JP2005035972A5 - - Google Patents

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JP2005035972A5
JP2005035972A5 JP2004084225A JP2004084225A JP2005035972A5 JP 2005035972 A5 JP2005035972 A5 JP 2005035972A5 JP 2004084225 A JP2004084225 A JP 2004084225A JP 2004084225 A JP2004084225 A JP 2004084225A JP 2005035972 A5 JP2005035972 A5 JP 2005035972A5
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Japan
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general formula
compound represented
nitrogen
substituted
containing heterocyclic
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JP2004084225A
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Japanese (ja)
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JP4608922B2 (en
JP2005035972A (en
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Publication of JP2005035972A5 publication Critical patent/JP2005035972A5/ja
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Description

Figure 2005035972
Figure 2005035972

Claims (2)

一般式(1)で表される1−置換含窒素複素環化合物が一般式(6)
Figure 2005035972
(ここでR1、R2は前記と同様。)で表される1−置換−3−アミノピロリジン誘導体であり、一般式(4)で表される含窒素複素環化合物が一般式(7)
Figure 2005035972
(ここでR1、R2、R3は前記と同様。)で表される3−置換−アミノピロリジン誘導体であることを特徴とする請求項1〜5のいずれか1項記載の含窒素複素環化合物の製造方法。
The 1-substituted nitrogen-containing heterocyclic compound represented by the general formula (1) is a compound represented by the general formula (6)
Figure 2005035972
(Wherein R 1 and R 2 are as defined above) is a 1-substituted 3-aminopyrrolidine derivative, and the nitrogen-containing heterocyclic compound represented by the general formula (4) is a compound represented by the general formula (7)
Figure 2005035972
The nitrogen-containing complex according to any one of claims 1 to 5, which is a 3-substituted-aminopyrrolidine derivative represented by (wherein R 1 , R 2 and R 3 are as defined above). Method for producing a ring compound
一般式(4)で表される含窒素複素環化合物が一般式(7)
Figure 2005035972
(ここでR1、R2、R3は前記と同様。)で表される3−置換−アミノピロリジン誘導体であり、一般式(5)で表される含窒素複素環化合物が一般式(8)
Figure 2005035972
(ここでR2、R3は前記と同様。)で表される3−置換−アミノピロリジン誘導体であることを特徴とする請求項7または8記載の含窒素複素環化合物の製造方法。
The nitrogen-containing heterocyclic compound represented by the general formula (4) is a compound represented by the general formula (7)
Figure 2005035972
(Wherein R 1 , R 2 and R 3 are as defined above) is a 3-substituted-aminopyrrolidine derivative, and the nitrogen-containing heterocyclic compound represented by the general formula (5) is a compound represented by the general formula (8) )
Figure 2005035972
The method for producing a nitrogen-containing heterocyclic compound according to claim 7 or 8, which is a 3-substituted-aminopyrrolidine derivative represented by (wherein R 2 and R 3 are as defined above).
JP2004084225A 2003-06-27 2004-03-23 Method for producing nitrogen-containing heterocyclic compound Expired - Lifetime JP4608922B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2004084225A JP4608922B2 (en) 2003-06-27 2004-03-23 Method for producing nitrogen-containing heterocyclic compound

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2003184058 2003-06-27
JP2004084225A JP4608922B2 (en) 2003-06-27 2004-03-23 Method for producing nitrogen-containing heterocyclic compound

Publications (3)

Publication Number Publication Date
JP2005035972A JP2005035972A (en) 2005-02-10
JP2005035972A5 true JP2005035972A5 (en) 2007-05-24
JP4608922B2 JP4608922B2 (en) 2011-01-12

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JP2004084225A Expired - Lifetime JP4608922B2 (en) 2003-06-27 2004-03-23 Method for producing nitrogen-containing heterocyclic compound

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Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3906365A1 (en) * 1988-07-15 1990-01-18 Bayer Ag 7- (1-PYRROLIDINYL) -3-CHINOLONE AND NAPHTHYRIDONE CARBOXYLIC ACID DERIVATIVES, METHOD AND SUBSTITUTED (OXA) DIAZABICYCLOOCTANES AND NONANESE AS INTERMEDIATE PRODUCTS, AND ANTIBACTERIAL AGENTS AND FOOD ADDITIVES CONTAINING THEM
JP2995704B2 (en) * 1989-02-17 1999-12-27 東京化成工業株式会社 Method for producing optically active 1H-3-aminopyrrolidine compound
US5347017A (en) * 1993-07-07 1994-09-13 Warner-Lambert Company Process for chiral 3-(1-amino-1,1-bisalkylmethyl)-1-substituted-pyrrolidines

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