FR2121394A1 - Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé. - Google Patents

Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé.

Info

Publication number
FR2121394A1
FR2121394A1 FR7100498A FR7100498A FR2121394A1 FR 2121394 A1 FR2121394 A1 FR 2121394A1 FR 7100498 A FR7100498 A FR 7100498A FR 7100498 A FR7100498 A FR 7100498A FR 2121394 A1 FR2121394 A1 FR 2121394A1
Authority
FR
France
Prior art keywords
inters
tranquillisers
antiinflammatories
analgesics
fungicides
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
Application number
FR7100498A
Other languages
English (en)
Other versions
FR2121394B1 (fr
Inventor
Jacques Bourdais
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bpifrance Financement SA
Original Assignee
Agence National de Valorisation de la Recherche ANVAR
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Agence National de Valorisation de la Recherche ANVAR filed Critical Agence National de Valorisation de la Recherche ANVAR
Priority to FR7100498A priority Critical patent/FR2121394A1/fr
Publication of FR2121394A1 publication Critical patent/FR2121394A1/fr
Application granted granted Critical
Publication of FR2121394B1 publication Critical patent/FR2121394B1/fr
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
FR7100498A 1971-01-08 1971-01-08 Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé. Granted FR2121394A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR7100498A FR2121394A1 (fr) 1971-01-08 1971-01-08 Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7100498A FR2121394A1 (fr) 1971-01-08 1971-01-08 Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé.

Publications (2)

Publication Number Publication Date
FR2121394A1 true FR2121394A1 (fr) 1972-08-25
FR2121394B1 FR2121394B1 (fr) 1974-03-22

Family

ID=9069997

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7100498A Granted FR2121394A1 (fr) 1971-01-08 1971-01-08 Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé.

Country Status (1)

Country Link
FR (1) FR2121394A1 (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5189041A (en) * 1990-11-16 1993-02-23 Syntex (U.S.A.) Inc. Tricyclic 5-ht3 receptor antagonists
WO1999041239A1 (fr) * 1998-02-10 1999-08-19 Novartis Ag Inhibiteurs de lymphocytes b
WO2003082860A1 (fr) * 2002-04-01 2003-10-09 Nissan Chemical Industries, Ltd. Procedes de production de compose indole
WO2007095561A3 (fr) * 2006-02-15 2007-10-11 Allergan Inc Composes amide d'acide indole-3-carboxylique, ester, thioamide et ester de thiol porteurs de groupes aryl ou heteroaryl presentant une activite biologique antagoniste sur le recepteur sphingosine-1-phosphate (s1p)
US7338956B2 (en) 2002-08-07 2008-03-04 Sanofi-Aventis Deutschland Gmbh Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
WO2008089015A1 (fr) 2007-01-11 2008-07-24 Allergan, Inc. Composé amide d'acide indole-3-carboxylique 6-substitué ayant une activité biologique d'antagoniste du récepteur de sphingosine-1-phosphate (s1p)
WO2009117335A2 (fr) * 2008-03-17 2009-09-24 Allergan, Inc. Inhibiteurs des récepteurs s1 p3 pour le traitement de l'inflammation
US7737173B2 (en) 2006-02-15 2010-06-15 Allergan, Inc. Indole-3-carboxylic acid amide, ester, thioamide and thiol ester compounds bearing aryl or heteroaryl groups having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
US8524917B2 (en) 2007-01-11 2013-09-03 Allergan, Inc. 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5189041A (en) * 1990-11-16 1993-02-23 Syntex (U.S.A.) Inc. Tricyclic 5-ht3 receptor antagonists
WO1999041239A1 (fr) * 1998-02-10 1999-08-19 Novartis Ag Inhibiteurs de lymphocytes b
WO2003082860A1 (fr) * 2002-04-01 2003-10-09 Nissan Chemical Industries, Ltd. Procedes de production de compose indole
US7338956B2 (en) 2002-08-07 2008-03-04 Sanofi-Aventis Deutschland Gmbh Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
WO2007095561A3 (fr) * 2006-02-15 2007-10-11 Allergan Inc Composes amide d'acide indole-3-carboxylique, ester, thioamide et ester de thiol porteurs de groupes aryl ou heteroaryl presentant une activite biologique antagoniste sur le recepteur sphingosine-1-phosphate (s1p)
JP2009526863A (ja) * 2006-02-15 2009-07-23 アラーガン、インコーポレイテッド スフィンゴシン−１−リン酸（ｓ１ｐ）受容体アンタゴニスト生物学的活性を有するアリールまたはヘテロアリール基を持つインドール−３−カルボン酸アミド、エステル、チオアミドおよびチオールエステル化合物
US7737173B2 (en) 2006-02-15 2010-06-15 Allergan, Inc. Indole-3-carboxylic acid amide, ester, thioamide and thiol ester compounds bearing aryl or heteroaryl groups having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
WO2008089015A1 (fr) 2007-01-11 2008-07-24 Allergan, Inc. Composé amide d'acide indole-3-carboxylique 6-substitué ayant une activité biologique d'antagoniste du récepteur de sphingosine-1-phosphate (s1p)
JP2010515750A (ja) * 2007-01-11 2010-05-13 アラーガン インコーポレイテッド スフィンゴシン−１−ホスフェート（ｓ１ｐ）受容体アンタゴニスト生物活性を有する６−置換インドール−３−カルボン酸アミド化合物
US8524917B2 (en) 2007-01-11 2013-09-03 Allergan, Inc. 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
WO2009117335A2 (fr) * 2008-03-17 2009-09-24 Allergan, Inc. Inhibiteurs des récepteurs s1 p3 pour le traitement de l'inflammation
WO2009117335A3 (fr) * 2008-03-17 2009-12-10 Allergan, Inc. Inhibiteurs des récepteurs s1 p3 pour le traitement de l'inflammation

Also Published As

Publication number Publication date
FR2121394B1 (fr) 1974-03-22

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