-09 | 1997-05-14 | 日本バイエルアグロケム 株式会社 | 新規ヘテロ環式化合物及び殺虫剤 |
US6187773B1 (en) | 1989-11-10 | 2001-02-13 | Agro-Kanesho Co., Ltd. | Hexahydrotriazine compounds and insecticides |
JPH0674249B2 (ja) | 1990-04-05 | 1994-09-21 | アグロカネショウ株式会社 | 置換ニトログアニジン類の製造法 |
IL99576A0 (en) | 1990-10-05 | 1992-08-18 | Ciba Geigy Ag | Triazacyclohexane derivatives |
TW198724B (ja) * | 1990-10-24 | 1993-01-21 | Ciba Geigy Ag | |
JPH1067766A (ja) | 1996-06-21 | 1998-03-10 | Mitsui Petrochem Ind Ltd | テトラヒドロフラン誘導体の製造法 |
JPH10147580A (ja) | 1996-09-17 | 1998-06-02 | Mitsui Chem Inc | テトラヒドロフラン誘導体の製造法 |
DE19712411A1 (de) | 1997-03-25 | 1998-10-01 | Bayer Ag | Verfahren zur Herstellung von 1,3-disubstituierten 2-Nitroguanidinen |
US6118007A (en) * | 1997-03-31 | 2000-09-12 | Mitsui Chemicals, Inc. | Preparation process of nitroguanidine derivatives |
ID24319A (id) | 1997-08-20 | 2000-07-13 | Novartis Ag | Metode pembuatan turunan2-nitroguanidin tersubstitusi |
-
1999
- 1999-12-21 DE DE19961604A patent/DE19961604A1/de not_active Withdrawn
-
2000
- 2000-11-29 IN IN1081MU2000 patent/IN189560B/en unknown
- 2000-12-08 BR BRPI0016521-2A patent/BR0016521B1/pt not_active IP Right Cessation
- 2000-12-08 CN CNB008174288A patent/CN1243739C/zh not_active Expired - Fee Related
- 2000-12-08 JP JP2001547071A patent/JP4463461B2/ja not_active Expired - Fee Related
- 2000-12-08 CZ CZ20022204A patent/CZ301629B6/cs not_active IP Right Cessation
- 2000-12-08 AU AU20076/01A patent/AU2007601A/en not_active Abandoned
- 2000-12-08 ES ES00983274T patent/ES2223624T3/es not_active Expired - Lifetime
- 2000-12-08 CA CA2394611A patent/CA2394611C/en not_active Expired - Lifetime
- 2000-12-08 KR KR1020027006841A patent/KR100792810B1/ko active IP Right Grant
- 2000-12-08 DK DK00983274T patent/DK1242390T3/da active
- 2000-12-08 AT AT00983274T patent/ATE273289T1/de active
- 2000-12-08 EP EP00983274A patent/EP1242390B1/de not_active Expired - Lifetime
- 2000-12-08 MX MXPA02006159A patent/MXPA02006159A/es active IP Right Grant
- 2000-12-08 WO PCT/EP2000/012495 patent/WO2001046160A1/de active IP Right Grant
- 2000-12-08 US US10/149,891 patent/US6528651B1/en not_active Expired - Lifetime
- 2000-12-08 IL IL14974800A patent/IL149748A0/xx active IP Right Grant
- 2000-12-08 DE DE50007410T patent/DE50007410D1/de not_active Expired - Lifetime
- 2000-12-08 HU HU0300192A patent/HU230147B1/hu not_active IP Right Cessation
- 2000-12-20 TW TW089127310A patent/TWI261054B/zh not_active IP Right Cessation
-
2002
- 2002-05-20 ZA ZA200203983A patent/ZA200203983B/en unknown
- 2002-05-20 IL IL149748A patent/IL149748A/en unknown
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